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Een onderzoek waarin de combinatie van dasatinib en chemotherapiebehandeling met of zonder blinatumomab wordt vergeleken bij kinderen, adolescenten en jongvolwassenen met Philadelphia chromosoompositieve (Ph+) of Philadelphia chromosoomachtige (Ph-achtige) ABL-klasse B-cel acute lymfoblastische leukemie (B -ALLE)

24 oktober 2026 bijgewerkt door: National Cancer Institute (NCI)

Een gerandomiseerd internationaal fase 3-onderzoek naar imatinib en chemotherapie met of zonder blinatumomab bij patiënten met nieuw gediagnosticeerde Philadelphia-chromosoompositieve of Philadelphia-chromosoomachtige ABL-klasse B-cel acute lymfoblastische leukemie

This pilot trial assesses the effect of the combination of blinatumomab with dasatinib or imatinib and standard chemotherapy for treating patients with Philadelphia chromosome positive (Ph+) or ABL-class Philadelphia chromosome-like (Ph-like) B-Cell acute lymphoblastic leukemia (B-ALL). Blinatumomab is a bispecific antibody that binds to two different proteins-one on the surface of cancer cells and one on the surface of cells in the immune system. An antibody is a protein made by the immune system to help fight infections and other harmful processes/cells/molecules. Blinatumomab may bind to the cancer cell and a T cell (which plays a key role in the immune system's fighting response) at the same time. Blinatumomab may strengthen the immune system's ability to fight cancer cells by activating the body's own immune cells to destroy the tumor. Dasatinib and imatinib are in a class of medications called tyrosine kinase inhibitors. They work by blocking the action of an abnormal protein that signals cancer cells to multiply, which may help keep cancer cells from growing. Giving blinatumomab and dasatinib or imatinib in combination with standard chemotherapy may work better in treating patients with Ph+ or Ph-like ABL-class B-ALL than dasatinib or imatinib with chemotherapy.

Studie Overzicht

Toestand

Werving

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

PRIMARY OBJECTIVES:

I. To estimate the 3-year event free survival (EFS) of children, adolescents, and young adults <25 years old with newly-diagnosed Ph+ (BCR::ABL1-rearranged) B- ALL who are treated with a modified Berlin-Frankfurt-Münster (mBFM) chemotherapy backbone that incorporates three cycles of blinatumomab without traditional consolidation chemotherapy in combination with continuous dasatinib.

II. To estimate the 3-year EFS of children, adolescents, and young adults <25 years old with newly-diagnosed ABL-class Ph-like B-ALL who are treated with a modified BFM chemotherapy backbone that incorporates three cycles of blinatumomab without traditional consolidation chemotherapy in combination with continuous imatinib for those with PDGFRB gene fusions or dasatinib for those without PDGFRB gene fusions.

III. To describe the safety and toxicity profile (infections, mucositis, neurotoxicity, cytokine release syndrome, hypogammaglobulinemia, therapy delays > 14 days, and treatment-related mortality) for patients with Ph+ or ABL-class Ph-like B-ALL treated on this novel chemo-immunotherapy backbone with continuous tyrosine kinase inhibitor (TKI).

SECONDARY OBJECTIVES:

I. To estimate the 3-year overall survival (OS) of patients with Ph+ and ABL-class Ph-like B-ALL, respectively.

II. To estimate the 3-year EFS, disease-free survival (DFS), cumulative incidence rates (CIR) of relapse, and treatment related mortality (TRM), and OS of patients with ABL-class Ph-like B-ALL stratified by their underlying ABL-class fusion subtypes.

III. To describe rates of end of consolidation (EOC)/timepoint 2 (TP2) minimal residual disease (MRD) negativity defined as <1x10-4 or <0.01% for patients with Ph+ B-ALL.

IV. To describe rates of EOC/TP2 MRD negativity defined as <1x10-4 or <0.01% for patients with ABL-class Ph-like B-ALL collectively and based on their ABL-class fusion subtypes.

EXPLORATORY OBJECTIVES:

I. To describe rates of end of induction (EOI)/timepoint 1 (TP1) bone marrow MRD negativity defined as <1x10-4 or <0.01% with the introduction of the relevant TKI during Induction for patients with Ph+ and ABL-class Ph-like B-ALL, respectively.

II. To describe the outcomes of patients with Ph+ and ABL-class Ph-like B-ALL who are removed from protocol therapy due to Consolidation Failure.

III. To describe the percentage of patients with Ph+ and ABL-class Ph-like B-ALL who continue TKI beyond protocol-prescribed therapy and their outcomes.

IV. To describe the impact of MRD by next-generation sequencing (NGS) at End of Consolidation on outcomes for patients with Ph+ and ABL-class Ph-like B-ALL.

V. To describe the clinical characteristics and outcomes of patients with chronic myeloid leukemia-like biology.

VI. To describe the immune function of patients with Ph+ and ABL-class Ph-like B-ALL pre- and post-blinatumomab plus TKI and correlate with treatment response.

VII. To describe the TKI levels in the plasma and cerebrospinal fluid of children with Ph+ and ABL-class Ph-like B-ALL over the treatment course and correlate with outcome VIII. To describe the impact of TKIs and high-dose methotrexate interaction and identify clinical and biologic factors influencing methotrexate clearance.

OUTLINE:

STRATUM I (PH+ B-ALL PATIENTS):

INDUCTION PART I: Patients receive induction chemotherapy on days 1-14 as per standard of care (SOC).

INDUCTION PART II: Patients receive dasatinib PO once daily (QD) on days 15-29, daunorubicin intravenously (IV) over 15 minutes on days 15 and 22, prednisolone or prednisone PO twice daily (BID) on days 15-28, vincristine IV on days 15 and 22, methotrexate intrathecally (IT) on days 15, 22, and 29, and cytarabine IT on days 18 and 25 if central nervous system (CNS)-3 at study entry.

BLINATUMOMAB BLOCK I: Patients receive dexamethasone PO or intravenously (IV) on day 1, blinatumomab IV on days 1-28, dasatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study. Patients may undergo radiation therapy in 12 QD fractions.

BLINATUMOMAB BLOCK II: Patients receive dexamethasone PO or IV on day 1, blinatumomab IV on days 1-28, dasatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study.

INTERIM MAINTENANCE I: Patients receive dasatinib PO QD until the end of interim maintenance I, mercaptopurine PO QD on days 1-56, vincristine IV on days 8, 22, 36, and 50, methotrexate IT on days 8 and 36, high-dose methotrexate IV over 24 hours on days 8, 22, 36 and 50, and leucovorin PO or IV on days 10, 11, 24, 25, 38, 39, 52 and 53 over 9 weeks on study.

BLINATUMOMAB BLOCK III: Patients receive blinatumomab IV on days 1-28, dasatinib PO QD on days 1-35, and methotrexate IT on day 1 over 5 weeks on study.

DELAYED INTENSIFICATION PART I: Patients receive dasatinib PO QD on days 1-28, methotrexate IT on day 1, dexamethasone PO or IV on days 1-7 and 15-21, doxorubicin IV over 15 minutes on days 1, 8, and 15, vincristine IV on days 1, 8, and 15, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on day 4 over 4 weeks on study.

DELAYED INTENSIFICATION PART II: Patients receive dasatinib PO QD on day 29 until the end of delayed intensification part II, cyclophosphamide IV over 60 minutes on day 29, cytarabine IV over 30 minutes on days 29-32 and 36-39, methotrexate IT on days 29 and 36, thioguanine PO on days 29-42, pegaspargase IV or calaspargase pegol on day 43 and vincristine IV on days 43 and 50 over 5 weeks on study.

INTERIM MAINTENANCE PART II: Patients receive dasatinib PO QD on day 1 until the end of interim maintenance part II, methotrexate IV on days 1, 11, 21, 31, and 41, vincristine IV on 1, 11, 21, 31, and 41, methotrexate IT on days 1 and 31, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on days 2, 22 or 23 over 8 weeks on study.

MAINTENANCE CYCLES I-II: Patients receive dasatinib PO QD on days 1-84, methotrexate IT on days 1 and 29, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study.

MAINTENANCE CYCLES III AND SUBSEQUENT CYCLES: Patients receive dasatinib PO QD on days 1-84, methotrexate IT on day 1, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study. Cycles repeat every 12 weeks for 2 years from the start of Induction therapy in the absence of disease progression or unacceptable toxicity.

STRATUM II (PDGFRB ABL-CLASS FUSIONS):

BLINATUMOMAB BLOCK I: Patients receive dexamethasone PO or IV on day 1, blinatumomab IV on days 1-28, imatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study. Patients may undergo radiation therapy in 12 QD fractions.

BLINATUMOMAB BLOCK II: Patients receive dexamethasone PO or IV on day 1, blinatumomab IV on days 1-28, imatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study.

INTERIM MAINTENANCE I: Patients receive imatinib PO QD until the end of interim maintenance I, mercaptopurine PO QD on days 1-56, vincristine IV on days 8, 22, 36, and 50, methotrexate IT on days 8 and 36, high-dose methotrexate IV over 24 hours on days 8, 22, 36 and 50, and leucovorin PO or IV on days 10, 11, 24, 25, 38, 39, 52 and 53 over 9 weeks on study.

BLINATUMOMAB BLOCK III: Patients receive blinatumomab IV on days 1-28, imatinib PO QD on days 1-35, and methotrexate IT on day 1 over 5 weeks on study.

DELAYED INTENSIFICATION PART I: Patients receive imatinib PO QD on days 1-28, methotrexate IT on day 1, dexamethasone PO or IV on days 1-7 and 15-21, doxorubicin IV over 15 minutes on days 1, 8, and 15, vincristine IV on days 1, 8, and 15, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on day 4 over 9 weeks on study.

DELAYED INTENSIFICATION PART II: Patients receive imatinib PO QD on day 29 until the end of Delayed Intensification part II, cyclophosphamide IV over 30-60 minutes on day 29, cytarabine IV over 30 minutes on days 29-32 and 36-39, methotrexate IT on days 29 and 36, thioguanine PO on days 29-42, and pegaspargase IV or calaspargase pegol IV on day 43, and vincristine IV on days 43 and 50 over 5 weeks on study.

INTERIM MAINTENANCE II: Patients receive imatinib PO QD until the end of interim maintenance II, methotrexate IV and vincristine IV on days 1, 11, 21, 31 and 41, methotrexate IT on days 1 and 31, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on days 2, 22 or 23 over 8 weeks on study.

MAINTENANCE CYCLES I-II: Patients receive imatinib PO QD on days 1-84, methotrexate IT on days 1 and 29, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study.

MAINTENANCE CYCLES III AND SUBSEQUENT CYCLES: Patients receive imatinib PO QD on days 1-84, methotrexate IT on day 1, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study. Cycles repeat every 12 weeks for 2 years from the start of Induction therapy in the absence of disease progression or unacceptable toxicity.

STRATUM III (NON-PDGFRB ABL-CLASS FUSIONS):

BLINATUMOMAB BLOCK I: Patients receive dexamethasone PO or IV on day 1, blinatumomab IV on days 1-28, dasatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study. Patients may undergo radiation therapy in 12 QD fractions.

BLINATUMOMAB BLOCK II: Patients receive dexamethasone PO or IV on day 1, blinatumomab IV on days 1-28, dasatinib PO on days 1-35, and methotrexate IT on days 1 and 15 over 5 weeks on study.

INTERIM MAINTENANCE I: Patients receive dasatinib PO QD until the end of interim maintenance I, mercaptopurine PO QD on days 1-56, vincristine IV on days 8, 22, 36, and 50, methotrexate IT on days 8 and 36, high-dose methotrexate IV over 24 hours on days 8, 22, 36 and 50, and leucovorin PO or IV on days 10, 11, 24, 25, 38, 39, 52 and 53 over 9 weeks on study.

BLINATUMOMAB BLOCK III: Patients receive blinatumomab IV on days 1-28, dasatinib PO on days 1-35, and methotrexate IT on day 1 over 5 weeks on study.

DELAYED INTENSIFICATION PART I: Patients receive dasatinib PO QD on days 1-28, methotrexate IT on day 1, dexamethasone PO or IV on days 1-7 and 15-21, doxorubicin IV over 15 minutes on days 1, 8, and 15, vincristine IV on days 1, 8, and 15, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on day 4 over 4 weeks on study.

DELAYED INTENSIFICATION PART II: Patients receive dasatinib PO QD and methotrexate IT on day 29 until the end of Delayed Intensification part II, cyclophosphamide IV over 30-60 minutes on day 29, cytarabine IV over 30 minutes on days 29-32 and 36-39, methotrexate IT on days 29 and 36, thioguanine PO on days 29-42, pegaspargase IV or calaspargase pegol on day 43 and vincristine IV on days 43 and 50 over 5 weeks on study.

INTERIM MAINTENANCE II: Patients receive dasatinib PO QD until the end of interim maintenance II, methotrexate IV and vincristine IV on days 1, 11, 21, 31 and 41, methotrexate IT on days 1 and 31, and pegaspargase IV or calaspargase pegol IV over 1-2 hours on days 2, 22 or 23 over 8 weeks on study.

MAINTENANCE CYCLES I-II: Patients receive dasatinib PO QD on days 1-84, methotrexate IT on days 1 and 29, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study.

MAINTENANCE CYCLES III AND SUBSEQUENT CYCLES: Patients receive dasatinib PO QD on days 1-84, methotrexate IT on day 1, dexamethasone PO BID or IV on days 1-5, 29-33, and 57-61, mercaptopurine PO on days 1-84, vincristine IV on days 1, 29 and 57, and methotrexate PO on days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78 on study. Cycles repeat every 12 weeks for 2 years from the start of Induction therapy in the absence of disease progression or unacceptable toxicity.

All patients undergo echocardiography (ECHO) or multigated acquisition scan (MUGA) during screening. Patients also undergo blood and cerebrospinal fluid (CSF) sample collection and bone marrow biopsy throughout the study and as clinically indicated on study.

Studietype

Ingrijpend

Inschrijving (Geschat)

222

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • Australië
    • New South Wales
      • Hunter Regional Mail Centre, New South Wales, Australië, 2310
        • Werving
        • John Hunter Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: (02) 4985 5180
        • Hoofdonderzoeker:
          • Kristy McCarthy
    • Queensland
      • South Brisbane, Queensland, Australië, 4101
        • Werving
        • Queensland Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 61 7 3068 1111
        • Hoofdonderzoeker:
          • Christopher J. Fraser
    • Victoria
      • Parkville, Victoria, Australië, 3052
        • Werving
        • Royal Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Stacie S. Wang
    • Western Australia
      • Perth, Western Australia, Australië, 6009
  • Canada
      • Québec, Canada, G1V 4G2
        • Werving
        • CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL)
        • Hoofdonderzoeker:
          • Bruno Michon
        • Contact:
    • Alberta
      • Calgary, Alberta, Canada, T3B 6A8
        • Geschorst
        • Alberta Children's Hospital
      • Edmonton, Alberta, Canada, T6G 2B7
        • Werving
        • University of Alberta Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Sarah J. McKillop
    • British Columbia
      • Vancouver, British Columbia, Canada, V6H 3V4
        • Geschorst
        • British Columbia Children's Hospital
    • Manitoba
      • Winnipeg, Manitoba, Canada, R3E 0V9
        • Werving
        • CancerCare Manitoba
        • Contact:
        • Hoofdonderzoeker:
          • Stephanie M. Villeneuve
    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3K 6R8
        • Werving
        • IWK Health Centre
        • Contact:
        • Hoofdonderzoeker:
          • Chelsea Ash
    • Ontario
      • Hamilton, Ontario, Canada, L8N 3Z5
        • Werving
        • McMaster Children's Hospital at Hamilton Health Sciences
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 905-521-2100
        • Hoofdonderzoeker:
          • Uma H. Athale
      • Toronto, Ontario, Canada, M5G 1X8
        • Werving
        • Hospital for Sick Children
        • Hoofdonderzoeker:
          • Sumit Gupta
        • Contact:
    • Quebec
      • Montreal, Quebec, Canada, H3H 1P3
        • Werving
        • The Montreal Children's Hospital of the MUHC
        • Contact:
        • Hoofdonderzoeker:
          • Stephanie Mourad
      • Montreal, Quebec, Canada, H3T 1C5
        • Werving
        • Centre Hospitalier Universitaire Sainte-Justine
        • Hoofdonderzoeker:
          • Monia Marzouki
        • Contact:
      • Sherbrooke, Quebec, Canada, J1H 5N4
        • Werving
        • Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
        • Contact:
        • Hoofdonderzoeker:
          • Stephanie Vairy
  • Puerto Rico
      • San Juan, Puerto Rico, 00926
        • Werving
        • University Pediatric Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 787-474-0333
        • Hoofdonderzoeker:
          • Maria E. Echevarria
  • Verenigde Staten
    • Alabama
      • Birmingham, Alabama, Verenigde Staten, 35233
        • Werving
        • Children's Hospital of Alabama
        • Contact:
        • Hoofdonderzoeker:
          • Matthew A. Kutny
    • Arizona
      • Phoenix, Arizona, Verenigde Staten, 85016
        • Werving
        • Phoenix Childrens Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 602-546-0920
        • Hoofdonderzoeker:
          • Dana B. Salzberg
      • Tucson, Arizona, Verenigde Staten, 85719
        • Werving
        • Banner University Medical Center - Tucson
        • Contact:
        • Hoofdonderzoeker:
          • Monica M. Davini
    • Arkansas
      • Little Rock, Arkansas, Verenigde Staten, 72202-3591
        • Werving
        • Arkansas Children's Hospital
        • Hoofdonderzoeker:
          • Michael W. Bishop
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 501-364-7373
    • California
      • Downey, California, Verenigde Staten, 90242
        • Werving
        • Kaiser Permanente Downey Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 626-564-3455
        • Hoofdonderzoeker:
          • Robert M. Cooper
      • Loma Linda, California, Verenigde Staten, 92354
        • Werving
        • Loma Linda University Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 909-558-4050
        • Hoofdonderzoeker:
          • Albert Kheradpour
      • Long Beach, California, Verenigde Staten, 90806
        • Werving
        • Miller Children's and Women's Hospital Long Beach
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 562-933-5600
        • Hoofdonderzoeker:
          • Jacqueline N. Casillas
      • Los Angeles, California, Verenigde Staten, 90027
        • Werving
        • Children's Hospital Los Angeles
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 323-361-4110
        • Hoofdonderzoeker:
          • Andrew Doan
      • Madera, California, Verenigde Staten, 93636
        • Werving
        • Valley Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Ruetima Titapiwatanakun
      • Oakland, California, Verenigde Staten, 94611
        • Werving
        • Kaiser Permanente-Oakland
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 877-642-4691
          • E-mail: Kpoct@kp.org
        • Hoofdonderzoeker:
          • Aarati V. Rao
      • Oakland, California, Verenigde Staten, 94609
        • Werving
        • UCSF Benioff Children's Hospital Oakland
        • Hoofdonderzoeker:
          • Karen R. Rabin
        • Contact:
      • Orange, California, Verenigde Staten, 92868
        • Werving
        • Children's Hospital of Orange County
        • Contact:
        • Hoofdonderzoeker:
          • Elyssa M. Rubin
      • Palo Alto, California, Verenigde Staten, 94304
        • Werving
        • Lucile Packard Children's Hospital Stanford University
        • Contact:
        • Hoofdonderzoeker:
          • Jay Michael S. Balagtas
      • Sacramento, California, Verenigde Staten, 95817
        • Werving
        • University of California Davis Comprehensive Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 916-734-3089
        • Hoofdonderzoeker:
          • Marcio H. Malogolowkin
      • San Diego, California, Verenigde Staten, 92123
        • Werving
        • Rady Children's Hospital - San Diego
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 858-966-5934
        • Hoofdonderzoeker:
          • William D. Roberts
      • San Francisco, California, Verenigde Staten, 94158
        • Werving
        • UCSF Medical Center-Mission Bay
        • Contact:
        • Hoofdonderzoeker:
          • Karen R. Rabin
    • Colorado
      • Aurora, Colorado, Verenigde Staten, 80045
        • Werving
        • Children's Hospital Colorado
        • Contact:
        • Hoofdonderzoeker:
          • Kelly W. Maloney
    • Connecticut
      • Hartford, Connecticut, Verenigde Staten, 06106
        • Werving
        • Connecticut Children's Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 860-545-9981
        • Hoofdonderzoeker:
          • Michael S. Isakoff
      • New Haven, Connecticut, Verenigde Staten, 06520
        • Werving
        • Yale University
        • Contact:
        • Hoofdonderzoeker:
          • Farzana Pashankar
    • Delaware
      • Wilmington, Delaware, Verenigde Staten, 19803
        • Werving
        • Alfred I duPont Hospital for Children
        • Contact:
        • Hoofdonderzoeker:
          • Emi H. Caywood
    • District of Columbia
      • Washington D.C., District of Columbia, Verenigde Staten, 20010
        • Werving
        • Children's National Medical Center
        • Hoofdonderzoeker:
          • Jeffrey S. Dome
        • Contact:
      • Washington D.C., District of Columbia, Verenigde Staten, 20007
        • Werving
        • MedStar Georgetown University Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 202-444-2223
        • Hoofdonderzoeker:
          • Caileigh Pudela
    • Florida
      • Fort Myers, Florida, Verenigde Staten, 33908
        • Werving
        • Golisano Children's Hospital of Southwest Florida
        • Contact:
        • Hoofdonderzoeker:
          • Emad K. Salman
      • Gainesville, Florida, Verenigde Staten, 32610
        • Werving
        • UF Health Cancer Institute - Gainesville
        • Hoofdonderzoeker:
          • Brian Stover
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 352-273-8010
      • Hollywood, Florida, Verenigde Staten, 33021
        • Werving
        • Memorial Regional Hospital/Joe DiMaggio Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 954-265-1847
          • E-mail: OHR@mhs.net
        • Hoofdonderzoeker:
          • Iftikhar Hanif
      • Jacksonville, Florida, Verenigde Staten, 32207
        • Werving
        • Nemours Children's Clinic-Jacksonville
        • Contact:
        • Hoofdonderzoeker:
          • Emi H. Caywood
      • Miami, Florida, Verenigde Staten, 33136
        • Werving
        • University of Miami Miller School of Medicine-Sylvester Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 305-243-2647
        • Hoofdonderzoeker:
          • Julio C. Barredo
      • Orlando, Florida, Verenigde Staten, 32806
        • Werving
        • Arnold Palmer Hospital for Children
        • Contact:
        • Hoofdonderzoeker:
          • Zhongbo Hu
      • Orlando, Florida, Verenigde Staten, 32827
        • Werving
        • Nemours Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Emi H. Caywood
      • Orlando, Florida, Verenigde Staten, 32803
        • Werving
        • AdventHealth Orlando
        • Contact:
        • Hoofdonderzoeker:
          • Fouad M. Hajjar
      • Pensacola, Florida, Verenigde Staten, 32504
      • St. Petersburg, Florida, Verenigde Staten, 33701
        • Werving
        • Johns Hopkins All Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Jennifer B. Dean
      • Tampa, Florida, Verenigde Staten, 33607
        • Werving
        • Saint Joseph's Hospital/Children's Hospital-Tampa
        • Contact:
        • Hoofdonderzoeker:
          • Don E. Eslin
      • West Palm Beach, Florida, Verenigde Staten, 33407
        • Werving
        • Saint Mary's Medical Center
        • Hoofdonderzoeker:
          • Matthew D. Ramirez
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 561-822-4745
    • Georgia
      • Atlanta, Georgia, Verenigde Staten, 30329
        • Werving
        • Children's Healthcare of Atlanta - Arthur M Blank Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Lauren Raney
      • Augusta, Georgia, Verenigde Staten, 30912
        • Werving
        • Augusta University Medical Center
        • Contact:
        • Hoofdonderzoeker:
          • Colleen H. McDonough
      • Macon, Georgia, Verenigde Staten, 31201
      • Savannah, Georgia, Verenigde Staten, 31404
        • Werving
        • Memorial Health University Medical Center
        • Contact:
        • Hoofdonderzoeker:
          • James N. Yarnall
    • Hawaii
      • Honolulu, Hawaii, Verenigde Staten, 96826
        • Werving
        • Kapiolani Medical Center for Women and Children
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 808-983-6090
        • Hoofdonderzoeker:
          • Wade T. Kyono
    • Idaho
      • Boise, Idaho, Verenigde Staten, 83712
        • Werving
        • Saint Luke's Cancer Institute - Boise
        • Hoofdonderzoeker:
          • Martha M. Pacheco
        • Contact:
    • Illinois
      • Chicago, Illinois, Verenigde Staten, 60611
        • Werving
        • Lurie Children's Hospital-Chicago
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 773-880-4562
        • Hoofdonderzoeker:
          • Loretta S. Li
      • Chicago, Illinois, Verenigde Staten, 60637
        • Werving
        • University of Chicago Comprehensive Cancer Center
        • Contact:
        • Hoofdonderzoeker:
          • Gabrielle Lapping-Carr
      • Chicago, Illinois, Verenigde Staten, 60612
        • Werving
        • University of Illinois
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 312-355-3046
        • Hoofdonderzoeker:
          • Dipti S. Dighe
      • Oak Lawn, Illinois, Verenigde Staten, 60453
        • Werving
        • Advocate Children's Hospital-Oak Lawn
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 847-723-7570
        • Hoofdonderzoeker:
          • Rebecca E. McFall
      • Park Ridge, Illinois, Verenigde Staten, 60068
      • Peoria, Illinois, Verenigde Staten, 61637
      • Springfield, Illinois, Verenigde Staten, 62702
        • Werving
        • Southern Illinois University School of Medicine
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 217-545-7929
        • Hoofdonderzoeker:
          • Gregory P. Brandt
    • Indiana
      • Indianapolis, Indiana, Verenigde Staten, 46202
        • Werving
        • Riley Hospital for Children
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-248-1199
        • Hoofdonderzoeker:
          • Sandeep Batra
      • Indianapolis, Indiana, Verenigde Staten, 46260
        • Werving
        • Ascension Saint Vincent Indianapolis Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Bassem I. Razzouk
    • Iowa
      • Des Moines, Iowa, Verenigde Staten, 50309
        • Werving
        • Blank Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Samantha L. Mallory
      • Iowa City, Iowa, Verenigde Staten, 52242
        • Werving
        • University of Iowa/Holden Comprehensive Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-237-1225
        • Hoofdonderzoeker:
          • Andrew P. Groves
    • Kentucky
      • Lexington, Kentucky, Verenigde Staten, 40536
        • Werving
        • University of Kentucky/Markey Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 859-257-3379
        • Hoofdonderzoeker:
          • James T. Badgett
      • Louisville, Kentucky, Verenigde Staten, 40202
        • Werving
        • Norton Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Michael J. Ferguson
    • Louisiana
      • New Orleans, Louisiana, Verenigde Staten, 70118
        • Werving
        • Children's Hospital New Orleans
        • Hoofdonderzoeker:
          • Maria C. Velez-Yanguas
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 504-894-5377
      • New Orleans, Louisiana, Verenigde Staten, 70121
        • Werving
        • Ochsner Medical Center Jefferson
        • Contact:
        • Hoofdonderzoeker:
          • Craig Lotterman
    • Maine
      • Scarborough, Maine, Verenigde Staten, 04074
        • Werving
        • Maine Children's Cancer Program
        • Hoofdonderzoeker:
          • Eric C. Larsen
        • Contact:
    • Maryland
      • Baltimore, Maryland, Verenigde Staten, 21287
        • Werving
        • Johns Hopkins University/Sidney Kimmel Cancer Center
        • Hoofdonderzoeker:
          • Stacy L. Cooper
        • Contact:
      • Baltimore, Maryland, Verenigde Staten, 21215
        • Werving
        • Sinai Hospital of Baltimore
        • Hoofdonderzoeker:
          • Jason M. Fixler
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 410-601-9083
      • Bethesda, Maryland, Verenigde Staten, 20889-5600
        • Werving
        • Walter Reed National Military Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 301-319-2100
        • Hoofdonderzoeker:
          • Kip R. Hartman
    • Massachusetts
      • Boston, Massachusetts, Verenigde Staten, 02215
        • Werving
        • Dana-Farber Cancer Institute
        • Hoofdonderzoeker:
          • Melissa A. Burns
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 877-442-3324
      • Worcester, Massachusetts, Verenigde Staten, 01655
        • Werving
        • UMass Memorial Medical Center - University Campus
        • Contact:
        • Hoofdonderzoeker:
          • Stefanie R. Lowas
    • Michigan
      • Ann Arbor, Michigan, Verenigde Staten, 48109
        • Werving
        • C S Mott Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-865-1125
        • Hoofdonderzoeker:
          • Joshua W. Goldman
      • Detroit, Michigan, Verenigde Staten, 48201
      • Grand Rapids, Michigan, Verenigde Staten, 49503
        • Werving
        • Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Kathleen Y. Butler
      • Kalamazoo, Michigan, Verenigde Staten, 49007
        • Werving
        • Bronson Methodist Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Kathleen Y. Butler
    • Minnesota
      • Minneapolis, Minnesota, Verenigde Staten, 55404
        • Werving
        • Children's Hospitals and Clinics of Minnesota - Minneapolis
        • Hoofdonderzoeker:
          • Michael K. Richards
        • Contact:
      • Minneapolis, Minnesota, Verenigde Staten, 55455
        • Werving
        • University of Minnesota/Masonic Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 612-624-2620
        • Hoofdonderzoeker:
          • Peter M. Gordon
      • Rochester, Minnesota, Verenigde Staten, 55905
        • Werving
        • Mayo Clinic in Rochester
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 855-776-0015
        • Hoofdonderzoeker:
          • Madeleine O'Keefe
    • Mississippi
      • Jackson, Mississippi, Verenigde Staten, 39216
        • Werving
        • University of Mississippi Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 601-815-6700
        • Hoofdonderzoeker:
          • Amanda Strobel
    • Missouri
      • Kansas City, Missouri, Verenigde Staten, 64108
        • Werving
        • Children's Mercy Hospitals and Clinics
        • Hoofdonderzoeker:
          • Keith J. August
        • Contact:
      • St Louis, Missouri, Verenigde Staten, 63110
        • Werving
        • Washington University School of Medicine
        • Contact:
        • Hoofdonderzoeker:
          • Laura G. Schuettpelz
      • St Louis, Missouri, Verenigde Staten, 63141
        • Werving
        • Mercy Hospital Saint Louis
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 314-251-7066
        • Hoofdonderzoeker:
          • Robin D. Hanson
    • Nebraska
      • Omaha, Nebraska, Verenigde Staten, 68114
        • Werving
        • Children's Hospital and Medical Center of Omaha
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 402-955-3949
        • Hoofdonderzoeker:
          • Jill C. Beck
    • Nevada
      • Las Vegas, Nevada, Verenigde Staten, 89135
        • Werving
        • Alliance for Childhood Diseases/Cure 4 the Kids Foundation
        • Contact:
        • Hoofdonderzoeker:
          • Joseph L. Lasky
    • New Hampshire
      • Lebanon, New Hampshire, Verenigde Staten, 03756
        • Werving
        • Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
        • Hoofdonderzoeker:
          • Angela Ricci
        • Contact:
    • New Jersey
      • Hackensack, New Jersey, Verenigde Staten, 07601
        • Werving
        • Hackensack University Medical Center
        • Hoofdonderzoeker:
          • Jing Chen
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 551-996-2897
      • Morristown, New Jersey, Verenigde Staten, 07960
        • Werving
        • Morristown Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 973-971-5900
        • Hoofdonderzoeker:
          • Kathryn L. Laurie
      • Neptune City, New Jersey, Verenigde Staten, 07753
        • Werving
        • Jersey Shore Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 732-776-4240
        • Hoofdonderzoeker:
          • Jing Chen
      • New Brunswick, New Jersey, Verenigde Staten, 08903
        • Werving
        • Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital
        • Hoofdonderzoeker:
          • Marissa Botwinick
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 732-235-8675
      • Paterson, New Jersey, Verenigde Staten, 07503
        • Werving
        • Saint Joseph's Regional Medical Center
        • Contact:
        • Hoofdonderzoeker:
          • Alissa Kahn
    • New Mexico
      • Albuquerque, New Mexico, Verenigde Staten, 87106
        • Werving
        • University of New Mexico Cancer Center
        • Contact:
        • Hoofdonderzoeker:
          • Jessica M. Valdez
      • Albuquerque, New Mexico, Verenigde Staten, 87106
        • Werving
        • Presbyterian Hospital
        • Hoofdonderzoeker:
          • Beeling Armijo
        • Contact:
    • New York
      • Albany, New York, Verenigde Staten, 12208
        • Werving
        • Albany Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 518-262-5513
        • Hoofdonderzoeker:
          • Lauren R. Weintraub
      • Buffalo, New York, Verenigde Staten, 14263
        • Werving
        • Roswell Park Cancer Institute
        • Contact:
        • Hoofdonderzoeker:
          • Lisa Niswander
      • Mineola, New York, Verenigde Staten, 11501
        • Werving
        • NYU Langone Hospital - Long Island
        • Contact:
        • Hoofdonderzoeker:
          • Chana L. Glasser
      • New Hyde Park, New York, Verenigde Staten, 11040
        • Werving
        • The Steven and Alexandra Cohen Children's Medical Center of New York
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 718-470-3460
        • Hoofdonderzoeker:
          • Hiren Patel
      • New York, New York, Verenigde Staten, 10032
        • Werving
        • NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
        • Hoofdonderzoeker:
          • Lewis B. Silverman
        • Contact:
      • New York, New York, Verenigde Staten, 10065
        • Werving
        • Memorial Sloan Kettering Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 212-639-7592
        • Hoofdonderzoeker:
          • Kavitha Ramaswamy
      • New York, New York, Verenigde Staten, 10016
        • Werving
        • Laura and Isaac Perlmutter Cancer Center at NYU Langone
        • Hoofdonderzoeker:
          • Elizabeth A. Raetz
        • Contact:
      • New York, New York, Verenigde Staten, 10065
        • Werving
        • NYP/Weill Cornell Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 212-746-1848
        • Hoofdonderzoeker:
          • Jaclyn Rosenzweig
      • Stony Brook, New York, Verenigde Staten, 11794
        • Werving
        • Stony Brook University Medical Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-862-2215
        • Hoofdonderzoeker:
          • Laura E. Hogan
      • Syracuse, New York, Verenigde Staten, 13210
        • Werving
        • State University of New York Upstate Medical University
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 315-464-5476
        • Hoofdonderzoeker:
          • Melanie A. Comito
      • The Bronx, New York, Verenigde Staten, 10467
        • Werving
        • Montefiore Medical Center - Moses Campus
        • Contact:
        • Hoofdonderzoeker:
          • Alice Lee
      • Valhalla, New York, Verenigde Staten, 10595
        • Werving
        • New York Medical College
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 914-594-3794
        • Hoofdonderzoeker:
          • Andrew J. Bellantoni
    • North Carolina
      • Asheville, North Carolina, Verenigde Staten, 28801
      • Chapel Hill, North Carolina, Verenigde Staten, 27599
        • Werving
        • UNC Lineberger Comprehensive Cancer Center
        • Contact:
        • Hoofdonderzoeker:
          • Thomas B. Alexander
      • Charlotte, North Carolina, Verenigde Staten, 28203
        • Werving
        • Carolinas Medical Center/Levine Cancer Institute
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-804-9376
        • Hoofdonderzoeker:
          • Joel A. Kaplan
      • Durham, North Carolina, Verenigde Staten, 27710
        • Werving
        • Duke University Medical Center
        • Hoofdonderzoeker:
          • Jessica M. Sun
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 888-275-3853
      • Winston-Salem, North Carolina, Verenigde Staten, 27157
        • Werving
        • Wake Forest University Health Sciences
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 336-713-6771
        • Hoofdonderzoeker:
          • Sarah Supples
    • North Dakota
      • Fargo, North Dakota, Verenigde Staten, 58122
    • Ohio
      • Akron, Ohio, Verenigde Staten, 44308
        • Werving
        • Children's Hospital Medical Center of Akron
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 330-543-3193
        • Hoofdonderzoeker:
          • Lauren R. Draper
      • Cincinnati, Ohio, Verenigde Staten, 45229
        • Werving
        • Cincinnati Children's Hospital Medical Center
        • Contact:
        • Hoofdonderzoeker:
          • Erin H. Breese
      • Cleveland, Ohio, Verenigde Staten, 44106
        • Werving
        • Rainbow Babies and Childrens Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 216-844-5437
        • Hoofdonderzoeker:
          • Duncan S. Stearns
      • Columbus, Ohio, Verenigde Staten, 43205
      • Dayton, Ohio, Verenigde Staten, 45404
        • Werving
        • Dayton Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-228-4055
        • Hoofdonderzoeker:
          • Jordan M. Wright
      • Toledo, Ohio, Verenigde Staten, 43606
        • Werving
        • ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Jamie L. Dargart
    • Oklahoma
      • Oklahoma City, Oklahoma, Verenigde Staten, 73104
        • Werving
        • University of Oklahoma Health Sciences Center
        • Contact:
        • Hoofdonderzoeker:
          • Rene Y. McNall-Knapp
    • Pennsylvania
      • Allentown, Pennsylvania, Verenigde Staten, 18103
        • Werving
        • Lehigh Valley Hospital-Cedar Crest
        • Contact:
        • Hoofdonderzoeker:
          • Jacob A. Troutman
      • Hershey, Pennsylvania, Verenigde Staten, 17033
        • Werving
        • Penn State Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 717-531-6012
        • Hoofdonderzoeker:
          • Lisa M. McGregor
      • Philadelphia, Pennsylvania, Verenigde Staten, 19104
        • Werving
        • Children's Hospital of Philadelphia
        • Hoofdonderzoeker:
          • Sarah K. Tasian
        • Contact:
      • Philadelphia, Pennsylvania, Verenigde Staten, 19134
        • Werving
        • Saint Christopher's Hospital for Children
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 215-427-8991
        • Hoofdonderzoeker:
          • Gregory E. Halligan
      • Pittsburgh, Pennsylvania, Verenigde Staten, 15224
        • Werving
        • Children's Hospital of Pittsburgh of UPMC
        • Contact:
        • Hoofdonderzoeker:
          • Colleen Mathews
    • Rhode Island
      • Providence, Rhode Island, Verenigde Staten, 02903
        • Werving
        • Rhode Island Hospital
        • Hoofdonderzoeker:
          • Bradley DeNardo
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 401-444-1488
    • South Carolina
      • Columbia, South Carolina, Verenigde Staten, 29203
        • Werving
        • Prisma Health Richland Hospital
        • Hoofdonderzoeker:
          • Stuart L. Cramer
        • Contact:
      • Greenville, South Carolina, Verenigde Staten, 29605
        • Werving
        • BI-LO Charities Children's Cancer Center
        • Hoofdonderzoeker:
          • Aniket Saha
        • Contact:
    • South Dakota
      • Sioux Falls, South Dakota, Verenigde Staten, 57117-5134
    • Tennessee
      • Knoxville, Tennessee, Verenigde Staten, 37916
        • Werving
        • East Tennessee Childrens Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 865-541-8266
        • Hoofdonderzoeker:
          • Susan E. Spiller
      • Nashville, Tennessee, Verenigde Staten, 37232
        • Werving
        • Vanderbilt University/Ingram Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 800-811-8480
        • Hoofdonderzoeker:
          • Brianna N. Smith
      • Nashville, Tennessee, Verenigde Staten, 37203
        • Werving
        • The Children's Hospital at TriStar Centennial
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 615-342-1919
        • Hoofdonderzoeker:
          • Clinton M. Carroll
    • Texas
      • Austin, Texas, Verenigde Staten, 78723
      • Corpus Christi, Texas, Verenigde Staten, 78411
        • Werving
        • Driscoll Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Nkechi I. Mba
      • Dallas, Texas, Verenigde Staten, 75390
        • Werving
        • UT Southwestern/Simmons Cancer Center-Dallas
        • Contact:
        • Hoofdonderzoeker:
          • Tamra L. Slone
      • Dallas, Texas, Verenigde Staten, 75230
        • Werving
        • Medical City Dallas Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 972-566-5588
        • Hoofdonderzoeker:
          • Maurizio L. Ghisoli
      • El Paso, Texas, Verenigde Staten, 79905
        • Werving
        • El Paso Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Benjamin Carcamo
      • Fort Worth, Texas, Verenigde Staten, 76104
      • Houston, Texas, Verenigde Staten, 77030
        • Werving
        • Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 713-798-1354
          • E-mail: burton@bcm.edu
        • Hoofdonderzoeker:
          • Chelsea Vrana
      • Lubbock, Texas, Verenigde Staten, 79410
        • Werving
        • Covenant Children's Hospital
        • Hoofdonderzoeker:
          • Kishor M. Bhende
        • Contact:
      • Lubbock, Texas, Verenigde Staten, 79415
        • Werving
        • UMC Cancer Center / UMC Health System
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 806-775-8590
        • Hoofdonderzoeker:
          • Erin K. Barr
      • San Antonio, Texas, Verenigde Staten, 78207
        • Werving
        • Children's Hospital of San Antonio
        • Contact:
        • Hoofdonderzoeker:
          • Julie Voeller
      • San Antonio, Texas, Verenigde Staten, 78229
        • Werving
        • University of Texas Health Science Center at San Antonio
        • Contact:
        • Hoofdonderzoeker:
          • Anne-Marie R. Langevin
      • San Antonio, Texas, Verenigde Staten, 78229
        • Werving
        • Methodist Children's Hospital of South Texas
        • Contact:
        • Hoofdonderzoeker:
          • Jose M. Esquilin
      • Temple, Texas, Verenigde Staten, 76508
        • Werving
        • Scott and White Memorial Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 254-724-5407
        • Hoofdonderzoeker:
          • Nicholas W. McGregor
    • Utah
      • Salt Lake City, Utah, Verenigde Staten, 84113
        • Werving
        • Primary Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 801-585-5270
        • Hoofdonderzoeker:
          • David S. Mangum
    • Vermont
      • Burlington, Vermont, Verenigde Staten, 05405
        • Werving
        • University of Vermont and State Agricultural College
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 802-656-8990
          • E-mail: rpo@uvm.edu
        • Hoofdonderzoeker:
          • Jessica L. Heath
    • Virginia
      • Charlottesville, Virginia, Verenigde Staten, 22908
      • Falls Church, Virginia, Verenigde Staten, 22042
        • Werving
        • Inova Fairfax Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Robin Y. Dulman
      • Norfolk, Virginia, Verenigde Staten, 23507
        • Werving
        • Children's Hospital of The King's Daughters
        • Contact:
        • Hoofdonderzoeker:
          • Melissa S. Mark
      • Richmond, Virginia, Verenigde Staten, 23298
        • Werving
        • VCU Massey Comprehensive Cancer Center
        • Hoofdonderzoeker:
          • Jordyn R. Griffin
        • Contact:
      • Roanoke, Virginia, Verenigde Staten, 24014
        • Werving
        • Carilion Children's
        • Contact:
        • Hoofdonderzoeker:
          • Erwood G. Edwards
    • Washington
      • Seattle, Washington, Verenigde Staten, 98105
        • Werving
        • Seattle Children's Hospital
        • Contact:
          • Site Public Contact
          • Telefoonnummer: 866-987-2000
        • Hoofdonderzoeker:
          • Sarah E. Leary
      • Spokane, Washington, Verenigde Staten, 99204
        • Werving
        • Providence Sacred Heart Medical Center and Children's Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Judy L. Felgenhauer
      • Tacoma, Washington, Verenigde Staten, 98405
        • Werving
        • Mary Bridge Children's Hospital and Health Center
        • Contact:
        • Hoofdonderzoeker:
          • Robert G. Irwin
    • Wisconsin
      • Green Bay, Wisconsin, Verenigde Staten, 54301
        • Werving
        • Saint Vincent Hospital Cancer Center Green Bay
        • Hoofdonderzoeker:
          • Catherine A. Long
        • Contact:
      • Madison, Wisconsin, Verenigde Staten, 53792
        • Werving
        • University of Wisconsin Carbone Cancer Center - University Hospital
        • Contact:
        • Hoofdonderzoeker:
          • Cathy A. Lee-Miller
      • Milwaukee, Wisconsin, Verenigde Staten, 53226
        • Werving
        • Children's Hospital of Wisconsin
        • Contact:
        • Hoofdonderzoeker:
          • Paul D. Harker-Murray

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

1 jaar tot 46 jaar (Kind, Volwassen)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Patients must be > 365 days and < 18 years (for AIEOP-BFM), > 365 days and < 22 years (for Children's Oncology Group [COG]) and > 365 days and < 46 years (for ALLTogether sites) at the time of enrollment

  • Newly-diagnosed Ph+ or ABL-class Ph-like B-ALL. Leukemic blasts must express CD19. ABL-class fusions are defined as rearrangements involving the following genes predicted to be sensitive to imatinib and/or dasatinib: ABL1, ABL2, CSF1R, and PDGFRB

  • Evidence of BCR::ABL1 should be documented by a clinically-validated assay prior to study entry on day 15 from the first dose of vinCRIStine during Induction therapy. ABL-class Ph-like B-ALL gene rearrangements should be documented by a clinically-validated assay and enrolled on study by day 1 of Blinatumomab Block 1. Accepted methods of detection include fluorescence in situ hybridization (FISH) using break-apart of colocalization signal probes, singleplex or multiplex reverse-transcription polymerase chain reaction (RT-PCR), whole-transcriptome or panel-based ribonucleic acid (RNA) sequencing (e.g., Hematologic Cancer Fusion Analysis, TruSight RNA Pan-Cancer Panel or equivalent). Confirmation of 5' fusion partner genes is not required for study enrollment

  • Patients with Ph+ B-ALL must have previously started Induction therapy, which includes vinCRIStine, a corticosteroid, pegaspargase or calaspargase pegol, with or without anthracycline, and/or other standard cytotoxic chemotherapy

  • Patients with Ph+ B-ALL have not received more than 14 days of systemic Induction therapy beginning with the first Induction dose of vinCRIStine

  • Patients with ABL-class Ph-like B-ALL must have previously completed 4 or 5 weeks of multiagent Induction chemotherapy (Induction 1A)

  • Patients may have started either imatinib or dasatinib prior to study entry but should have received no more than 14 days of TKI for Ph+ B-ALL or no more than 35 days of TKI for ABL-class Ph-like B-ALL

  • Patients must have a performance status corresponding to Eastern Cooperative Oncology Group (ECOG) scores of ≤ 2 or Karnofsky and Lansky performance scores ≥ 50%. Use Karnofsky for patients > 16 years of age and Lansky for patients ≤ 16 years of age

  • For pediatric patients (age 1-17 years): a glomerular filtration rate (GFR) ≥ 50 mL/min/1.73 m^2, as determined by one of the following methods (must be performed within 7 days prior to enrollment unless otherwise indicated):

    • Estimated GFR (eGFR) ≥ 50 mL/min/1.73 m2
    • Measured GFR ≥ 50 mL/min/1.73 m^2 (any age). If measured GFR is used, it must be performed using direct measurement with a nuclear blood sampling method or small molecule clearance method (iothalamate or other molecule per institutional standard

  • For adult patients (age 18 years or older): Creatinine clearance ≥ 30 mL/min, as estimated by the Cockcroft and Gault formula. The creatinine value used in the calculation must have been obtained within 28 days prior to registration. Estimated creatinine clearance is based on body weight

  • Direct bilirubin < 2.0 mg/dL (34.2 micromoles/L) (must be performed within 7 days prior to enrollment unless otherwise indicated)

  • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 10 x upper limit of normal (ULN) (must be performed within 7 days prior to enrollment unless otherwise indicated)

  • * Shortening fraction of ≥ 27% by echocardiogram (must be obtained within 21 days prior to enrollment and start of protocol therapy [repeat if necessary]) OR

    • Left Ventricular Ejection fraction of ≥ 50% by radionuclide angiogram or echocardiogram (must be obtained within 21 days prior to enrollment and start of protocol therapy [repeat if necessary]) AND

    • Corrected QT Interval, QTc < 480mSec (must be obtained within 21 days prior to enrollment and start of protocol therapy [repeat if necessary])

      • Note: Repeat echocardiogram and electrocardiogram are not required if they were performed at or after initial ALL diagnosis before study enrollment

Exclusion Criteria:

  • Known history of chronic myeloid leukemia (CML)

  • ABL-class Ph-like B-ALL who are CNS2 or CNS3 at end of Induction phase

  • ALL developing after a previous cancer treated with cytotoxic chemotherapy

  • Active, uncontrolled infection or active systemic illness that requires ongoing vasopressor support or mechanical ventilation

  • Down syndrome (trisomy 21)

  • Pregnancy and breast feeding

    • Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A negative pregnancy test is required for female patients of childbearing potential within 7 days prior to enrollment

    • Lactating females who plan to breastfeed their infants

    • Sexually active male and female patients of reproductive potential who have not agreed to use an effective contraception method for the duration of treatment according to protocol

      • NOTE: Patients who could become pregnant or could father a child must use effective contraception during protocol treatment and for 30 days after the last dose of dasatinib or 14 days after the last dose of imatinib dose or per institutional standard of care for multiagent chemotherapy, whichever is longer

  • Prior treatment with TKIs before study entry with the exception of imatinib or dasatinib

  • Patients with congenital long QT syndrome, history of ventricular arrhythmias, or heart block

  • Patients with known Charcot-Marie-Tooth disease

  • Patients with significant central nervous system pathology that would preclude treatment with blinatumomab, including history of severe neurologic disorder or autoimmune disease with central nervous system (CNS) involvement

    • Note: Patients with a history of seizures that are well controlled on stable doses of anti-epileptic drugs are eligible. Patients with a history of cerebrovascular ischemia/hemorrhage with residual deficits are not eligible. Patients with a history of cerebrovascular ischemia/hemorrhage remain eligible provided all neurologic deficits have resolved

  • HIV-infected patients are eligible if on effective anti-retroviral therapy that does not interact with planned study agents and with undetectable viral load within 6 months of treatment

  • All patients and/or their parents or legal guardians must sign a written informed consent

  • All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Niet-gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Stratum I (Ph+ ALL)

See detailed description
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andere namen:
  • Biopsie van beenmerg
  • Biopsie, beenmerg
Procedure: Echocardiography Test

Undergo ECHO

Andere namen:
  • Echocardiografie
  • EG
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andere namen:
  • Blood Pool-scan
  • Equilibrium radionuclide angiografie
  • Gated Blood Pool-beeldvorming
  • MUGA
  • Radionuclide ventriculografie
  • RNVG
  • SYMA scannen
  • Gesynchroniseerde Multigated Acquisitie Scannen
  • MUGA-scan
  • Multi-Gated Acquisitie Scan
  • Radionuclide ventriculogram scan
  • Gated Heart Pool-scan
  • RNV-scan
Procedure: Biospecimen Collection

Undergo blood and CSF sample collection

Andere namen:
  • Biologische monsterverzameling
  • Biospecimen verzameld
  • Specimenverzameling
  • Monsterverzameling
Biologisch: Blinatumomab

Receive IV

Andere namen:
  • Blincyto
  • Anti-CD19 x Anti-CD3 bispecifiek monoklonaal antilichaam
  • Anti-CD19/Anti-CD3 recombinant bispecifiek monoklonaal antilichaam MT103
  • MEDI-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
Geneesmiddel: Calaspargase Pegol

Receive IV

Andere namen:
  • Asparaginase (Escherichia coli Iso-enzym II), conjugaat met alfa-(((2,5-dioxo-1-pyrrolidinyl)oxy)carbonyl)-omega-methoxypoly(oxy-1,2-ethaandiyl)
  • Asparlas
  • EZN-2285
  • SC-PEG E. Coli L-asparaginase
  • Succinimidylcarbonaat monomethoxypolyethyleenglycol E. coli L-asparaginase
  • Calaspargase Pegol-mknl
Geneesmiddel: Cyclophosphamide

Receive IV

Andere namen:
  • Cytoxaan
  • CTX
  • (-)-cyclofosfamide
  • 2H-1,3,2-Oxazafosforine, 2-[bis(2-chloorethyl)amino]tetrahydro-, 2-oxide, monohydraat
  • Carloxan
  • Ciclofosfamida
  • Ciclofosfamide
  • Cicloxal
  • Clafen
  • Clafeen
  • CP monohydraat
  • CYCLO-cel
  • Cycloblastine
  • Cyclofosfam
  • Cyclofosfamide-monohydraat
  • Cyclofosfamidum
  • Cyclofosfan
  • Cyclofosfaan
  • Cyclofosfanum
  • Cyclostine
  • Cytofosfan
  • Cytofosfaan
  • Fosfaseron
  • Genoxal
  • Genuxaal
  • Ledoxine
  • Mitoxan
  • Neosar
  • Opwekken
  • Syklofosfamide
  • WR-138719
  • Asta B 518
  • B-518
  • B518
  • WR138719
  • Frindovyx
Geneesmiddel: Cytarabine

Receive IV or subcutaneously

Andere namen:
  • Β-Cytosine arabinoside
  • 1-ß-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-P-D-Arabinofuranosylcytosine
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosine
  • 1.beta.-D-Arabinofuranosylcytosine
  • 2(1H)-pyrimidinon, 4-amino-1-bèta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1β-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-cel
  • Arabier
  • Arabinofuranosylcytosine
  • Arabinosylcytosine
  • Aracytidine
  • Aracytine
  • Beta-Cytosine Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosine arabinoside
  • Cytosine-β-arabinoside
  • Cytosine-bèta-arabinoside
  • Erpalfa
  • Starasid
  • Tarabine PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Geneesmiddel: Dasatinib

Receive PO

Andere namen:
  • BMS-354825
  • Dasatinib hydraat
  • Dasatinib-monohydraat
  • Sprycel
  • GBS 354825
  • BMS354825
Geneesmiddel: Daunorubicin

Receive IV

Andere namen:
  • DNR
  • Rubidomycine
  • Daunomycine
  • Daunorrubicina
  • Leukaemomycine C
  • Rubomycine C
Geneesmiddel: Doxorubicin

Receive IV

Andere namen:
  • Adriablastine
  • Hydroxydaunomycine
  • Hydroxyl Daunorubicine
  • Hydroxyldaunorubicine
Geneesmiddel: Leucovorin

Receive PO or IV

Andere namen:
  • Folinezuur
Geneesmiddel: Mercaptopurine

Receive PO

Andere namen:
  • 6 MP
  • Purinethol
  • 3H-purine-6-thiol
  • 6 Thiohypoxanthine
  • 6 Thiopurine
  • 6-mercaptopurine
  • 6-Mercaptopurine-monohydraat
  • 6-Purinethiol
  • 6-thiopurine
  • 6-Thioxopurine
  • 6H-Purine-6-thion, 1,7-dihydro- (9CI)
  • 7-Mercapto-1,3,4,6-tetrazaïndeen
  • Alti-Mercaptopurine
  • Azathiopurine
  • Bw 57-323H
  • Flocofil
  • Ismipur
  • Leukerin
  • Leupurine
  • Mercaleukim
  • Mercaleukin
  • Mercaptina
  • Mercaptopurinum
  • Mercapurine
  • Merens
  • NCI-C04886
  • Puri-Nethol
  • Purimethol
  • Purine, 6-mercapto-
  • Purine-6-thiol (8CI)
  • Purine-6-thiol, monohydraat
  • Purinethiol
  • U-4748
  • WR-2785
Geneesmiddel: Methotrexate

Receive IT or IV or PO

Andere namen:
  • Abitrexaat
  • Folex
  • Mexaat
  • MTX
  • Alfa-Methopterine
  • Amethopterine
  • Brimexaat
  • KL 14377
  • CL-14377
  • Emtexeren
  • Emtexaat
  • Emthexaat
  • Farmitrexaat
  • Fauldexato
  • Folex PFS
  • Lantarel
  • Ledertrexaat
  • Lumexon
  • Maxtrex
  • Medsatrexaat
  • Metex
  • Methoblastine
  • Methotrexaat LPF
  • Methotrexaat Methylaminopterine
  • Methotrexatum
  • Metotrexato
  • Metrotex
  • Mexaat-AQ
  • Novatrex
  • Reumatrex
  • Texaat
  • Tremetex
  • Trexeron
  • Trixilem
  • WR-19039
  • Jylamvo
Geneesmiddel: Pegaspargase

Receive IV or intramuscularly

Andere namen:
  • L-asparaginase met polyethyleenglycol
  • Oncaspar
  • Oncaspar-IV
  • PEG-asparaginase
  • PEG-L-asparaginase
  • PEG-L-asparaginase (Enzon - Kyowa Hakko)
  • PEGLA
  • Polyethyleenglycol L-asparaginase
  • Polyethyleen Glycol-L-Asparaginase
Geneesmiddel: Prednisolone

Receive PO

Andere namen:
  • (11beta)-11,17,21-Trihydroxypregna-1,4-dieen-3,20-dion
  • .delta.1-Hydrocortison
  • Adnisolon
  • Aprednislon
  • Capsoïde
  • Cortalon
  • Cortisolon
  • Dacortin H
  • Decaprednil
  • Decortin H
  • Delta(1)Hydrocortison
  • Delta Cortef
  • Delta-Diona
  • Delta-F
  • Delta-Phoricol
  • Delta1-dehydro-hydrocortison
  • Deltacortril
  • Deltahydrocortison
  • Deltasolone
  • Deltasol
  • Dhasolone
  • Di-Adreson-F
  • Dontisolon D
  • Estilson
  • Fisopred
  • Frisolona
  • Gupisone
  • Hostacortine H
  • Hydeltra
  • Hydeltrasol
  • Klimmacort
  • Kuhlprednon
  • Lenisolon
  • Lepi-Cortinolo
  • Linola-H N
  • Linola-H-Fett N
  • Longiprednil
  • Metacortandralon
  • Meti Derm
  • Meticortelon
  • Opredson
  • Panafcortelon
  • Precortisyl
  • Pred-Clysma
  • Predeltilon
  • Predni-Coelin
  • Predni-Helvacort
  • Prednicortelon
  • Prednisolon
  • Prelone
  • Prenilon
  • Steraan
Geneesmiddel: Prednisone

Receive PO

Andere namen:
  • Deltason
  • Orason
  • .delta.1-cortisone
  • 1, 2-dehydrocortison
  • Adason
  • Cortantyl
  • Dacortin
  • DeCortin
  • Decortyl
  • Decorton
  • Delta 1-cortisone
  • Delta-koepel
  • Deltacorteen
  • Deltacortison
  • Deltadehydrocortison
  • Deltison
  • Delta
  • Econosone
  • Lisacort
  • Meprosona-F
  • Metacortandracine
  • Meticorten
  • Ofisolona
  • Panafcort
  • Panasol-S
  • Paracort
  • Perrigo Prednison
  • PRED
  • Voorspeller
  • Voorspellen
  • Prednicen-M
  • Prednicort
  • Prednidib
  • Prednilonga
  • Predniment
  • Prednison Intensol
  • Prednison
  • Predniton
  • Promifen
  • Rayo's
  • Servies
  • SK-Prednison
Geneesmiddel: Vincristine

Receive IV

Andere namen:
  • Videorecorder
  • Leurocristine
  • Vincristine
  • LCR
Experimenteel: Stratum II (PDGFRB ABL-Class fusions)

See detailed description.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andere namen:
  • Biopsie van beenmerg
  • Biopsie, beenmerg
Procedure: Echocardiography Test

Undergo ECHO

Andere namen:
  • Echocardiografie
  • EG
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andere namen:
  • Blood Pool-scan
  • Equilibrium radionuclide angiografie
  • Gated Blood Pool-beeldvorming
  • MUGA
  • Radionuclide ventriculografie
  • RNVG
  • SYMA scannen
  • Gesynchroniseerde Multigated Acquisitie Scannen
  • MUGA-scan
  • Multi-Gated Acquisitie Scan
  • Radionuclide ventriculogram scan
  • Gated Heart Pool-scan
  • RNV-scan
Straling: Radiation Therapy

Undergo radiation therapy

Andere namen:
  • Radiotherapie bij kanker
  • ENERGY_TYPE
  • Bestralen
  • Bestraald
  • Bestraling
  • Straling
  • Radiotherapie, NOS
  • Radiotherapie
  • RT
  • Therapie, bestraling
  • Energie Type
Procedure: Biospecimen Collection

Undergo blood and CSF sample collection

Andere namen:
  • Biologische monsterverzameling
  • Biospecimen verzameld
  • Specimenverzameling
  • Monsterverzameling
Biologisch: Blinatumomab

Receive IV

Andere namen:
  • Blincyto
  • Anti-CD19 x Anti-CD3 bispecifiek monoklonaal antilichaam
  • Anti-CD19/Anti-CD3 recombinant bispecifiek monoklonaal antilichaam MT103
  • MEDI-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
Geneesmiddel: Calaspargase Pegol

Receive IV

Andere namen:
  • Asparaginase (Escherichia coli Iso-enzym II), conjugaat met alfa-(((2,5-dioxo-1-pyrrolidinyl)oxy)carbonyl)-omega-methoxypoly(oxy-1,2-ethaandiyl)
  • Asparlas
  • EZN-2285
  • SC-PEG E. Coli L-asparaginase
  • Succinimidylcarbonaat monomethoxypolyethyleenglycol E. coli L-asparaginase
  • Calaspargase Pegol-mknl
Geneesmiddel: Cyclophosphamide

Receive IV

Andere namen:
  • Cytoxaan
  • CTX
  • (-)-cyclofosfamide
  • 2H-1,3,2-Oxazafosforine, 2-[bis(2-chloorethyl)amino]tetrahydro-, 2-oxide, monohydraat
  • Carloxan
  • Ciclofosfamida
  • Ciclofosfamide
  • Cicloxal
  • Clafen
  • Clafeen
  • CP monohydraat
  • CYCLO-cel
  • Cycloblastine
  • Cyclofosfam
  • Cyclofosfamide-monohydraat
  • Cyclofosfamidum
  • Cyclofosfan
  • Cyclofosfaan
  • Cyclofosfanum
  • Cyclostine
  • Cytofosfan
  • Cytofosfaan
  • Fosfaseron
  • Genoxal
  • Genuxaal
  • Ledoxine
  • Mitoxan
  • Neosar
  • Opwekken
  • Syklofosfamide
  • WR-138719
  • Asta B 518
  • B-518
  • B518
  • WR138719
  • Frindovyx
Geneesmiddel: Cytarabine

Receive IV or subcutaneously

Andere namen:
  • Β-Cytosine arabinoside
  • 1-ß-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-P-D-Arabinofuranosylcytosine
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosine
  • 1.beta.-D-Arabinofuranosylcytosine
  • 2(1H)-pyrimidinon, 4-amino-1-bèta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1β-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-cel
  • Arabier
  • Arabinofuranosylcytosine
  • Arabinosylcytosine
  • Aracytidine
  • Aracytine
  • Beta-Cytosine Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosine arabinoside
  • Cytosine-β-arabinoside
  • Cytosine-bèta-arabinoside
  • Erpalfa
  • Starasid
  • Tarabine PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Geneesmiddel: Daunorubicin

Receive IV

Andere namen:
  • DNR
  • Rubidomycine
  • Daunomycine
  • Daunorrubicina
  • Leukaemomycine C
  • Rubomycine C
Geneesmiddel: Doxorubicin

Receive IV

Andere namen:
  • Adriablastine
  • Hydroxydaunomycine
  • Hydroxyl Daunorubicine
  • Hydroxyldaunorubicine
Geneesmiddel: Leucovorin

Receive PO or IV

Andere namen:
  • Folinezuur
Geneesmiddel: Mercaptopurine

Receive PO

Andere namen:
  • 6 MP
  • Purinethol
  • 3H-purine-6-thiol
  • 6 Thiohypoxanthine
  • 6 Thiopurine
  • 6-mercaptopurine
  • 6-Mercaptopurine-monohydraat
  • 6-Purinethiol
  • 6-thiopurine
  • 6-Thioxopurine
  • 6H-Purine-6-thion, 1,7-dihydro- (9CI)
  • 7-Mercapto-1,3,4,6-tetrazaïndeen
  • Alti-Mercaptopurine
  • Azathiopurine
  • Bw 57-323H
  • Flocofil
  • Ismipur
  • Leukerin
  • Leupurine
  • Mercaleukim
  • Mercaleukin
  • Mercaptina
  • Mercaptopurinum
  • Mercapurine
  • Merens
  • NCI-C04886
  • Puri-Nethol
  • Purimethol
  • Purine, 6-mercapto-
  • Purine-6-thiol (8CI)
  • Purine-6-thiol, monohydraat
  • Purinethiol
  • U-4748
  • WR-2785
Geneesmiddel: Methotrexate

Receive IT or IV or PO

Andere namen:
  • Abitrexaat
  • Folex
  • Mexaat
  • MTX
  • Alfa-Methopterine
  • Amethopterine
  • Brimexaat
  • KL 14377
  • CL-14377
  • Emtexeren
  • Emtexaat
  • Emthexaat
  • Farmitrexaat
  • Fauldexato
  • Folex PFS
  • Lantarel
  • Ledertrexaat
  • Lumexon
  • Maxtrex
  • Medsatrexaat
  • Metex
  • Methoblastine
  • Methotrexaat LPF
  • Methotrexaat Methylaminopterine
  • Methotrexatum
  • Metotrexato
  • Metrotex
  • Mexaat-AQ
  • Novatrex
  • Reumatrex
  • Texaat
  • Tremetex
  • Trexeron
  • Trixilem
  • WR-19039
  • Jylamvo
Geneesmiddel: Pegaspargase

Receive IV or intramuscularly

Andere namen:
  • L-asparaginase met polyethyleenglycol
  • Oncaspar
  • Oncaspar-IV
  • PEG-asparaginase
  • PEG-L-asparaginase
  • PEG-L-asparaginase (Enzon - Kyowa Hakko)
  • PEGLA
  • Polyethyleenglycol L-asparaginase
  • Polyethyleen Glycol-L-Asparaginase
Geneesmiddel: Prednisolone

Receive PO

Andere namen:
  • (11beta)-11,17,21-Trihydroxypregna-1,4-dieen-3,20-dion
  • .delta.1-Hydrocortison
  • Adnisolon
  • Aprednislon
  • Capsoïde
  • Cortalon
  • Cortisolon
  • Dacortin H
  • Decaprednil
  • Decortin H
  • Delta(1)Hydrocortison
  • Delta Cortef
  • Delta-Diona
  • Delta-F
  • Delta-Phoricol
  • Delta1-dehydro-hydrocortison
  • Deltacortril
  • Deltahydrocortison
  • Deltasolone
  • Deltasol
  • Dhasolone
  • Di-Adreson-F
  • Dontisolon D
  • Estilson
  • Fisopred
  • Frisolona
  • Gupisone
  • Hostacortine H
  • Hydeltra
  • Hydeltrasol
  • Klimmacort
  • Kuhlprednon
  • Lenisolon
  • Lepi-Cortinolo
  • Linola-H N
  • Linola-H-Fett N
  • Longiprednil
  • Metacortandralon
  • Meti Derm
  • Meticortelon
  • Opredson
  • Panafcortelon
  • Precortisyl
  • Pred-Clysma
  • Predeltilon
  • Predni-Coelin
  • Predni-Helvacort
  • Prednicortelon
  • Prednisolon
  • Prelone
  • Prenilon
  • Steraan
Geneesmiddel: Prednisone

Receive PO

Andere namen:
  • Deltason
  • Orason
  • .delta.1-cortisone
  • 1, 2-dehydrocortison
  • Adason
  • Cortantyl
  • Dacortin
  • DeCortin
  • Decortyl
  • Decorton
  • Delta 1-cortisone
  • Delta-koepel
  • Deltacorteen
  • Deltacortison
  • Deltadehydrocortison
  • Deltison
  • Delta
  • Econosone
  • Lisacort
  • Meprosona-F
  • Metacortandracine
  • Meticorten
  • Ofisolona
  • Panafcort
  • Panasol-S
  • Paracort
  • Perrigo Prednison
  • PRED
  • Voorspeller
  • Voorspellen
  • Prednicen-M
  • Prednicort
  • Prednidib
  • Prednilonga
  • Predniment
  • Prednison Intensol
  • Prednison
  • Predniton
  • Promifen
  • Rayo's
  • Servies
  • SK-Prednison
Geneesmiddel: Vincristine

Receive IV

Andere namen:
  • Videorecorder
  • Leurocristine
  • Vincristine
  • LCR
Geneesmiddel: Imatinib

Given PO

Geneesmiddel: Thioguanine

Receive PO

Andere namen:
  • 6-TG
  • 2-Amino 6MP
  • 2-Amino-1,7-dihydro-6H-purine-6-thion
  • 2-Amino-6-mercaptopurine
  • 2-Amino-6-purinethiol
  • 2-aminopurine-6-thiol
  • 2-Aminopurine-6(1H)-thion
  • 2-Aminopurine-6-thiol
  • 2-Aminopurine-6-thiol hemihydraat
  • 2-Mercapto-6-aminopurine
  • 6-Amino-2-mercaptopurine
  • 6-Mercapto-2-aminopurine
  • 6-Mercaptoguanine
  • 6H-Purine-6-thion, 2-amino-1,7-dihydro- (9CI)
  • BW 5071
  • Lanvis
  • Tabloid
  • Thioguanine hemihydraat
  • Thioguanine hydraat
  • Tioguanin
  • Tioguanine
  • Welkom U3B
  • WR-1141
  • X 27
Experimenteel: Stratum III (non-PDGFRB ABL-Class fusions)

See detailed description.
Procedure: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andere namen:
  • Biopsie van beenmerg
  • Biopsie, beenmerg
Procedure: Echocardiography Test

Undergo ECHO

Andere namen:
  • Echocardiografie
  • EG
Procedure: Multigated Acquisition Scan

Undergo MUGA

Andere namen:
  • Blood Pool-scan
  • Equilibrium radionuclide angiografie
  • Gated Blood Pool-beeldvorming
  • MUGA
  • Radionuclide ventriculografie
  • RNVG
  • SYMA scannen
  • Gesynchroniseerde Multigated Acquisitie Scannen
  • MUGA-scan
  • Multi-Gated Acquisitie Scan
  • Radionuclide ventriculogram scan
  • Gated Heart Pool-scan
  • RNV-scan
Straling: Radiation Therapy

Undergo radiation therapy

Andere namen:
  • Radiotherapie bij kanker
  • ENERGY_TYPE
  • Bestralen
  • Bestraald
  • Bestraling
  • Straling
  • Radiotherapie, NOS
  • Radiotherapie
  • RT
  • Therapie, bestraling
  • Energie Type
Procedure: Biospecimen Collection

Undergo blood and CSF sample collection

Andere namen:
  • Biologische monsterverzameling
  • Biospecimen verzameld
  • Specimenverzameling
  • Monsterverzameling
Biologisch: Blinatumomab

Receive IV

Andere namen:
  • Blincyto
  • Anti-CD19 x Anti-CD3 bispecifiek monoklonaal antilichaam
  • Anti-CD19/Anti-CD3 recombinant bispecifiek monoklonaal antilichaam MT103
  • MEDI-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
Geneesmiddel: Calaspargase Pegol

Receive IV

Andere namen:
  • Asparaginase (Escherichia coli Iso-enzym II), conjugaat met alfa-(((2,5-dioxo-1-pyrrolidinyl)oxy)carbonyl)-omega-methoxypoly(oxy-1,2-ethaandiyl)
  • Asparlas
  • EZN-2285
  • SC-PEG E. Coli L-asparaginase
  • Succinimidylcarbonaat monomethoxypolyethyleenglycol E. coli L-asparaginase
  • Calaspargase Pegol-mknl
Geneesmiddel: Cyclophosphamide

Receive IV

Andere namen:
  • Cytoxaan
  • CTX
  • (-)-cyclofosfamide
  • 2H-1,3,2-Oxazafosforine, 2-[bis(2-chloorethyl)amino]tetrahydro-, 2-oxide, monohydraat
  • Carloxan
  • Ciclofosfamida
  • Ciclofosfamide
  • Cicloxal
  • Clafen
  • Clafeen
  • CP monohydraat
  • CYCLO-cel
  • Cycloblastine
  • Cyclofosfam
  • Cyclofosfamide-monohydraat
  • Cyclofosfamidum
  • Cyclofosfan
  • Cyclofosfaan
  • Cyclofosfanum
  • Cyclostine
  • Cytofosfan
  • Cytofosfaan
  • Fosfaseron
  • Genoxal
  • Genuxaal
  • Ledoxine
  • Mitoxan
  • Neosar
  • Opwekken
  • Syklofosfamide
  • WR-138719
  • Asta B 518
  • B-518
  • B518
  • WR138719
  • Frindovyx
Geneesmiddel: Cytarabine

Receive IV or subcutaneously

Andere namen:
  • Β-Cytosine arabinoside
  • 1-ß-D-Arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-P-D-Arabinofuranosylcytosine
  • 1-Beta-D-arabinofuranosyl-4-amino-2(1H)pyrimidinon
  • 1-Beta-D-arabinofuranosylcytosine
  • 1.beta.-D-Arabinofuranosylcytosine
  • 2(1H)-pyrimidinon, 4-amino-1-bèta-D-arabinofuranosyl-
  • 2(1H)-pyrimidinon, 4-amino-1β-D-arabinofuranosyl-
  • Alexan
  • Ara-C
  • ARA-cel
  • Arabier
  • Arabinofuranosylcytosine
  • Arabinosylcytosine
  • Aracytidine
  • Aracytine
  • Beta-Cytosine Arabinoside
  • CHX-3311
  • Cytarabinum
  • Cytarbel
  • Cytosar
  • Cytosine arabinoside
  • Cytosine-β-arabinoside
  • Cytosine-bèta-arabinoside
  • Erpalfa
  • Starasid
  • Tarabine PFS
  • U 19920
  • U-19920
  • Udicil
  • WR-28453
Geneesmiddel: Dasatinib

Receive PO

Andere namen:
  • BMS-354825
  • Dasatinib hydraat
  • Dasatinib-monohydraat
  • Sprycel
  • GBS 354825
  • BMS354825
Geneesmiddel: Daunorubicin

Receive IV

Andere namen:
  • DNR
  • Rubidomycine
  • Daunomycine
  • Daunorrubicina
  • Leukaemomycine C
  • Rubomycine C
Geneesmiddel: Doxorubicin

Receive IV

Andere namen:
  • Adriablastine
  • Hydroxydaunomycine
  • Hydroxyl Daunorubicine
  • Hydroxyldaunorubicine
Geneesmiddel: Leucovorin

Receive PO or IV

Andere namen:
  • Folinezuur
Geneesmiddel: Mercaptopurine

Receive PO

Andere namen:
  • 6 MP
  • Purinethol
  • 3H-purine-6-thiol
  • 6 Thiohypoxanthine
  • 6 Thiopurine
  • 6-mercaptopurine
  • 6-Mercaptopurine-monohydraat
  • 6-Purinethiol
  • 6-thiopurine
  • 6-Thioxopurine
  • 6H-Purine-6-thion, 1,7-dihydro- (9CI)
  • 7-Mercapto-1,3,4,6-tetrazaïndeen
  • Alti-Mercaptopurine
  • Azathiopurine
  • Bw 57-323H
  • Flocofil
  • Ismipur
  • Leukerin
  • Leupurine
  • Mercaleukim
  • Mercaleukin
  • Mercaptina
  • Mercaptopurinum
  • Mercapurine
  • Merens
  • NCI-C04886
  • Puri-Nethol
  • Purimethol
  • Purine, 6-mercapto-
  • Purine-6-thiol (8CI)
  • Purine-6-thiol, monohydraat
  • Purinethiol
  • U-4748
  • WR-2785
Geneesmiddel: Methotrexate

Receive IT or IV or PO

Andere namen:
  • Abitrexaat
  • Folex
  • Mexaat
  • MTX
  • Alfa-Methopterine
  • Amethopterine
  • Brimexaat
  • KL 14377
  • CL-14377
  • Emtexeren
  • Emtexaat
  • Emthexaat
  • Farmitrexaat
  • Fauldexato
  • Folex PFS
  • Lantarel
  • Ledertrexaat
  • Lumexon
  • Maxtrex
  • Medsatrexaat
  • Metex
  • Methoblastine
  • Methotrexaat LPF
  • Methotrexaat Methylaminopterine
  • Methotrexatum
  • Metotrexato
  • Metrotex
  • Mexaat-AQ
  • Novatrex
  • Reumatrex
  • Texaat
  • Tremetex
  • Trexeron
  • Trixilem
  • WR-19039
  • Jylamvo
Geneesmiddel: Pegaspargase

Receive IV or intramuscularly

Andere namen:
  • L-asparaginase met polyethyleenglycol
  • Oncaspar
  • Oncaspar-IV
  • PEG-asparaginase
  • PEG-L-asparaginase
  • PEG-L-asparaginase (Enzon - Kyowa Hakko)
  • PEGLA
  • Polyethyleenglycol L-asparaginase
  • Polyethyleen Glycol-L-Asparaginase
Geneesmiddel: Prednisolone

Receive PO

Andere namen:
  • (11beta)-11,17,21-Trihydroxypregna-1,4-dieen-3,20-dion
  • .delta.1-Hydrocortison
  • Adnisolon
  • Aprednislon
  • Capsoïde
  • Cortalon
  • Cortisolon
  • Dacortin H
  • Decaprednil
  • Decortin H
  • Delta(1)Hydrocortison
  • Delta Cortef
  • Delta-Diona
  • Delta-F
  • Delta-Phoricol
  • Delta1-dehydro-hydrocortison
  • Deltacortril
  • Deltahydrocortison
  • Deltasolone
  • Deltasol
  • Dhasolone
  • Di-Adreson-F
  • Dontisolon D
  • Estilson
  • Fisopred
  • Frisolona
  • Gupisone
  • Hostacortine H
  • Hydeltra
  • Hydeltrasol
  • Klimmacort
  • Kuhlprednon
  • Lenisolon
  • Lepi-Cortinolo
  • Linola-H N
  • Linola-H-Fett N
  • Longiprednil
  • Metacortandralon
  • Meti Derm
  • Meticortelon
  • Opredson
  • Panafcortelon
  • Precortisyl
  • Pred-Clysma
  • Predeltilon
  • Predni-Coelin
  • Predni-Helvacort
  • Prednicortelon
  • Prednisolon
  • Prelone
  • Prenilon
  • Steraan
Geneesmiddel: Prednisone

Receive PO

Andere namen:
  • Deltason
  • Orason
  • .delta.1-cortisone
  • 1, 2-dehydrocortison
  • Adason
  • Cortantyl
  • Dacortin
  • DeCortin
  • Decortyl
  • Decorton
  • Delta 1-cortisone
  • Delta-koepel
  • Deltacorteen
  • Deltacortison
  • Deltadehydrocortison
  • Deltison
  • Delta
  • Econosone
  • Lisacort
  • Meprosona-F
  • Metacortandracine
  • Meticorten
  • Ofisolona
  • Panafcort
  • Panasol-S
  • Paracort
  • Perrigo Prednison
  • PRED
  • Voorspeller
  • Voorspellen
  • Prednicen-M
  • Prednicort
  • Prednidib
  • Prednilonga
  • Predniment
  • Prednison Intensol
  • Prednison
  • Predniton
  • Promifen
  • Rayo's
  • Servies
  • SK-Prednison
Geneesmiddel: Vincristine

Receive IV

Andere namen:
  • Videorecorder
  • Leurocristine
  • Vincristine
  • LCR
Geneesmiddel: Thioguanine

Receive PO

Andere namen:
  • 6-TG
  • 2-Amino 6MP
  • 2-Amino-1,7-dihydro-6H-purine-6-thion
  • 2-Amino-6-mercaptopurine
  • 2-Amino-6-purinethiol
  • 2-aminopurine-6-thiol
  • 2-Aminopurine-6(1H)-thion
  • 2-Aminopurine-6-thiol
  • 2-Aminopurine-6-thiol hemihydraat
  • 2-Mercapto-6-aminopurine
  • 6-Amino-2-mercaptopurine
  • 6-Mercapto-2-aminopurine
  • 6-Mercaptoguanine
  • 6H-Purine-6-thion, 2-amino-1,7-dihydro- (9CI)
  • BW 5071
  • Lanvis
  • Tabloid
  • Thioguanine hemihydraat
  • Thioguanine hydraat
  • Tioguanin
  • Tioguanine
  • Welkom U3B
  • WR-1141
  • X 27

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Philadelphia chromosome-positive (Ph+) (BCR::ABL1-rearranged) 3-year event free survival (EFS)
Tijdsspanne: Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years

Will be assessed in children, adolescents, and young adults <25 years old with newly-diagnosed Ph+ (BCR::ABL1-rearranged) B acute lymphoblastic leukemia (B-ALL) who are treated with a modified Berlin-Frankfurt-Münster (mBFM) chemotherapy backbone that incorporates three cycles of blinatumomab without traditional consolidation chemotherapy in combination with continuous dasatinib. Will be estimated using the Kaplan-Meier method with standard errors of Peto.
Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years
ABL-class Ph-like B-ALL 3-year event free survival (EFS)
Tijdsspanne: Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years

Will be assessed in children, adolescents, and young adults <25 years old with newly-diagnosed ABL-class Ph-like B-ALL who are treated with a modified BFM chemotherapy backbone that incorporates three cycles of blinatumomab without traditional consolidation chemotherapy in combination with continuous imatinib for those with PDGFRB gene fusions or dasatinib for those without PDGFRB gene fusions. Will be estimated using the Kaplan-Meier method with standard errors of Peto.
Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years
Incidence of adverse events
Tijdsspanne: Up to 3 years

Will assess the safety and toxicity profile (infections, mucositis, neurotoxicity, cytokine release syndrome, hypogammaglobulinemia, therapy delays > 14 days, and treatment-related mortality) for patients with Ph+ or ABL-class Ph-like B-ALL treated on this novel chemo-immunotherapy backbone with continuous tyrosine kinase inhibitor (TKI). Will be assessed by the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.
Up to 3 years

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
3-year overall survival (OS)
Tijdsspanne: Time from enrollment to death from any cause or date of last contact for those who are alive, assessed up to 3 years

Will be assessed in patients with Ph+ and ABL-class Ph-like B-ALL, respectively. Will be estimated using the Kaplan-Meier method with standard errors of Peto.
Time from enrollment to death from any cause or date of last contact for those who are alive, assessed up to 3 years
3-year EFS
Tijdsspanne: Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years

Will be estimated using the Kaplan-Meier method with standard errors of Peto.
Time from enrollment to first event, relapse, second malignancy, or death in complete remission, or last contact for those who are event-free, assessed up to 3 years
3-year disease free survival
Tijdsspanne: Time from end of consolidation/blinatumomab block 2 (TP2) for early responders to first event (relapse, second malignancy, or death in complete remission) or last contact for those who are event-free, assessed up to 3 years

Will be estimated using the Kaplan-Meier method with standard errors of Peto.
Time from end of consolidation/blinatumomab block 2 (TP2) for early responders to first event (relapse, second malignancy, or death in complete remission) or last contact for those who are event-free, assessed up to 3 years
Cumulative incidence rates of relapse
Tijdsspanne: Up to 3 years

Will be estimated using Gray's method.
Up to 3 years
Treatment related mortality
Tijdsspanne: Up to 3 years

Will be estimated at the end of therapy.
Up to 3 years
OS of patients with ABL-class Ph-like B-ALL
Tijdsspanne: Time from enrollment to death from any cause or date of last contact for those who are alive, assessed up to 3 years

Will be stratified by their underlying ABL-class fusion subtypes.
Time from enrollment to death from any cause or date of last contact for those who are alive, assessed up to 3 years
Rates of end of Consolidation (EOC)/timepoint 2 (TP2) minimal residual disease (MRD) negativity for patients with Ph+ B-ALL
Tijdsspanne: From EOC to TP2

Defined as <1x10^-4 or <0.01% for patients with Ph+ B-ALL.
From EOC to TP2
Rates of EOC/TP2 MRD negativity for patients with ABL-class Ph-like B-ALL collectively and based on their ABL-class fusion subtypes
Tijdsspanne: From EOC to TP2

Defined as <1x10^-4 or <0.01% for patients with ABL-class Ph-like B-ALL collectively and based on their ABL-class fusion subtypes.
From EOC to TP2

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Rates of end of induction (EOI)/timepoint 1 (TP1) bone marrow MRD negativity with the introduction of dasatinib
Tijdsspanne: From EOI to TP1

Defined as <1x10-4 or <0.01% with the introduction of the relevant TKI during Induction for patients with Ph+ B-ALL.
From EOI to TP1
Outcomes of patients with Ph+ and Ph-like ABL-class B-ALL who are removed from protocol therapy due to consolidation failure
Tijdsspanne: Up to 3 years

Will be collected and described. A secondary analysis will also be conducted, examining the EFS of patients in both arms of the randomization using conventional definition of consolidation failure (EOC/TP2 MRD ≥ 1%).
Up to 3 years
Percentage of patients with Ph+ and ABL-class Ph-like B-ALL who continue TKI beyond protocol-prescribed therapy and their outcomes
Tijdsspanne: Up to 3 years

Will be collected and described.
Up to 3 years
Outcomes for patients with Ph+ and ABL-class Ph-like B-ALL who continue TKI beyond protocol-prescribed therapy
Tijdsspanne: Up to 3 years

EFS will be estimated at 3 years.
Up to 3 years
Prognostic significance of MRD by next-generation sequencing (NGS) at end of induction and end of consolidation
Tijdsspanne: Up to 3 years

Its association with outcomes will be explored.
Up to 3 years
Clinical characteristics and outcomes of patients with chronic myeloid leukemia-like biology
Tijdsspanne: Up to 3 years

Will be summarized using descriptive statistics.
Up to 3 years
Immune function of Ph+ and ABL-class Ph-like B-ALL patients
Tijdsspanne: Up to 3 years

Will be summarized using descriptive statistics.
Up to 3 years
TKI levels in the plasma and cerebrospinal fluid of children with Ph+ and ABL-class Ph-like B-ALL
Tijdsspanne: Up to 3 years

Will be summarized using descriptive statistics.
Up to 3 years
Impact of TKIs and high-dose methotrexate interaction and identify clinical and biologic factors influencing methotrexate clearance
Tijdsspanne: Up to 3 years

Will be assessed by summarizing frequencies observed of the same.
Up to 3 years

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

National Cancer Institute (NCI)

Onderzoekers

  • Hoofdonderzoeker: Thai Hoa Tran, Children's Oncology Group

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

30 mei 2025

Primaire voltooiing (Geschat)

1 december 2030

Studie voltooiing (Geschat)

1 december 2030

Studieregistratiedata

Eerst ingediend

8 november 2023

Eerst ingediend dat voldeed aan de QC-criteria

8 november 2023

Eerst geplaatst (Werkelijk)

9 november 2023

Updates van studierecords

Laatste update geplaatst (Werkelijk)

27 oktober 2026

Laatste update ingediend die voldeed aan QC-criteria

24 oktober 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • NCI-2023-09214
  • U10CA180886 (Subsidie/contract van de Amerikaanse NIH)
  • NCI-2023-09214 (Register-ID: CTRP (Clinical Trial Reporting Program))
  • AALL2131 (Andere identificatie: CTEP)
  • AALL2131 (Andere identificatie: Children's Oncology Group)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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