- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT04759586
- Oryginalna próba
Niwolumab w skojarzeniu z chemioimmunoterapią w leczeniu nowo rozpoznanego pierwotnego chłoniaka B-komórkowego śródpiersia
Randomizowane badanie fazy 3 niwolumabu (NSC nr 748726) w skojarzeniu z chemioterapią w leczeniu nowo rozpoznanego pierwotnego chłoniaka z komórek B śródpiersia
This phase III trial compares the effects of nivolumab with chemo-immunotherapy versus chemo-immunotherapy alone in treating patients with newly diagnosed primary mediastinal B-cell lymphoma (PMBCL). Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of cancer cells to grow and spread. Treatment for PMBCL involves chemotherapy combined with an immunotherapy called rituximab. Chemotherapy drugs work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Giving nivolumab with chemo-immunotherapy may help treat patients with PMBCL.
Przegląd badań
Status
Interwencja / Leczenie
- Lek: Cyclophosphamide
- Lek: Doxorubicin Hydrochloride
- Lek: Prednisone
- Biologiczny: Rituximab
- Lek: Vincristine Sulfate
- Procedura: Echocardiography Test
- Biologiczny: Nivolumab
- Procedura: Computed Tomography
- Procedura: Positron Emission Tomography
- Lek: Etoposide Phosphate
- Biologiczny: Filgrastim
- Procedura: Bone Marrow Aspiration
- Procedura: Bone Marrow Biopsy
- Promieniowanie: Radiation Therapy
- Lek: Prednisolone
- Biologiczny: Pegfilgrastim
- Procedura: Lumbar Puncture
- Procedura: Biospecimen Collection
- Biologiczny: Rituximab and Hyaluronidase Human
Szczegółowy opis
PRIMARY OBJECTIVE:
I. To determine if nivolumab + chemo-immunotherapy results in a superior long term progression-free survival (PFS) (events defined as disease progression confirmed by central review or death) when compared with chemo-immunotherapy alone in patients with newly diagnosed primary mediastinal B-cell lymphoma.
SECONDARY OBJECTIVES:
I. To compare the rates of "efficacy-related event-free survival (EFS)" (eEFS) (events defined as progression, change in therapy due to finding that led to concern about efficacy, biopsy + disease after 6 cycles of therapy, or death) between chemo-immunotherapy alone and chemo-immunotherapy + nivolumab in patients with newly diagnosed PMBCL.
II. To compare the rates of "therapy-related EFS" (tEFS) (events defined as relapse/progression, change in therapy for any reason, biopsy + disease after 6 cycles of therapy, secondary malignancy [SMN] or death) between chemo-immunotherapy alone and chemo-immunotherapy + nivolumab in patients with newly diagnosed PMBCL.
III. To compare the rates of overall survival (OS) between chemo-immunotherapy alone and chemo-immunotherapy + nivolumab in patients with newly diagnosed PMBCL.
IV. To establish the rate of a positive positron emission tomography (PET)-computed tomography (CT) (defined as Deauville score 4 or 5) at the completion of 6 cycles of nivolumab + rituximab (R)- cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP)/dose-adjusted (DA)-etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (EPOCH)-R and R-CHOP/DA-EPOCH-R in patients with newly diagnosed PMBCL and evaluate the prognostic significance of such a finding.
EXPLORATORY OBJECTIVES:
I. To bank radiology images for further studies. II. To bank specimens for future correlative studies. III. Characterize the immune profile of patients treated with nivolumab + chemo-immunotherapy to identify markers predictive of response.
IV. Define the rate of complete response at the completion of initial planned therapy.
OUTLINE: Patients are randomly assigned to backbone therapy or backbone therapy + nivolumab within each of 6 strata. The strata are determined by physician's choice of backbone (DA-EPOCH-R versus [vs.] R-CHOP vs. R-CHOP + RT) and whether or not the patient had 1 prior cycle of therapy.
ARM A (DA-EPOCH-R): Patients receive prednisone or prednisolone orally (PO) once daily (QD) on days 1-5 and rituximab intravenously (IV) or rituximab and hyaluronidase human subcutaneously (SC) over 5 minutes on day 1 or 5. Patients also receive etoposide phosphate, doxorubicin hydrochloride, and vincristine sulfate IV over 96 hours on days 1-4 and cyclophosphamide IV over 30-60 minutes on day 5. Beginning 24-72 hours after completing cyclophosphamide, patients receive filgrastim or pegylated filgrastim SC daily until absolute neutrophil count (ANC) is >= 500/uL after the expected nadir. Treatment repeats every 21 days for up to 6 cycles (5 if the patient had 1 prior cycle of treatment) in the absence of disease progression or unacceptable toxicity. Patients undergo echocardiography (ECHO) during screening and as clinically indicated and a lumbar puncture (LP) for cerebral spinal fluid (CSF) collection optionally during screening. Patients also undergo computed tomography (CT) or positron emission tomography (PET)/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
ARM B (DA-EPOCH-R + NIVOLUMAB): Patients receive treatment as in Arm A. Patients also receive nivolumab IV over 30 minutes on day 1. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
ARM C (R-CHOP): Patients receive prednisone or prednisolone PO QD on days 1-5 and rituximab IV or rituximab and hyaluronidase human SC over 5 minutes on day 1 or 5. Patients also receive cyclophosphamide IV over 30-60 minutes, doxorubicin hydrochloride IV over 1-15 minutes or up to 60 minutes, and vincristine sulfate IV over 1 or up to 60 minutes on day 1. Treatment repeats every 21 days for up to 6 cycles (5 if the patient had 1 prior cycle of treatment) in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
ARM D (R-CHOP + NIVOLUMAB): Patients receive treatment as in Arm C. Patients also receive nivolumab IV over 30 minutes on day 1. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
ARM E (R-CHOP + RADIOTHERAPY): Patients receive treatment as in Arm C. Within 6-8 weeks after completion of chemotherapy, patients undergo radiation therapy over 25 fractions. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
ARM F (R-CHOP + RADIOTHERAPY + NIVOLUMAB): Patients receive treatment as in Arm D. Within 6-8 weeks after completion of chemotherapy, patients undergo radiation therapy over 25 fractions. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study.
After completion of study treatment, patients are followed up every 3 months for year 1, every 6 months for years 2-3, and annually thereafter.
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 3
Kontakty i lokalizacje
Lokalizacje studiów
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New South Wales
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Hunter Regional Mail Centre, New South Wales, Australia, 2310
- John Hunter Children's Hospital
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Westmead, New South Wales, Australia, 2145
- The Children's Hospital at Westmead
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Queensland
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South Brisbane, Queensland, Australia, 4101
- Queensland Children's Hospital
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Victoria
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Parkville, Victoria, Australia, 3052
- Royal Children's Hospital
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Western Australia
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Perth, Western Australia, Australia, 6009
- Perth Children's Hospital
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-
-
-
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Québec, Kanada, G1V 4G2
- CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL)
-
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Alberta
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Edmonton, Alberta, Kanada, T6G 2B7
- University of Alberta Hospital
-
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Manitoba
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Winnipeg, Manitoba, Kanada, R3E 0V9
- CancerCare Manitoba
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Newfoundland and Labrador
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St. John's, Newfoundland and Labrador, Kanada, A1B 3V6
- Janeway Child Health Centre
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3K 6R8
- IWK Health Centre
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Ontario
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Hamilton, Ontario, Kanada, L8N 3Z5
- McMaster Children's Hospital at Hamilton Health Sciences
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London, Ontario, Kanada, N6A 5W9
- Children's Hospital
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Ottawa, Ontario, Kanada, K1H 8L1
- Children's Hospital of Eastern Ontario
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Toronto, Ontario, Kanada, M5G 1X8
- Hospital for Sick Children
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Quebec
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Montreal, Quebec, Kanada, H3H 1P3
- The Montreal Children's Hospital of the MUHC
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Montreal, Quebec, Kanada, H3T 1C5
- Centre Hospitalier Universitaire Sainte-Justine
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Sherbrooke, Quebec, Kanada, J1H 5N4
- Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
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-
-
-
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Caguas, Portoryko, 00726
- HIMA San Pablo Oncologic Hospital
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-
-
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Alabama
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Birmingham, Alabama, Stany Zjednoczone, 35233
- Children's Hospital of Alabama
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Mobile, Alabama, Stany Zjednoczone, 36604
- USA Health Strada Patient Care Center
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Alaska
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Anchorage, Alaska, Stany Zjednoczone, 99508
- Providence Alaska Medical Center
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Arizona
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Mesa, Arizona, Stany Zjednoczone, 85202
- Banner Children's at Desert
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Tucson, Arizona, Stany Zjednoczone, 85719
- Banner University Medical Center - Tucson
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Arkansas
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Little Rock, Arkansas, Stany Zjednoczone, 72202-3591
- Arkansas Children's Hospital
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California
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Costa Mesa, California, Stany Zjednoczone, 92627
- UC Irvine Health Cancer Center-Newport
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Downey, California, Stany Zjednoczone, 90242
- Kaiser Permanente Downey Medical Center
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Duarte, California, Stany Zjednoczone, 91010
- City of Hope Comprehensive Cancer Center
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Irvine, California, Stany Zjednoczone, 92618
- City of Hope at Irvine Lennar
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Irvine, California, Stany Zjednoczone, 92612
- UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care
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Loma Linda, California, Stany Zjednoczone, 92354
- Loma Linda University Medical Center
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Long Beach, California, Stany Zjednoczone, 90806
- Miller Children's and Women's Hospital Long Beach
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Los Angeles, California, Stany Zjednoczone, 90048
- Cedars-Sinai Medical Center
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Los Angeles, California, Stany Zjednoczone, 90027
- Children's Hospital Los Angeles
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Los Angeles, California, Stany Zjednoczone, 90095
- Mattel Children's Hospital UCLA
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Madera, California, Stany Zjednoczone, 93636
- Valley Children's Hospital
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Oakland, California, Stany Zjednoczone, 94611
- Kaiser Permanente-Oakland
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Orange, California, Stany Zjednoczone, 92868
- UC Irvine Health/Chao Family Comprehensive Cancer Center
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Orange, California, Stany Zjednoczone, 92868
- Children's Hospital of Orange County
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Palo Alto, California, Stany Zjednoczone, 94304
- Lucile Packard Children's Hospital Stanford University
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Sacramento, California, Stany Zjednoczone, 95817
- University of California Davis Comprehensive Cancer Center
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San Diego, California, Stany Zjednoczone, 92123
- Rady Children's Hospital - San Diego
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Colorado
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Aurora, Colorado, Stany Zjednoczone, 80045
- Children's Hospital Colorado
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Denver, Colorado, Stany Zjednoczone, 80218
- Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center
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Connecticut
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Hartford, Connecticut, Stany Zjednoczone, 06106
- Connecticut Children's Medical Center
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Delaware
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Wilmington, Delaware, Stany Zjednoczone, 19803
- Alfred I duPont Hospital for Children
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District of Columbia
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Washington D.C., District of Columbia, Stany Zjednoczone, 20010
- Children's National Medical Center
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Washington D.C., District of Columbia, Stany Zjednoczone, 20007
- MedStar Georgetown University Hospital
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Florida
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Fort Lauderdale, Florida, Stany Zjednoczone, 33316
- Broward Health Medical Center
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Fort Myers, Florida, Stany Zjednoczone, 33908
- Golisano Children's Hospital of Southwest Florida
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Gainesville, Florida, Stany Zjednoczone, 32610
- UF Health Cancer Institute - Gainesville
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Hollywood, Florida, Stany Zjednoczone, 33021
- Memorial Regional Hospital/Joe DiMaggio Children's Hospital
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Jacksonville, Florida, Stany Zjednoczone, 32207
- Nemours Children's Clinic-Jacksonville
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Miami, Florida, Stany Zjednoczone, 33136
- University of Miami Miller School of Medicine-Sylvester Cancer Center
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Orlando, Florida, Stany Zjednoczone, 32827
- Nemours Children's Hospital
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Orlando, Florida, Stany Zjednoczone, 32806
- Arnold Palmer Hospital for Children
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St. Petersburg, Florida, Stany Zjednoczone, 33701
- Johns Hopkins All Children's Hospital
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Tampa, Florida, Stany Zjednoczone, 33606
- Tampa General Hospital
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Tampa, Florida, Stany Zjednoczone, 33607
- Saint Joseph's Hospital/Children's Hospital-Tampa
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Georgia
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Atlanta, Georgia, Stany Zjednoczone, 30308
- Emory University Hospital Midtown
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Atlanta, Georgia, Stany Zjednoczone, 30322
- Emory University Hospital/Winship Cancer Institute
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Atlanta, Georgia, Stany Zjednoczone, 30342
- Emory Saint Joseph's Hospital
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Atlanta, Georgia, Stany Zjednoczone, 30308
- Emory Proton Therapy Center
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Atlanta, Georgia, Stany Zjednoczone, 30329
- Children's Healthcare of Atlanta - Arthur M Blank Hospital
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Savannah, Georgia, Stany Zjednoczone, 31404
- Memorial Health University Medical Center
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Hawaii
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Honolulu, Hawaii, Stany Zjednoczone, 96826
- Kapiolani Medical Center for Women and Children
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Idaho
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Boise, Idaho, Stany Zjednoczone, 83712
- Saint Luke's Cancer Institute - Boise
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Illinois
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Aurora, Illinois, Stany Zjednoczone, 60504
- Rush-Copley Medical Center
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Chicago, Illinois, Stany Zjednoczone, 60611
- Northwestern University
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Chicago, Illinois, Stany Zjednoczone, 60637
- University of Chicago Comprehensive Cancer Center
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Chicago, Illinois, Stany Zjednoczone, 60612
- University of Illinois
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Chicago, Illinois, Stany Zjednoczone, 60611
- Lurie Children's Hospital-Chicago
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Danville, Illinois, Stany Zjednoczone, 61832
- Carle at The Riverfront
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DeKalb, Illinois, Stany Zjednoczone, 60115
- Northwestern Medicine Cancer Center Kishwaukee
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Decatur, Illinois, Stany Zjednoczone, 62526
- Decatur Memorial Hospital
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Effingham, Illinois, Stany Zjednoczone, 62401
- Carle Physician Group-Effingham
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Geneva, Illinois, Stany Zjednoczone, 60134
- Northwestern Medicine Cancer Center Delnor
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Lake Forest, Illinois, Stany Zjednoczone, 60045
- Northwestern Medicine Lake Forest Hospital
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Mattoon, Illinois, Stany Zjednoczone, 61938
- Carle Physician Group-Mattoon/Charleston
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Maywood, Illinois, Stany Zjednoczone, 60153
- Loyola University Medical Center
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O'Fallon, Illinois, Stany Zjednoczone, 62269
- HSHS Saint Elizabeth's Hospital
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Oak Lawn, Illinois, Stany Zjednoczone, 60453
- Advocate Children's Hospital-Oak Lawn
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Park Ridge, Illinois, Stany Zjednoczone, 60068
- Advocate Children's Hospital-Park Ridge
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Peoria, Illinois, Stany Zjednoczone, 61637
- OSF Children's Hospital of Illinois
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Springfield, Illinois, Stany Zjednoczone, 62702
- Southern Illinois University School of Medicine
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Springfield, Illinois, Stany Zjednoczone, 62702
- Springfield Clinic
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Springfield, Illinois, Stany Zjednoczone, 62781
- Springfield Memorial Hospital
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Urbana, Illinois, Stany Zjednoczone, 61801
- Carle Cancer Center
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Warrenville, Illinois, Stany Zjednoczone, 60555
- Northwestern Medicine Cancer Center Warrenville
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Indiana
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Indianapolis, Indiana, Stany Zjednoczone, 46202
- Riley Hospital for Children
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Richmond, Indiana, Stany Zjednoczone, 47374
- Reid Health
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Iowa
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Ankeny, Iowa, Stany Zjednoczone, 50023
- UI Health Care Mission Cancer and Blood - Ankeny Clinic
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Clive, Iowa, Stany Zjednoczone, 50325
- UI Health Care Mission Cancer and Blood - West Des Moines Clinic
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Des Moines, Iowa, Stany Zjednoczone, 50314
- Mercy Medical Center - Des Moines
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Des Moines, Iowa, Stany Zjednoczone, 50309
- Blank Children's Hospital
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Des Moines, Iowa, Stany Zjednoczone, 50314
- UI Health Care Mission Cancer and Blood - Laurel Clinic
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Iowa City, Iowa, Stany Zjednoczone, 52242
- University of Iowa/Holden Comprehensive Cancer Center
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Sioux City, Iowa, Stany Zjednoczone, 51101
- Siouxland Regional Cancer Center
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Waukee, Iowa, Stany Zjednoczone, 50263
- UI Health Care Mission Cancer and Blood - Waukee Clinic
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Kansas
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Wichita, Kansas, Stany Zjednoczone, 67214
- Wesley Medical Center
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Kentucky
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Lexington, Kentucky, Stany Zjednoczone, 40536
- University of Kentucky/Markey Cancer Center
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Louisville, Kentucky, Stany Zjednoczone, 40202
- Norton Children's Hospital
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Louisiana
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New Orleans, Louisiana, Stany Zjednoczone, 70121
- Ochsner Medical Center Jefferson
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New Orleans, Louisiana, Stany Zjednoczone, 70118
- Children's Hospital New Orleans
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Maine
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Bangor, Maine, Stany Zjednoczone, 04401
- Eastern Maine Medical Center
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Scarborough, Maine, Stany Zjednoczone, 04074
- Maine Children's Cancer Program
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Maryland
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Baltimore, Maryland, Stany Zjednoczone, 21287
- Johns Hopkins University/Sidney Kimmel Cancer Center
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Baltimore, Maryland, Stany Zjednoczone, 21215
- Sinai Hospital of Baltimore
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Baltimore, Maryland, Stany Zjednoczone, 21204
- Greater Baltimore Medical Center
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Baltimore, Maryland, Stany Zjednoczone, 21201
- University of Maryland/Greenebaum Cancer Center
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Bethesda, Maryland, Stany Zjednoczone, 20889-5600
- Walter Reed National Military Medical Center
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Massachusetts
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Boston, Massachusetts, Stany Zjednoczone, 02215
- Dana-Farber Cancer Institute
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Boston, Massachusetts, Stany Zjednoczone, 02111
- Tufts Medical Center
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Michigan
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Ann Arbor, Michigan, Stany Zjednoczone, 48109
- C S Mott Children's Hospital
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Detroit, Michigan, Stany Zjednoczone, 48202
- Henry Ford Hospital
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Detroit, Michigan, Stany Zjednoczone, 48201
- Children's Hospital of Michigan
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East Lansing, Michigan, Stany Zjednoczone, 48823
- Michigan State University
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Grand Rapids, Michigan, Stany Zjednoczone, 49503
- Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
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Kalamazoo, Michigan, Stany Zjednoczone, 49007
- Bronson Methodist Hospital
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Niles, Michigan, Stany Zjednoczone, 49120
- Corewell Health Lakeland Hospitals - Niles Hospital
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Royal Oak, Michigan, Stany Zjednoczone, 48073
- Corewell Health Children's
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Minnesota
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Burnsville, Minnesota, Stany Zjednoczone, 55337
- Minnesota Oncology - Burnsville
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Coon Rapids, Minnesota, Stany Zjednoczone, 55433
- Mercy Hospital
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Edina, Minnesota, Stany Zjednoczone, 55435
- Fairview Southdale Hospital
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Fridley, Minnesota, Stany Zjednoczone, 55432
- Unity Hospital
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Maplewood, Minnesota, Stany Zjednoczone, 55109
- Minnesota Oncology Hematology PA-Maplewood
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Minneapolis, Minnesota, Stany Zjednoczone, 55404
- Children's Hospitals and Clinics of Minnesota - Minneapolis
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Minneapolis, Minnesota, Stany Zjednoczone, 55407
- Abbott-Northwestern Hospital
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Saint Louis Park, Minnesota, Stany Zjednoczone, 55416
- Park Nicollet Clinic - Saint Louis Park
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Saint Paul, Minnesota, Stany Zjednoczone, 55102
- United Hospital
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Mississippi
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Jackson, Mississippi, Stany Zjednoczone, 39216
- University of Mississippi Medical Center
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Missouri
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Chesterfield, Missouri, Stany Zjednoczone, 63017
- Saint Luke's Hospital
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City of Saint Peters, Missouri, Stany Zjednoczone, 63376
- Siteman Cancer Center at Saint Peters Hospital
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Creve Coeur, Missouri, Stany Zjednoczone, 63141
- Siteman Cancer Center at West County Hospital
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Kansas City, Missouri, Stany Zjednoczone, 64108
- Children's Mercy Hospitals and Clinics
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St Louis, Missouri, Stany Zjednoczone, 63110
- Washington University School of Medicine
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St Louis, Missouri, Stany Zjednoczone, 63129
- Siteman Cancer Center-South County
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St Louis, Missouri, Stany Zjednoczone, 63136
- Siteman Cancer Center at Christian Hospital
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St Louis, Missouri, Stany Zjednoczone, 63141
- Mercy Hospital Saint Louis
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Nebraska
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Omaha, Nebraska, Stany Zjednoczone, 68198
- University of Nebraska Medical Center
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Omaha, Nebraska, Stany Zjednoczone, 68114
- Children's Hospital and Medical Center of Omaha
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Nevada
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Las Vegas, Nevada, Stany Zjednoczone, 89135
- Alliance for Childhood Diseases/Cure 4 the Kids Foundation
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Reno, Nevada, Stany Zjednoczone, 89502
- Renown Regional Medical Center
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New Hampshire
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Lebanon, New Hampshire, Stany Zjednoczone, 03756
- Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
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New Jersey
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Basking Ridge, New Jersey, Stany Zjednoczone, 07920
- Memorial Sloan Kettering Basking Ridge
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Hackensack, New Jersey, Stany Zjednoczone, 07601
- Hackensack University Medical Center
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Middletown, New Jersey, Stany Zjednoczone, 07748
- Memorial Sloan Kettering Monmouth
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Montvale, New Jersey, Stany Zjednoczone, 07645
- Memorial Sloan Kettering Bergen
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Morristown, New Jersey, Stany Zjednoczone, 07960
- Morristown Medical Center
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New Brunswick, New Jersey, Stany Zjednoczone, 08903
- Rutgers Cancer Institute of New Jersey
-
New Brunswick, New Jersey, Stany Zjednoczone, 08903
- Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital
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Paterson, New Jersey, Stany Zjednoczone, 07503
- Saint Joseph's Regional Medical Center
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New Mexico
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Albuquerque, New Mexico, Stany Zjednoczone, 87106
- Presbyterian Hospital
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New York
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Albany, New York, Stany Zjednoczone, 12208
- Albany Medical Center
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Buffalo, New York, Stany Zjednoczone, 14263
- Roswell Park Cancer Institute
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Commack, New York, Stany Zjednoczone, 11725
- Memorial Sloan Kettering Commack
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Harrison, New York, Stany Zjednoczone, 10604
- Memorial Sloan Kettering Westchester
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New Hyde Park, New York, Stany Zjednoczone, 11040
- The Steven and Alexandra Cohen Children's Medical Center of New York
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New York, New York, Stany Zjednoczone, 10065
- Memorial Sloan Kettering Cancer Center
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New York, New York, Stany Zjednoczone, 10032
- NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
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New York, New York, Stany Zjednoczone, 10065
- NYP/Weill Cornell Medical Center
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Rochester, New York, Stany Zjednoczone, 14642
- University of Rochester
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Stony Brook, New York, Stany Zjednoczone, 11794
- Stony Brook University Medical Center
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Syracuse, New York, Stany Zjednoczone, 13210
- State University of New York Upstate Medical University
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The Bronx, New York, Stany Zjednoczone, 10467
- Montefiore Medical Center - Moses Campus
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Uniondale, New York, Stany Zjednoczone, 11553
- Memorial Sloan Kettering Nassau
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Valhalla, New York, Stany Zjednoczone, 10595
- New York Medical College
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Webster, New York, Stany Zjednoczone, 14580
- Wilmot Cancer Institute at Webster
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North Carolina
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Asheville, North Carolina, Stany Zjednoczone, 28801
- Mission Hospital
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Asheville, North Carolina, Stany Zjednoczone, 28803
- AdventHealth Infusion Center Asheville
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Charlotte, North Carolina, Stany Zjednoczone, 28203
- Carolinas Medical Center/Levine Cancer Institute
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Charlotte, North Carolina, Stany Zjednoczone, 28204
- Novant Health Presbyterian Medical Center
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Greenville, North Carolina, Stany Zjednoczone, 27834
- East Carolina University
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Hendersonville, North Carolina, Stany Zjednoczone, 28792
- AdventHealth Hendersonville
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Winston-Salem, North Carolina, Stany Zjednoczone, 27157
- Wake Forest University Health Sciences
-
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North Dakota
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Fargo, North Dakota, Stany Zjednoczone, 58122
- Sanford Broadway Medical Center
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Ohio
-
Akron, Ohio, Stany Zjednoczone, 44308
- Children's Hospital Medical Center of Akron
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Cincinnati, Ohio, Stany Zjednoczone, 45229
- Cincinnati Children's Hospital Medical Center
-
Cleveland, Ohio, Stany Zjednoczone, 44195
- Cleveland Clinic Foundation
-
Cleveland, Ohio, Stany Zjednoczone, 44106
- Rainbow Babies and Childrens Hospital
-
Columbus, Ohio, Stany Zjednoczone, 43205
- Nationwide Children's Hospital
-
Dayton, Ohio, Stany Zjednoczone, 45404
- Dayton Children's Hospital
-
Dayton, Ohio, Stany Zjednoczone, 45415
- Dayton Physician LLC - Englewood
-
Kettering, Ohio, Stany Zjednoczone, 45429
- Kettering Medical Center
-
Kettering, Ohio, Stany Zjednoczone, 45409
- Greater Dayton Cancer Center
-
Toledo, Ohio, Stany Zjednoczone, 43606
- ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
-
-
Oklahoma
-
Oklahoma City, Oklahoma, Stany Zjednoczone, 73104
- University of Oklahoma Health Sciences Center
-
-
Oregon
-
Portland, Oregon, Stany Zjednoczone, 97239
- Oregon Health and Science University
-
Portland, Oregon, Stany Zjednoczone, 97227
- Legacy Emanuel Children's Hospital
-
-
Pennsylvania
-
Allentown, Pennsylvania, Stany Zjednoczone, 18103
- Lehigh Valley Hospital-Cedar Crest
-
Danville, Pennsylvania, Stany Zjednoczone, 17822
- Geisinger Medical Center
-
Hershey, Pennsylvania, Stany Zjednoczone, 17033
- Penn State Children's Hospital
-
Philadelphia, Pennsylvania, Stany Zjednoczone, 19104
- Children's Hospital of Philadelphia
-
Philadelphia, Pennsylvania, Stany Zjednoczone, 19134
- Saint Christopher's Hospital for Children
-
Pittsburgh, Pennsylvania, Stany Zjednoczone, 15224
- Children's Hospital of Pittsburgh of UPMC
-
-
Rhode Island
-
Providence, Rhode Island, Stany Zjednoczone, 02903
- Rhode Island Hospital
-
-
South Carolina
-
Columbia, South Carolina, Stany Zjednoczone, 29203
- Prisma Health Richland Hospital
-
Greenville, South Carolina, Stany Zjednoczone, 29607
- Saint Francis Cancer Center
-
Greenville, South Carolina, Stany Zjednoczone, 29615
- Prisma Health Cancer Institute - Eastside
-
Greenville, South Carolina, Stany Zjednoczone, 29601
- Saint Francis Hospital
-
Greenville, South Carolina, Stany Zjednoczone, 29605
- BI-LO Charities Children's Cancer Center
-
-
South Dakota
-
Sioux Falls, South Dakota, Stany Zjednoczone, 57117-5134
- Sanford USD Medical Center - Sioux Falls
-
-
Tennessee
-
Knoxville, Tennessee, Stany Zjednoczone, 37916
- East Tennessee Childrens Hospital
-
Memphis, Tennessee, Stany Zjednoczone, 38105
- Saint Jude Children's Research Hospital
-
Nashville, Tennessee, Stany Zjednoczone, 37232
- Vanderbilt University/Ingram Cancer Center
-
Nashville, Tennessee, Stany Zjednoczone, 37203
- The Children's Hospital at TriStar Centennial
-
-
Texas
-
Amarillo, Texas, Stany Zjednoczone, 79106
- Texas Tech University Health Sciences Center-Amarillo
-
Austin, Texas, Stany Zjednoczone, 78723
- Dell Children's Medical Center of Central Texas
-
Corpus Christi, Texas, Stany Zjednoczone, 78411
- Driscoll Children's Hospital
-
Dallas, Texas, Stany Zjednoczone, 75390
- UT Southwestern/Simmons Cancer Center-Dallas
-
Dallas, Texas, Stany Zjednoczone, 75230
- Medical City Dallas Hospital
-
El Paso, Texas, Stany Zjednoczone, 79905
- El Paso Children's Hospital
-
Houston, Texas, Stany Zjednoczone, 77030
- UT MD Anderson Cancer Center
-
Houston, Texas, Stany Zjednoczone, 77030
- Houston Methodist Hospital
-
Houston, Texas, Stany Zjednoczone, 77030
- Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
-
Lubbock, Texas, Stany Zjednoczone, 79410
- Covenant Children's Hospital
-
Lubbock, Texas, Stany Zjednoczone, 79415
- UMC Cancer Center / UMC Health System
-
San Antonio, Texas, Stany Zjednoczone, 78229
- University of Texas Health Science Center at San Antonio
-
San Antonio, Texas, Stany Zjednoczone, 78207
- Children's Hospital of San Antonio
-
San Antonio, Texas, Stany Zjednoczone, 78229
- Methodist Children's Hospital of South Texas
-
-
Utah
-
Salt Lake City, Utah, Stany Zjednoczone, 84113
- Primary Children's Hospital
-
-
Virginia
-
Charlottesville, Virginia, Stany Zjednoczone, 22908
- University of Virginia Cancer Center
-
Falls Church, Virginia, Stany Zjednoczone, 22042
- Inova Fairfax Hospital
-
Norfolk, Virginia, Stany Zjednoczone, 23507
- Children's Hospital of The King's Daughters
-
Richmond, Virginia, Stany Zjednoczone, 23298
- VCU Massey Comprehensive Cancer Center
-
Roanoke, Virginia, Stany Zjednoczone, 24014
- Carilion Children's
-
-
Washington
-
Renton, Washington, Stany Zjednoczone, 98055
- Valley Medical Center
-
Seattle, Washington, Stany Zjednoczone, 98105
- Seattle Children's Hospital
-
Spokane, Washington, Stany Zjednoczone, 99204
- Providence Sacred Heart Medical Center and Children's Hospital
-
Tacoma, Washington, Stany Zjednoczone, 98405
- Mary Bridge Children's Hospital and Health Center
-
Tacoma, Washington, Stany Zjednoczone, 98431
- Madigan Army Medical Center
-
-
West Virginia
-
Charleston, West Virginia, Stany Zjednoczone, 25304
- Vandalia Health/CAMC Institute for Academic Medicine
-
-
Wisconsin
-
Madison, Wisconsin, Stany Zjednoczone, 53792
- University of Wisconsin Carbone Cancer Center - University Hospital
-
Marshfield, Wisconsin, Stany Zjednoczone, 54449
- Marshfield Medical Center-Marshfield
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
-
Age >= 2 years
-
Patient must have histologically confirmed primary mediastinal B-cell lymphoma (PMBCL) as defined by World Health Organization (WHO) criteria
-
Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 or ECOG performance status of 3 if poor performance is related to lymphoma
- Children's Oncology Group (COG) Institutions: Use Karnofsky for patients >= 17 and < 18 years of age and Lansky for patients < 17 years of age
-
Adults (age 18 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 actual body weight
-
Pediatric Patients (age < 18 years): The following must have been obtained within 14 days prior to registration:
-
Measured or calculated (based on institutional standard) creatinine clearance or radioisotope glomerular filtration rate (GFR) >= 70 ml/min/1.73 m^2, or
-
Serum creatinine =< 1.5 x institutional upper limit of normal (IULN), or a serum creatinine based on age/sex as follows:
- Age : 2 to < 6 year; Maximum serum creatinine (mg/dL): 0.8 (male; 0.8 (female)
- Age : 6 to < 10 years; Maximum serum creatinine (mg/dL): 1 (male); 1 (female)
- Age : 10 to < 13 years; Maximum serum creatinine (mg/dL): 1.2 (male); 1.2 (female)
- Age : 13 to < 16 years; Maximum serum creatinine (mg/dL): 1.5 (male); 1.4 (female)
- Age : >= 16 years to < 18 years; Maximum serum creatinine (mg/dL): 1.7 (male); 1.4 (female)
-
-
Patients with abnormal liver function will be eligible to enroll if the lab abnormality is thought to be due to the lymphoma or Gilbert's syndrome
-
Age >= 18 years: Ejection fraction of >= 50% by echocardiogram
-
Age < 18 years: Shortening fraction of >= 27% by echocardiogram, or ejection fraction of >= 50% by radionuclide angiogram
-
Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
-
For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated
-
Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load
-
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
Exclusion Criteria:
-
Administration of prior anti-cancer therapy except as outlined below:
- A short course (=< 2 weeks) of corticosteroids for the relief of lymphoma-related symptoms
- A single course of COP (cyclophosphamide, vincristine, and prednisone)
- One cycle of chemo-immunotherapy including R-CHOP, DA-EPOCH-R, a pediatric mature B-cell non-Hodgkin lymphoma (B-NHL) induction therapy (such as ANHL1131), or intrathecal chemotherapy that has not started more than 21 days prior to enrollment
-
Active ischemic heart disease or heart failure
-
Active uncontrolled infection
-
Central nervous system (CNS) involvement of lymphoma
-
Patients with a prior or concurrent malignancy whose natural history or treatment has the potential to interfere with safety or efficacy assessment of this trial
-
Active autoimmune disease that has required systemic treatment (such as disease modifying agents, corticosteroids, or immunosuppressive agents) in the past 2 years. Replacement therapy such as thyroxine, insulin or physiologic corticosteroid for adrenal or pituitary insufficiency is not considered a form of systemic treatment
-
In patients < 18 years of age hepatitis B serologies consistent with past or current infections
-
Patients with severe hepatic impairment (Child-Pugh class C or serum total bilirubin > 5.0 mg/dL) unless thought to be due to lymphoma or Gilbert's syndrome
-
Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A pregnancy test is required for female patients of childbearing potential
-
Sexually active patients of reproductive potential who have not agreed to use a highly effective contraceptive method (failure rate of < 1% per year when used consistently and correctly) for the duration of their study participation
-
Lactating females are not eligible unless they have agreed not to breastfeed their infants starting with the first dose of study therapy and for at least 6 months after the last dose of rituximab
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Aktywny komparator: Arm A (DA-EPOCH-R)
See Detailed Description |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Given IV
Inne nazwy:
Given SC
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Given PO
Inne nazwy:
Given SC
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
|
Eksperymentalny: Arm B (DA-EPOCH-R, nivolumab)
Patients receive treatment as in Arm A. Patients also receive nivolumab IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 6 cycles (5 if the patient had 1 prior cycle of treatment) in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO and LP for CSF collection during screening. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study. |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Given IV
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Given IV
Inne nazwy:
Given SC
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Given PO
Inne nazwy:
Given SC
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
|
Aktywny komparator: Arm C (R-CHOP)
Patients receive prednisone or prednisolone PO QD on days 1-5 and rituximab IV or rituximab and hyaluronidase human SC over 5 minutes on day 1 or 5. Patients also receive cyclophosphamide IV over 30-60 minutes, doxorubicin hydrochloride IV over 1-15 minutes or up to 60 minutes, and vincristine sulfate IV over 1 or up to 60 minutes on day 1. Treatment repeats every 21 days for up to 6 cycles (5 if the patient had 1 prior cycle of treatment) in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study. |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Given PO
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
|
Eksperymentalny: Arm D (R-CHOP, nivolumab)
Patients receive treatment as in Arm C. Patients also receive nivolumab IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 6 cycles (5 if the patient had 1 prior cycle of treatment) in the absence of disease progression or unacceptable toxicity. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study. |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Given IV
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Given PO
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
|
Aktywny komparator: Arm E (R-CHOP, radiation therapy)
Patients receive treatment as in Arm C. Within 6-8 weeks after completion of chemotherapy, patients undergo radiation therapy over 25 fractions. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study. |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Undergo radiation therapy
Inne nazwy:
Given PO
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
|
Eksperymentalny: Arm F (R-CHOP, nivolumab, radiation therapy)
Patients receive treatment as in Arm D. Within 6-8 weeks after completion of chemotherapy, patients undergo radiation therapy over 25 fractions. Patients undergo ECHO during screening and as clinically indicated and LP for CSF collection optionally during screening. Patients also undergo CT or PET/CT throughout the trial. Additionally, patients undergo bone marrow biopsy and aspiration optionally during screening and as clinically indicated on study. Patients undergo blood sample collection on study. |
Given IV
Inne nazwy:
Given IV
Inne nazwy:
Given PO
Inne nazwy:
Given IV
Inne nazwy:
Undergo ECHO
Inne nazwy:
Given IV
Inne nazwy:
Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Undergo bone marrow biopsy and aspiration Undergo bone marrow biopsy and aspiration
Inne nazwy:
Undergo radiation therapy
Inne nazwy:
Given PO
Inne nazwy:
Undergo LP
Inne nazwy:
Undergo blood and CSF sample collection
Inne nazwy:
Given SC
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Progression-free survival (PFS)
Ramy czasowe: From enrollment on the study to first occurrence of relapse/progression or death, assessed up to 7 years
|
The primary analysis will be a one-sided Log-rank test stratified by choice of backbone and radiation therapy and whether the patient had a cycle of therapy prior to enrolling. |
From enrollment on the study to first occurrence of relapse/progression or death, assessed up to 7 years
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Efficacy-related event-free survival
Ramy czasowe: Up to 7 years
|
Will be analyzed using a one-sided stratified Log-rank test at alpha = 0.05 or 0.025, as appropriate, with events defined as progression, change in therapy due to a finding that led to concern about efficacy, biopsy + disease after 6 cycles of therapy, and death. |
Up to 7 years
|
|
Therapy-related event-free survival
Ramy czasowe: Up to 7 years
|
Will be analyzed using a one-sided stratified Log-rank test at alpha = 0.05 or 0.025, as appropriate, with events defined as progression, change in therapy due to a finding that led to concern about efficacy, biopsy + disease after 6 cycles of therapy, and death. |
Up to 7 years
|
|
Overall survival
Ramy czasowe: Up to 7 years
|
Will be analyzed using a one-sided stratified Log-rank test at alpha = 0.05 or 0.025, as appropriate, with events defined as only death. |
Up to 7 years
|
|
Proportion of positive positron emission tomography (PET) scans
Ramy czasowe: Up to 6 cycle (1 cycle = 21 days)
|
Will be analyzed descriptively with a point estimate and Clopper-Pearson 95% confidence interval in the trial overall and in each treatment arm separately. The prognostic significance of positive PET after 6 cycles of therapy will be evaluated using a Cox proportional hazards regression on PFS with PET result (positive versus [vs.] negative), choice of backbone (rituximab [R]-cyclophosphamide, doxorubicin, vincristine, and prednisone [CHOP] + radiation therapy [RT] regardless of end-of-therapy imaging vs. R-CHOP without RT unless biopsy positive at end-of-therapy vs. dose-adjusted [DA]-etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin [EPOCH]-R without RT unless biopsy positive at end of therapy), and assignment to nivolumab (yes vs. no) as covariates. |
Up to 6 cycle (1 cycle = 21 days)
|
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Immune profile of patients treated with nivolumab + chemo-immunotherapy
Ramy czasowe: Up to 7 years
|
Analysis will be by paired t-test (for pre- vs. post-treatment measurements) or two-sample equal-variance t-test (for comparisons of nivolumab vs. non-nivolumab or responders [complete response/partial response] vs. non-responders [stable disease/progressive disease]). |
Up to 7 years
|
|
Complete response rate
Ramy czasowe: At the completion of initial planned therapy
|
Will be described using point estimates and Clopper-Pearson 95% confidence intervals for the complete response rate overall and in each treatment arm separately. |
At the completion of initial planned therapy
|
Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Lisa G Roth, Children's Oncology Group
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Peptydy
- Aminokwasy, peptydy i białka
- Białka
- Organiczne chemikalia
- Związki heterocykliczne
- Związki heterocykliczne, 2-ring
- Związki heterocykliczne, sterowanie stopieniem
- Techniki śledcze
- Lecznictwo
- Techniki laboratoryjne kliniczne
- Techniki i procedury diagnostyczne
- Diagnoza
- Nakłucia
- Procedury chirurgiczne, operacyjny
- Techniki cytologiczne
- Cytodiagnoza
- Węglowodory
- Węglowodory, cykliczne
- Czynniki biologiczne
- Węglowodany
- Zjawiska fizyczne
- Alkaloidy
- Policykliczne aromatyczne węglowodory
- Węglowodory, aromatyczne
- Związki policykliczne
- Glikozydy
- Hydrolazy glikozydowe
- Hydrolazy
- Enzymy
- Enzymy i koenzymy
- Polisacharyd-Lyaza
- Lyaza z tlenkiem węgla
- Lyazy
- Indole
- Przeciwciała, monoklonalne, humanizowane
- Przeciwciała, monoklonalne
- Przeciwciała
- Immunoglobuliny
- Immunoproteiny
- Białka krwi
- Globuliny w surowicy
- Globuliny
- Ciąży
- Ciężarne
- Steroidy
- Związki sterownika
- Techniki diagnostyczne, chirurgiczne
- Techniki chemii, analityczne
- Analiza widma
- Mostki fosforamidu
- Związki musztardy azotu
- Związki musztardy
- Węglowodory, uboczne
- Fosforamidy
- Związki okorosfosforowe
- Międzykomórkowe peptydy sygnalizacyjne i białka
- Ciąży
- Ciąży
- Vinca alkaloidy
- Sesologanina alkaloidy tryptaminy
- Alkaloidy indole
- Indolizicyny
- Indolizyny
- Antracykliny
- Naftaceny
- Aminoglikozydy
- Glikoproteiny
- Glikokoniugaty
- Przeciwciała, monoklonalne, mysie
- Daunorubicyna
- Techniki diagnostyczne, neurologiczne
- Czynniki stymulujące kolonię
- Czynniki wzrostu komórek hematopoetycznych
- Cytokiny
- Niwolumab
- Rytuksymab
- Prednizon
- Prednizolon
- Cyklofosfamid
- Doksorubicyna
- Winkrystyna
- Metyloprednizolon
- Radioterapia
- Hialuronoglukozaminidaza
- Promieniowanie
- Biopsja
- Prowadzenie okazów
- Spektroskopia rezonansu magnetycznego
- Kłucie kręgosłupa
- CT-P10
- Czynnik stymulujący kolonię granulocytów
- Filgrastim
- Deltacortene
- prednielidene
- Pegfilgrastim
- Fosforan etopozydowy
- Pegylowany czynnik stymulujący kolonię granulocytów
Inne numery identyfikacyjne badania
- NCI-2021-01071
- U10CA180886 (Grant/umowa NIH USA)
- NCI-2021-01071 (Identyfikator rejestru: CTRP (Clinical Trial Reporting Program))
- ANHL1931 (Inny identyfikator: CTEP)
- ANHL1931 (Inny identyfikator: Children's Oncology Group)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
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.
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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