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Testing Blinatumomab With or Without Revumenib in Patients With B-cell Acute Lymphoblastic Leukemia With a Genetic Change Requiring More Treatment

2026년 6월 3일 업데이트: SWOG Cancer Research Network

A Phase II Randomized Study of Blinatumomab With or Without Revumenib for Patients With KMT2A-Translocation B-Cell Acute Lymphoblastic Leukemia (ALL)/ Acute Leukemia With Ambiguous Lineage (ALAL) With Persistent Measurable Residual Disease (MRD)

This phase II trial tests how well adding revumenib to usual treatment (blinatumomab) compared to usual treatment alone works in treating patients with B-cell acute lymphoblastic leukemia (B-ALL) or acute leukemia with ambiguous lineage (ALAL) with KMT2A-translocation. Revumenib binds to a protein called menin and keeps it from binding to another protein called KMT2A. This stops or slows the growth of leukemia cells with changes in the KMT2A gene. Blinatumomab binds to CD19, which is found on most B cells (a type of white blood cell) and some types of leukemia cells. It also binds to a protein called CD3, which is found on T cells (another type of white blood cell). This may help the immune system kill cancer cells. In addition to blinatumomab, usual treatment also includes dexamethasone, methotrexate, cyclophosphamide, cytarabine, mercaptopurine, calaspargase pegol, doxorubicin, thioguanine, daunorubicin, vincristine and leucovorin. Dexamethasone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Methotrexate is in a class of medications called antimetabolites. It is also a type of antifolate. Methotrexate stops cells from using folic acid to make deoxyribonucleic acid (DNA) and may kill cancer cells. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's DNA and may kill cancer cells. It may also lower the body's immune response. Chemotherapy drugs, such as cytarabine, mercaptopurine, calaspargase pegol, doxorubicin, thioguanine, and daunorubicin, 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. Vincristine is in a class of medications called vinca alkaloids. It works by stopping cancer cells from growing and dividing and may kill them. Leucovorin is also being studied in the treatment of cancer. It is a type of chemoprotective agent and a type of chemosensitizing agent. Adding revumenib to usual treatment with blinatumomab may be safe, tolerable and more effective than blinatumomab alone in lowering the amount of leukemia in patients with B-ALL or ALAL with the KMT2A translocation.

연구 개요

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정황

개입 / 치료

상세 설명

PRIMARY OBJECTIVES:

I. Among participants enrolled to the safety run-in cohort, to evaluate the safety of blinatumomab with revumenib in this participant population. (Cohort A: Children [≥ 1 year] and adults with CD19-positive [CD19+] KMT2Ar B-cell acute lymphoblastic leukemia [ALL]/ acute leukemia with ambiguous lineage [ALAL] in morphological first complete remission [CR1]) II. First primary randomized objective: Among participants with positive measurable residual disease (MRD) by clonoSEQ before randomization, to compare the rates of MRD negative complete remission (CR) by clonoSEQ after the completion of one cycle of blinatumomab versus one cycle of blinatumomab plus revumenib. (Cohort A: Children [≥ 1 year] and adults with CD19-positive [CD19+] KMT2Ar B-cell acute lymphoblastic leukemia [ALL]/ acute leukemia with ambiguous lineage [ALAL] in morphological first complete remission [CR1]) III. Secondary primary randomized objective (hierarchical tested): Among participants with positive MRD by clonoSEQ before randomization, if rates of MRD negative CR by clonoSEQ after completion of one cycle of therapy are improved with blinatumomab plus revumenib versus blinatumomab, to evaluate whether MRD-event-free survival is improved among patients randomized to blinatumomab plus revumenib versus blinatumomab. (Cohort A: Children [≥ 1 year] and adults with CD19-positive [CD19+] KMT2Ar B-cell acute lymphoblastic leukemia [ALL]/ acute leukemia with ambiguous lineage [ALAL] in morphological first complete remission [CR1]) IV. To describe and evaluate the feasibility of revumenib in combination with reduced intensity multiagent chemotherapy in this participant population. (Cohort B: Untreated newly diagnosed KMT2Ar B/T-ALL or ALAL in older adults [age ≥ 55 years])

SECONDARY OBJECTIVES:

I. Within each arm and cohort and across cycles of therapy, to estimate the frequency and severity of toxicities.

II. In Cohort A: Among participants with positive MRD by clonoSEQ before randomization, to estimate the rate of MRD negative CR by clonoSEQ after two cycles of blinatumomab or blinatumomab plus revumenib.

III. In Cohort A: Among participants with negative MRD by clonoSEQ before randomization, to estimate 6-month event-free survival and MRD-event-free survival in each arm.

IV. In Cohort A: Among participants with negative MRD by clonoSEQ before randomization, to estimate 6-month event-free survival in each arm.

V. In Cohort B: To estimate the post induction composite morphological CR (CR/CR with incomplete count recovery [CRi]) rate.

VI. To estimate proportion of participants MRD negative by multi-color flow cytometry after induction (Cohort B) and cycle 1 of blinatumomab (Cohorts A + B, including the safety cohort of Cohort A).

VII. Within each arm and cohort cohort (including the safety cohort of Cohort A): To estimate the rates of lineage switch and/or CD19-negative (CD19-) relapse.

VIII. Within each arm and cohort cohort (including the safety cohort of Cohort A): To estimate the rate of allogeneic hematopoietic stem cell transplantation (HSCT) in CR1.

IX. Within each arm and cohort cohort (including the safety cohort of Cohort A): To estimate event-free survival (EFS), MRD-EFS, relapse-free survival (RFS), progression-free survival (PFS), and MRD-PFS within each arm and cohort (including the safety cohort of Cohort A) and by age ≥ 1 year to < 18 years versus ≥ 18 years of age.

X. Within each arm and cohort cohort (including the safety cohort of Cohort A): To estimate time to MRD relapse by flow cytometry and/or clonoSEQ.

XI. Within each arm and cohort cohort (including the safety cohort of Cohort A): To estimate overall survival (OS).

TRANSLATIONAL MEDICINE OBJECTIVES:

I. To estimate the frequency of MEN1 mutations by quantitative polymerase chain reaction (qPCR) and/or high sensitivity next generation sequencing (NGS) pre-induction (Cohort B), pre-randomization (Cohort A), after blinatumomab treatment (Cohorts A and B) and at the time of relapse (Cohorts A and B). (Primary) II. To estimate the rate of KMT2A fusion reverse transcriptase (RT)-PCR MRD negativity after the first and second cycle of blinatumomab therapy within treatment arms in Cohort A. (Secondary) III. To estimate the rate of KMT2A fusion RT-PCR MRD negativity after chemotherapy induction and blinatumomab post-induction therapy in Cohort B. (Secondary) V. To estimate the rate of immunoglobulin (IG)/T cell receptor (TR) variable (V) (diversity [D]) joining (J) next generation (NGS) MRD negative remission after first and second cycle of blinatumomab across treatment cohorts in Cohort A (among those with diagnosis specimens available) and after induction and blinatumomab (if administered) in Cohort B. (Secondary) V. To descriptively report changes in gene expression between diagnosis (in Cohort B, and as available in Cohort A) and relapse samples by ribonucleic acid (RNA) sequencing of registration and relapse samples. (Secondary)

OUTLINE: Patients 1 year of age or older with B-cell ALL or ALAL are assigned to Cohort A. Patients 55 and older with B-ALL, T-ALL or ALAL are assigned to Cohort B.

COHORT A: The first 6-12 eligible patients are assigned to Arm 1. Subsequent patients are randomized to Arm 1 or Arm 2.

ARM 1:

BLINATUMOMAB AND REVUMENIB CYCLE 1 (35 DAYS): Patients receive revumenib orally (PO) twice daily (BID) on days 4-28 of cycle 1, blinatumomab intravenously (IV) continuously on days 1-28 of cycle 1, dexamethasone PO or IV on days 1 and 8 (if indicated) of cycle 1, and methotrexate intrathecally (IT) on days 1 and 15 of cycle 1.

CONSOLIDATION PART 1 AND PART 2 (56 DAYS): Patients receive cyclophosphamide IV over 30-60 minutes on days 1 and 29, cytarabine IV over 1-30 minutes or subcutaneously (SC) on days 1-4, 8-11, 29-32, and 36-39, mercaptopurine PO once daily (QD) on days 1-14 and 29-42, methotrexate IT on days 1, 8, 15, and 22 or on days 1, 8, 29, and 43, vincristine IV on days 15, 22, 43, and 50 and calaspargase pegol IV over 1-2 hours on days 15 and 43 in the absence of disease progression or unacceptable toxicity.

BLINATUMOMAB AND REVUMENIB CYCLE 2 (35 DAYS): Patients receive revumenib PO BID on days 1-28 of cycle 2, blinatumomab IV continuously on days 1-28 of cycle 2, dexamethasone PO or IV on day 1 of cycle 2, and methotrexate IT on days 1 and 15 of cycle 2.

INTERIM MAINTENANCE 1 (63 DAYS): Patients receive vincristine IV on days 1, 15, 29, and 43, high dose methotrexate IV over 24 hours on days 1, 15, 29, and 43, leucovorin PO or IV on days 3-4, 17-18, 31-32, and 45-46, mercaptopurine PO on days 1-14, 15-28, 29-42, and 43-56, and methotrexate IT on days 1 and 29 in the absence of disease progression or unacceptable toxicity.

DELAYED INTENSIFICATION PART 1 AND PART 2 (63 DAYS): Patients receive methotrexate IT on days 1, 29, and 36, dexamethasone PO BID or IV on days 1-7 and 15-21, vincristine IV on days 1, 8, 15, 43, and 50, doxorubicin IV over 3-15 minutes on days 1, 8, and 15, calaspargase pegol IV over 1-2 hours on days 4 and 43, cyclophosphamide IV over 30-60 minutes on day 29, thioguanine PO on days 29-42 and cytarabine IV over 1-30 minutes or SC on days 29-32 and 36-39 in the absence of disease progression or unacceptable toxicity.

INTERIM MAINTENANCE 2 (56 DAYS): Patients receive vincristine IV on days 1, 11, 21, 31, and 41, methotrexate IV on days 1, 11, 21, 31, and 41, methotrexate IT on days 1 and 31 and calaspargase pegol IV over 1-2 hours on days 2 and 23 in the absence of disease progression or unacceptable toxicity.

Additionally, patients undergo chest x-ray and echocardiography (ECHO) or multigated acquisition scan (MUGA) at screening and bone marrow biopsy and aspiration, cerebrospinal fluid (CSF) and blood sample collection, computed tomography (CT) or positron emission tomography (PET)/CT throughout the study.

ARM 2:

BLINATUMOMAB CYCLE 1 (35 DAYS): Patients blinatumomab IV continuously on days 1-28 of cycle 1, dexamethasone PO or IV on days 1 and 8 (if indicated) of cycle 1, and methotrexate IT on days 1 and 15 of cycle 1.

CONSOLIDATION PART 1 AND PART 2 (56 DAYS): Patients receive cyclophosphamide IV over 30-60 minutes on days 1 and 29, cytarabine IV over 1-30 minutes or SC on days 1-4, 8-11, 29-32, and 36-39, mercaptopurine PO QD on days 1-14 and 29-42, methotrexate IT on days 1, 8, 15, and 22 or on days 1, 8, 29, and 43, vincristine IV on days 15, 22, 43, and 50 and calaspargase pegol IV over 1-2 hours on days 15 and 43 in the absence of disease progression or unacceptable toxicity.

BLINATUMOMAB CYCLE 2 (35 DAYS): Patients receive blinatumomab IV continuously on days 1-28 of cycle 2, dexamethasone PO or IV on day 1 of cycle 2, and methotrexate IT on days 1 and 15 of cycle 2.

INTERIM MAINTENANCE 1 (63 DAYS): Patients receive vincristine IV on days 1, 15, 29, and 43, high dose methotrexate IV over 24 hours on days 1, 15, 29, and 43, leucovorin PO or IV on days 3-4, 17-18, 31-32, and 45-46, mercaptopurine PO on days 1-14, 15-28, 29-42, and 43-56, and methotrexate IT on days 1 and 29 in the absence of disease progression or unacceptable toxicity.

DELAYED INTENSIFICATION PART 1 AND PART 2 (63 DAYS): Patients receive methotrexate IT on days 1, 29, and 36, dexamethasone PO BID or IV on days 1-7 and 15-21, vincristine IV on days 1, 8, 15, 43, and 50, doxorubicin IV over 3-15 minutes on days 1, 8, and 15, calaspargase pegol IV over 1-2 hours on days 4 and 43, cyclophosphamide IV over 30-60 minutes on day 29, thioguanine PO on days 29-42, and cytarabine IV over 1-30 minutes or SC on days 29-32 and 36-39 in the absence of disease progression or unacceptable toxicity.

INTERIM MAINTENANCE 2 (56 DAYS): Patients receive vincristine IV on days 1, 11, 21, 31, and 41, methotrexate IV on days 1, 11, 21, 31, and 41, methotrexate IT on days 1 and 31 and calaspargase pegol IV over 1-2 hours on days 2 and 23 in the absence of disease progression or unacceptable toxicity.

Additionally, patients undergo chest x-ray and ECHO or MUGA at screening and bone marrow biopsy and aspiration, CSF and blood sample collection, CT or PET/CT throughout the study.

COHORT B:

INDUCTION (35 DAYS): Patients receive cytarabine IT on day 1 of cycle 1, vincristine IV on days 1, 8, 15, and 22 of cycle 1, dexamethasone PO or IV BID on days 1-7 and 15-21 or IV BID on days 1-7 of cycle 1, daunorubicin IV on days 1, 8, and 15 of cycle 1, methotrexate IT on days 8 and 29 or once weekly of cycle 1, and revumenib PO BID on days 8-28 of cycle 1.

POST-INDUCTION (84 DAYS): Patients with morphological CR after induction treatment may receive revumenib PO BID on days 4-28 of cycle 1 and on days 1-28 of cycle 2, blinatumomab IV continuously on days 1-28 of cycles 1 and 2 and methotrexate IT on days 1 and 15 of cycles 1 and 2. Cycles repeat every 42 days for up to 2 cycles in the absence of disease progression or unacceptable toxicity.

Additionally, patients undergo bone marrow biopsy and aspiration, CSF and blood sample collection, CT or PET/CT throughout the study.

After completion of study treatment, patients are followed every 3 months for the first 2 years, every 6 months for years 3-5 and then annually for up to 10 years after registration.

연구 유형

중재적

등록 (추정된)

90

단계

  • 2 단계

참여기준

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설명

Inclusion Criteria:

  • COHORT A: Participants must meet diagnostic criteria for either B-cell acute lymphoblastic leukemia (ALL) with KMT2A-translocation or acute leukemia with ambiguous lineage (ALAL) with KMT2A-translocation
  • COHORT A: Participants must have KMT2A-translocation documented locally by conventional cytogenetics, fluorescence in situ hybridization (FISH) or molecular studies such as next generation sequencing (NGS)
  • COHORT A: Participants must have achieved morphological first complete remission (CR1) after induction cycle (s) as defined bone marrow lymphoblasts < 5%

  • COHORT A: Participants must have either known trackable clone(s) by clonoSEQ that was identified at initial diagnosis, or a banked diagnostic sample, which can include clinical samples from the treating institution, available that can be used to identify trackable clone(s)

    • Participants must not be known not to have trackable clones by clonoSEQ
    • Participants must not be known already to have MRD-negativity by clonoSEQ prior to enrollment
  • COHORT A: Participants must have evidence of CD19 expression at any level in ALL or ALAL documented locally by flow cytometry or immunohistochemistry in bone marrow or peripheral blood at the time of initial diagnosis. Immunophenotyping of the blood or marrow lymphoblasts must be performed to determine lineage. Appropriate marker studies including CD19 (B cell) must be performed. If a bone marrow aspirate cannot be obtained despite an attempt (dry tap), appropriate Immunohistochemistry (IHC) testing, including CD19, must be performed on the bone marrow biopsy to determine lineage
  • COHORT A: Participants must have Philadelphia-chromosome negative ALL or ALAL
  • COHORT A: Participants must not have known lymphoid blast crisis arising from chronic myeloid leukemia (CML) or have received previous tyrosine kinase inhibitor (TKI) therapy for their chronic myeloid leukemia (CML)

  • COHORT B: Participants must meet diagnostic criteria for either newly diagnosed with acute lymphoblastic leukemia (ALL) or acute leukemia with ambiguous lineage (ALAL)

    • Participants with either B or T-cell subtypes of ALL are permitted on Cohort B
    • Participants must have KMT2A-translocation documented locally by conventional cytogenetics, fluorescence in situ hybridization (FISH) or molecular studies such as next generation sequencing (NGS)
  • COHORT B: Participants must have Philadelphia-chromosome negative ALL or ALAL
  • COHORT B: Participants must not have known lymphoid blast crisis arising from CML or have received previous TKI therapy for their chronic myeloid leukemia (CML)
  • COHORT A: Participants ≥ 18 years may have received 1 to 3 cycles of induction/consolidation before entering the study. It is encouraged to enroll participants immediately after completing the first induction cycle if the patient achieves morphological CR. For pediatric patients < 18 years of age, enrollment must occur after induction therapy
  • COHORT A: Participants must discontinue strong cytochrome P450 (CYP)3A4 inhibitors or strong or moderate inducers, except corticosteroids, within 14 days prior to registration

  • COHORT A: Participants must have recovered from any prior major surgery adverse effects at least 14 days prior to registration, to the satisfaction of the local investigator

    • Note: Central venous access placement is not considered major surgery for the purposes of this protocol
  • COHORT A: Participants must not be receiving any oral or intravenous systemic immunosuppressive therapy with the exception of induction/consolidation chemotherapy for the treatment of their current ALL or ALAL. Participants may receive up to 10 mg per day of prednisone or prednisone equivalent for adrenal insufficiency or other indications
  • COHORT A: Participants must not have received a prior allogeneic hematopoietic stem cell transplant
  • COHORT A: Participants must not have received prior blinatumomab, menin inhibitors, chimeric antigen receptor (CAR)-T therapy, or anti-CD19 antibodies

  • COHORT B: Participants must not have received prior systemic therapy for ALL or ALAL, with the exception of hydroxyurea, steroid, retinoic acid, intrathecal chemotherapy, or induction chemotherapy as defined below

    • Participants who have been started on the study regimen backbone (i.e. induction therapy) before consenting and then are found to have the KMT2Ar and are eligible for the study, can be enrolled on the study as long as revumenib treatment can be started by day 8 of induction therapy
  • COHORT B: Participants must discontinue strong CYP3A4 inhibitors or strong or moderate inducers, except corticosteroids, within 14 days prior to registration

  • COHORT B: Participants must have recovered from any prior major surgery adverse effects at least 14 days prior to registration, to the satisfaction of the local investigator

    • Note: Central venous access placement is not considered major surgery for the purposes of this protocol
  • COHORT B: Participants must not be receiving any systemic oral or intravenous immunosuppressive therapy with the exception of induction chemotherapy or corticosteroid for the treatment of their current ALL or ALAL
  • COHORT B: Participants must not have received a prior allogeneic hematopoietic stem cell transplant
  • COHORT A: Participant must be ≥ 1 years old at the time of registration. There is no upper age limit
  • COHORT A: Participant must have Zubrod/Eastern Cooperative Oncology Group (ECOG) performance status of 0-2, or Lansky/Karnofsky performance status scores of 50-100
  • COHORT A: Participants must have a complete medical history and physical exam within 28 days prior to registration
  • COHORT A: Glomerular filtration rate (GFR) ≥ 50 ml/min/1.73 m^2 (within 14 days prior to registration)
  • COHORT A: Absolute neutrophil count ≥ 1 x 10^3/uL (within 14 days prior to registration)
  • COHORT A: Platelets ≥ 100 x 10^3/uL (within 14 days prior to registration)

  • COHORT A: Direct bilirubin ≤ 2.0 mg/dL (34.2 micromoles/L) (within 14 days prior to registration)

    • Note: Participants with history of Gilbert's disease must have direct bilirubin ≤ 5 x institutional upper limit of normal (ULN)
  • COHORT A: Alanine aminotransferase (ALT) ≤ 5 x institutional ULN (within 14 days prior to registration)
  • COHORT A: Participants ≥ 18 years must have a calculated creatinine clearance ≥ 50 mL/min using the following Cockcroft-Gault formula. This specimen must have been drawn and processed within 14 days prior to registration

  • COHORT A: Adequate renal function for participants < 18 years of age is defined as:

    • A GFR ≥ 50 mL/min/1.73 m^2, as determined by one of the following methods:

      • Estimated GFR (eGFR) ≥ 50 mL/min/1.73 m^2 "Bedside" Schwartz formula (2009)
      • 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)
  • COHORT A: Participants must have adequate cardiac function. Participants must have cardiac ejection fraction ≥ 50% by MUGA or 2 dimensional (2-D) echocardiogram or shortening fraction (SF) ≥ 27% by echocardiogram within 90 days prior to registration. Participants with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, must have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, participants must be class 2B or better
  • COHORT A: Participants ≥ 18 years of age with a known history of human immunodeficiency virus (HIV)-infection must be on effective anti-retroviral therapy at registration and have undetectable viral load test on the most recent test results obtained within 6 months prior to registration
  • COHORT A: Participants ≥ 18 years of age with a known history of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load while on suppressive therapy on the most recent test results obtained within 6 months prior to registration, if indicated
  • COHORT A: Participants ≥ 18 years of age with a known history of hepatitis C virus (HCV) infection must have been treated and cured. Participants currently being treated for HCV infection must have undetectable HCV viral load test on the most recent test results obtained within 6 months prior to registration, if indicated
  • COHORT A: Participants must not have prolonged Fridericia's formula-corrected QT interval (QTcf) defined as > 450 msec on screening electrocardiogram (EKG) prior to registration
  • COHORT A: Participants must not have relapsed or refractory disease in the bone marrow (≥ 5% blasts) or extramedullary sites involvement
  • COHORT A: Participants must not have systemic fungal, bacterial, viral or other infection that is not controlled (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment) as determined by the local investigator
  • COHORT A: Participants must not have clinically significant autoimmune disease
  • COHORT A: Participants must be able to take oral medications and comply with the oral regimen Participants must be able to swallow and retain oral medications and have no known gastrointestinal disorders likely to interfere with absorption of oral medications. Administration via nasogastric/gastrostomy (NG/G)-tube is acceptable as long as oral solution is used

  • COHORT A: Participants must not have uncontrolled intercurrent illness including, but not limited to:

    • Active central nervous system status 3 (CNS3) or CNS2 (CNS leukemia)

      • Note: Participants with CNS1 or who had prior CNS2 or CNS3 are eligible if this has cleared and have become CNS-1
    • Currently requiring supplemental oxygen (more than 2 liters per minute), mechanical ventilation, vasopressors
  • COHORT A: Participants must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the investigational regimen

  • COHORT A: Participants must not be pregnant or nursing. Individuals who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has had menses at any time in the preceding 24 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen

    • Note: Participants of childbearing potential must have a negative pregnancy test within 7 days prior to starting treatment
  • COHORT B: Participant must be ≥ 55 years old at the time of registration
  • COHORT B: Participant must have Zubrod/ECOG performance status of 0-2
  • COHORT B: Participants must have a complete medical history and physical exam within 28 days prior to registration
  • COHORT B: GFR ≥ 50 ml/min/1.73 m^2 (within 14 days prior to registration)

  • COHORT B: Direct bilirubin ≤ 2.0 mg/dL (34.2 micromoles/L) (within 14 days prior to registration)

    • Note: Participants with history of Gilbert's disease or elevated bilirubin is related to underlying leukemia must have direct bilirubin ≤ 5 x institutional ULN
  • COHORT B: ALT ≤ 5 x institutional ULN unless abnormal liver tests are related to underlying leukemia (within 14 days prior to registration)
  • COHORT B: Participants must have a calculated creatinine clearance ≥ 50 mL/min using the following Cockcroft-Gault formula. This specimen must have been drawn and processed within 14 days prior to registration
  • COHORT B: Participants must have adequate cardiac function. Participants must have cardiac ejection fraction ≥ 50% by MUGA or 2-D echocardiogram within 28 days prior to registration. Participants with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, must have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, participants must be class 2B or better
  • COHORT B: Participants with a known history human immunodeficiency virus (HIV)-infection must be on effective anti-retroviral therapy at registration and have undetectable viral load test on the most recent test results obtained within 6 months prior to registration
  • COHORT B: Participants with a known history of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load while on suppressive therapy on the most recent test results obtained within 6 months prior to registration, if indicated
  • COHORT B: Participants with a known history of hepatitis C virus (HCV) infection must have been treated and cured. Participants currently being treated for HCV infection must have undetectable HCV viral load test on the most recent test results obtained within 6 months prior to registration, if indicated
  • COHORT B: Participants must have a lumbar puncture to determine CNS involvement of ALL within 14 days prior to registration. Intrathecal cytarabine and/or methotrexate administered prior to study registration may count as the first dose of intrathecal therapy required as part of protocol therapy
  • COHORT B: Participants must not have an active uncontrolled infection
  • COHORT B: Participants must not have prolonged QTcf defined as > 450 msec participants on screening EKG prior to registration
  • COHORT B: Participants must not have known clinical signs of bulk central nervous system involvement (CNS3c), such as facial palsy, brain/eye involvement or hypothalamic syndrome
  • COHORT B: Participants must be able to take oral medications and comply with the oral regimen Participants must be able to swallow and retain oral medications and have no known gastrointestinal disorders likely to interfere with absorption of oral medications. Administration via NG/G-tube is acceptable as long as oral solution is used
  • COHORT B: Participants must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the investigational regimen

  • COHORT B: Participants must not be pregnant or nursing. Individuals who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has had menses at any time in the preceding 24 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen

    • Note: Participants of childbearing potential must have a negative pregnancy test within 7 days prior to starting treatment
  • ALL COHORTS: Participants must be offered the opportunity to participate in specimen collection submitted for translational medicine work. With participant consent, specimens must be collected and submitted via the Southwest Oncology Group (SWOG) Specimen Tracking System

  • NOTE: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system

    • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines
    • For participants with impaired decision-making capabilities, legally authorized representatives may sign and give informed consent on behalf of study participants in accordance with applicable federal, local, and Central Institutional Review Board (CIRB) regulations
    • This trial will use a slot reservation system to enroll the feasibility and safety run-in portions of the study for Cohort A and Cohort B. Patients planning to enroll at this portion of the study must first have a slot reserved in advance of the registration. All site staff will use OPEN to create a slot reservation

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무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Cohort A, Arm 1 (revumenib and blinatumomab)
See Detailed Description.
의약품: 사이클로포스파마이드
주어진 IV
다른 이름들:
  • 사이톡산
  • CTX
  • (-)-시클로포스파미드
  • 2H-1,3,2-옥사자포스포린, 2-[비스(2-클로로에틸)아미노]테트라하이드로-, 2-옥사이드, 일수화물
  • 칼록산
  • 시클로포스파미다
  • 시클로포스파마이드
  • 시클록살
  • 클라펜
  • CP 일수화물
  • CYCLO 셀
  • 사이클로블라스틴
  • 사이클로포스팜
  • 사이클로포스파미드 일수화물
  • 사이클로포스파미둠
  • 시클로포스판
  • 사이클로포스판
  • 시클로포스파늄
  • 사이클로스틴
  • 사이토포스판
  • 포스파세론
  • 제녹살
  • 제눅살
  • 레독시나
  • 미톡산
  • 네오사르
  • 리바이뮨
  • 실클로포스파미드
  • WR-138719
  • 아스타 B 518
  • B-518
  • B518
  • WR 138719
  • WR138719
의약품: 메르캅토퓨린
주어진 PO
다른 이름들:
  • 6MP
  • 퓨리네톨
  • 3H-퓨린-6-티올
  • 6 티오히폭산틴
  • 6 티오퓨린
  • 6-메르캅토퓨린
  • 6-메르캅토퓨린 일수화물
  • 6-푸리네티올
  • 6-티오퓨린
  • 6-티옥소퓨린
  • 6H-퓨린-6-티온, 1,7-디하이드로-(9CI)
  • 7-메르캅토-1,3,4,6-테트라자인덴
  • 알티-메르캅토퓨린
  • 아자티오퓨린
  • Bw 57-323H
  • 플로코필
  • 이스미푸르
  • 류케린
  • 류푸린
  • 메르카루킴
  • 머칼루킨
  • 메르캅티나
  • 메르캅토푸리눔
  • 메르카푸린
  • 머른
  • NCI-C04886
  • 푸리-네트톨
  • 퓨리메톨
  • 퓨린, 6-메르캅토-
  • 퓨린-6-티올(8CI)
  • 퓨린-6-티올, 일수화물
  • 퓨리네티올
  • U-4748
  • WR-2785
의약품: 덱사메타손
주어진 PO 또는 IV
다른 이름들:
  • 데카드론
  • 헤마디
  • Aacidexam
  • 아덱손
  • 아크니히톨 덱사
  • 알바덱스
  • 알린
  • 알린 디포
  • 알린 오프탈미코
  • 증폭
  • 안물모노
  • 오리쿨라룸
  • 옥실로손
  • 베이카드론
  • 바이큐텐
  • 베이큐튼 N
  • 코르티덱사손
  • 코르티섬만
  • 데카코트
  • 데카드롤
  • 데카드론 DP
  • 데칼릭스
  • 데카메스
  • 데카손 R.p.
  • 데탄실
  • 델타플루오렌
  • 데로닐
  • 데사메타손
  • 데사메톤
  • 덱사-마말렛
  • 덱사-코뿔소
  • 덱사-스케로손
  • 덱사 사인
  • 덱사피질
  • 덱사코르틴
  • 덱사파마
  • 덱사플루오렌
  • 덱사로컬
  • 덱사메코르틴
  • 덱사메스
  • 덱사메타손 인텐솔
  • 덱사메타소눔
  • 덱사모노존
  • 덱사포스
  • 덱시노랄
  • 덱손
  • 다이노르몬
  • 드제보
  • 플루오로델타
  • 포르테코틴
  • 감마코르텐
  • 헥사데카드롤
  • 헥사드롤
  • 로컬리슨-F
  • 로베린
  • 메틸플루오르프레드니솔론
  • 밀리코트
  • 마이메타손
  • 오르가드론
  • 스퍼사덱스
  • 테이퍼덱스
  • 비스메타존
  • 조덱스
  • 레나덱스
의약품: 빈크리스틴
주어진 IV
다른 이름들:
  • VCR
  • 류로크리스틴
  • 빈크리스틴
  • LCR
생물학적: 블리나투모맙
주어진 IV
다른 이름들:
  • 블린사이토
  • 항-CD19 x 항-CD3 이중특이성 단클론항체
  • 항-CD19/항-CD3 재조합 이중특이성 단클론 항체 MT103
  • 메디-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
  • 메디 538
  • MT 103
의약품: 티오구아닌
주어진 PO
다른 이름들:
  • 6-TG
  • 2-아미노 6MP
  • 2-아미노-1,7-디하이드로-6H-퓨린-6-티온
  • 2-아미노-6-머캅토퓨린
  • 2-아미노-6-퓨리네티올
  • 2-아미노푸린-6-티올
  • 2-아미노퓨린-6(1H)-티온
  • 2-아미노퓨린-6-티올
  • 2-아미노퓨린-6-티올 반수화물
  • 2-메르캅토-6-아미노퓨린
  • 6-아미노-2-메르캅토퓨린
  • 6-메르캅토-2-아미노퓨린
  • 6-메르캅토구아닌
  • 6H-퓨린-6-티온, 2-아미노-1,7-디하이드로-(9CI)
  • BW 5071
  • 랑비스
  • 정제
  • 티오구아닌 반수화물
  • 티오구아닌 수화물
  • 티오구아닌
  • 웰컴 U3B
  • WR-1141
  • × 27
의약품: 독소루비신
주어진 IV
다른 이름들:
  • 아드리아블라스틴
  • 하이드록시다우노마이신
  • 하이드록실 다우노루비신
  • 하이드록실다우노루비신
절차: 다중 게이트 획득 스캔
무가를 겪다
다른 이름들:
  • 혈액 풀 스캔
  • 평형 방사성핵종 혈관조영술
  • 게이티드 혈액 풀 이미징
  • 무가
  • 방사성핵종 뇌실조영술
  • RNVG
  • SYMA 스캐닝
  • 동기화된 다중 게이트 수집 스캐닝
  • 무가 스캔
  • 다중 게이트 획득 스캔
  • 방사성핵종 뇌실도 스캔
  • 게이트 하트 풀 스캔
  • RNV 스캔
절차: 양전자 방출 단층 촬영
PET/CT를 받다
다른 이름들:
  • 의료 영상, 양전자 방출 단층 촬영
  • 애완 동물
  • PET 스캔
  • 양전자 방출 단층 촬영 스캔
  • 양전자 방출 단층 촬영
  • PT
  • 양전자방출단층촬영(시술)
의약품: 류코보린 칼슘
주어진 PO 또는 IV
다른 이름들:
  • 웰코보린
  • 엽산
  • 아디네파르
  • 칼시폴린
  • 칼슘(6S)-엽산
  • 칼슘 폴리네이트
  • 칼슘 류코보린
  • 칼포렉스
  • 칼리낫
  • 세하폴린
  • 시토폴린
  • 시트렉
  • 시트로보룸 팩터
  • 크로마톤빅 폴리니코
  • 달리솔
  • 디인톡스
  • 디비칼
  • 에코폴
  • 이모비스
  • 팩터, 시트로보룸
  • 플라이노켄 A
  • 폴라렌
  • 폴락신
  • FOLI 세포
  • 폴리벤
  • 폴리단
  • Folidar
  • 폴리낙
  • 엽산칼슘
  • 엽산칼슘염 5수화물
  • 폴리노랄
  • 폴린비트
  • 폴리플러스
  • 폴릭스
  • 이모
  • 레더폴랏
  • 레더폴린
  • 루코사르
  • 류코보린
  • 레스큐폴린
  • 레스큐볼린
  • 토노폴린
절차: 흉부 방사선 촬영
흉부 엑스레이를 찍다
다른 이름들:
  • 흉부 엑스레이
절차: 골수 생검
골수 생검 및 흡인
다른 이름들:
  • 골수 생검
  • 생검, 골수
의약품: 메토트렉세이트
주어진 IT 또는 IV
다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
의약품: 시타라빈
주어진 IV 또는 SC
다른 이름들:
  • .베타.-시토신 아라비노사이드
  • 1-.베타.-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-.beta.-D-Arabinofuranosylcytosine
  • 1-베타-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-베타-D-아라비노푸라노실시토신
  • 1.베타.-D-아라비노푸라노실시토신
  • 2(1H)-피리미디논, 4-아미노-1-베타-D-아라비노푸라노실-
  • 2(1H)-피리미디논, 4-아미노-1.베타.-D-아라비노푸라노실-
  • 알렉산
  • 아라씨
  • ARA 세포
  • 아라빈
  • 아라비노푸라노실시토신
  • 아라비노실시토신
  • 아라시티딘
  • 아라시티틴
  • 베타-시토신 아라비노사이드
  • CHX-3311
  • 시타라비눔
  • 시타벨
  • 사이토사르
  • 시토신 아라비노사이드
  • 시토신-.베타.-아라비노사이드
  • 시토신-베타-아라비노사이드
  • 에르팔파
  • 스타라시드
  • 타라빈 PFS
  • 유 19920
  • U-19920
  • 우디실
  • WR-28453
절차: 컴퓨터 단층 촬영
CT 또는 PET/CT를 받다
다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
의약품: 칼라스파가제 페골
주어진 IV
다른 이름들:
  • Asparaginase (Escherichia coli Isoenzyme II), alpha-(((2,5-Dioxo-1-pyrrolidinyl)oxy)carbonyl)-omega-methoxypoly(oxy-1,2-ethanediyl)과 결합
  • 아스파라스
  • EZN-2285
  • SC-PEG 대장균 L-아스파라기나제
  • 석신이미딜 카보네이트 모노메톡시폴리에틸렌 글리콜 대장균 L-아스파라기나제
  • Calaspargase Pegol-mknl
절차: 생물 표본 수집
CSF 및 혈액 샘플 채취
다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
의약품: 레부메닙
주어진 PO
다른 이름들:
  • 메닌-혼합 계통 백혈병 단백질-단백질 상호작용 억제제 SNDX-5613
  • Menin-MLL 억제제 SNDX-5613
  • Menin-MLL 상호작용 억제제 SNDX-5613
  • SNDX 5613
  • SNDX-5613
  • SNDX5613
절차: 골수 흡인
골수 생검 및 흡인
절차: 심 초음파 검사
에코를받습니다
다른 이름들:
  • 심초음파
  • EC
활성 비교기: Cohort A, Arm 2 (blinatumomab)
See Detailed Description.
의약품: 사이클로포스파마이드
주어진 IV
다른 이름들:
  • 사이톡산
  • CTX
  • (-)-시클로포스파미드
  • 2H-1,3,2-옥사자포스포린, 2-[비스(2-클로로에틸)아미노]테트라하이드로-, 2-옥사이드, 일수화물
  • 칼록산
  • 시클로포스파미다
  • 시클로포스파마이드
  • 시클록살
  • 클라펜
  • CP 일수화물
  • CYCLO 셀
  • 사이클로블라스틴
  • 사이클로포스팜
  • 사이클로포스파미드 일수화물
  • 사이클로포스파미둠
  • 시클로포스판
  • 사이클로포스판
  • 시클로포스파늄
  • 사이클로스틴
  • 사이토포스판
  • 포스파세론
  • 제녹살
  • 제눅살
  • 레독시나
  • 미톡산
  • 네오사르
  • 리바이뮨
  • 실클로포스파미드
  • WR-138719
  • 아스타 B 518
  • B-518
  • B518
  • WR 138719
  • WR138719
의약품: 메르캅토퓨린
주어진 PO
다른 이름들:
  • 6MP
  • 퓨리네톨
  • 3H-퓨린-6-티올
  • 6 티오히폭산틴
  • 6 티오퓨린
  • 6-메르캅토퓨린
  • 6-메르캅토퓨린 일수화물
  • 6-푸리네티올
  • 6-티오퓨린
  • 6-티옥소퓨린
  • 6H-퓨린-6-티온, 1,7-디하이드로-(9CI)
  • 7-메르캅토-1,3,4,6-테트라자인덴
  • 알티-메르캅토퓨린
  • 아자티오퓨린
  • Bw 57-323H
  • 플로코필
  • 이스미푸르
  • 류케린
  • 류푸린
  • 메르카루킴
  • 머칼루킨
  • 메르캅티나
  • 메르캅토푸리눔
  • 메르카푸린
  • 머른
  • NCI-C04886
  • 푸리-네트톨
  • 퓨리메톨
  • 퓨린, 6-메르캅토-
  • 퓨린-6-티올(8CI)
  • 퓨린-6-티올, 일수화물
  • 퓨리네티올
  • U-4748
  • WR-2785
의약품: 덱사메타손
주어진 PO 또는 IV
다른 이름들:
  • 데카드론
  • 헤마디
  • Aacidexam
  • 아덱손
  • 아크니히톨 덱사
  • 알바덱스
  • 알린
  • 알린 디포
  • 알린 오프탈미코
  • 증폭
  • 안물모노
  • 오리쿨라룸
  • 옥실로손
  • 베이카드론
  • 바이큐텐
  • 베이큐튼 N
  • 코르티덱사손
  • 코르티섬만
  • 데카코트
  • 데카드롤
  • 데카드론 DP
  • 데칼릭스
  • 데카메스
  • 데카손 R.p.
  • 데탄실
  • 델타플루오렌
  • 데로닐
  • 데사메타손
  • 데사메톤
  • 덱사-마말렛
  • 덱사-코뿔소
  • 덱사-스케로손
  • 덱사 사인
  • 덱사피질
  • 덱사코르틴
  • 덱사파마
  • 덱사플루오렌
  • 덱사로컬
  • 덱사메코르틴
  • 덱사메스
  • 덱사메타손 인텐솔
  • 덱사메타소눔
  • 덱사모노존
  • 덱사포스
  • 덱시노랄
  • 덱손
  • 다이노르몬
  • 드제보
  • 플루오로델타
  • 포르테코틴
  • 감마코르텐
  • 헥사데카드롤
  • 헥사드롤
  • 로컬리슨-F
  • 로베린
  • 메틸플루오르프레드니솔론
  • 밀리코트
  • 마이메타손
  • 오르가드론
  • 스퍼사덱스
  • 테이퍼덱스
  • 비스메타존
  • 조덱스
  • 레나덱스
의약품: 빈크리스틴
주어진 IV
다른 이름들:
  • VCR
  • 류로크리스틴
  • 빈크리스틴
  • LCR
생물학적: 블리나투모맙
주어진 IV
다른 이름들:
  • 블린사이토
  • 항-CD19 x 항-CD3 이중특이성 단클론항체
  • 항-CD19/항-CD3 재조합 이중특이성 단클론 항체 MT103
  • 메디-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
  • 메디 538
  • MT 103
의약품: 티오구아닌
주어진 PO
다른 이름들:
  • 6-TG
  • 2-아미노 6MP
  • 2-아미노-1,7-디하이드로-6H-퓨린-6-티온
  • 2-아미노-6-머캅토퓨린
  • 2-아미노-6-퓨리네티올
  • 2-아미노푸린-6-티올
  • 2-아미노퓨린-6(1H)-티온
  • 2-아미노퓨린-6-티올
  • 2-아미노퓨린-6-티올 반수화물
  • 2-메르캅토-6-아미노퓨린
  • 6-아미노-2-메르캅토퓨린
  • 6-메르캅토-2-아미노퓨린
  • 6-메르캅토구아닌
  • 6H-퓨린-6-티온, 2-아미노-1,7-디하이드로-(9CI)
  • BW 5071
  • 랑비스
  • 정제
  • 티오구아닌 반수화물
  • 티오구아닌 수화물
  • 티오구아닌
  • 웰컴 U3B
  • WR-1141
  • × 27
의약품: 독소루비신
주어진 IV
다른 이름들:
  • 아드리아블라스틴
  • 하이드록시다우노마이신
  • 하이드록실 다우노루비신
  • 하이드록실다우노루비신
절차: 다중 게이트 획득 스캔
무가를 겪다
다른 이름들:
  • 혈액 풀 스캔
  • 평형 방사성핵종 혈관조영술
  • 게이티드 혈액 풀 이미징
  • 무가
  • 방사성핵종 뇌실조영술
  • RNVG
  • SYMA 스캐닝
  • 동기화된 다중 게이트 수집 스캐닝
  • 무가 스캔
  • 다중 게이트 획득 스캔
  • 방사성핵종 뇌실도 스캔
  • 게이트 하트 풀 스캔
  • RNV 스캔
절차: 양전자 방출 단층 촬영
PET/CT를 받다
다른 이름들:
  • 의료 영상, 양전자 방출 단층 촬영
  • 애완 동물
  • PET 스캔
  • 양전자 방출 단층 촬영 스캔
  • 양전자 방출 단층 촬영
  • PT
  • 양전자방출단층촬영(시술)
의약품: 류코보린 칼슘
주어진 PO 또는 IV
다른 이름들:
  • 웰코보린
  • 엽산
  • 아디네파르
  • 칼시폴린
  • 칼슘(6S)-엽산
  • 칼슘 폴리네이트
  • 칼슘 류코보린
  • 칼포렉스
  • 칼리낫
  • 세하폴린
  • 시토폴린
  • 시트렉
  • 시트로보룸 팩터
  • 크로마톤빅 폴리니코
  • 달리솔
  • 디인톡스
  • 디비칼
  • 에코폴
  • 이모비스
  • 팩터, 시트로보룸
  • 플라이노켄 A
  • 폴라렌
  • 폴락신
  • FOLI 세포
  • 폴리벤
  • 폴리단
  • Folidar
  • 폴리낙
  • 엽산칼슘
  • 엽산칼슘염 5수화물
  • 폴리노랄
  • 폴린비트
  • 폴리플러스
  • 폴릭스
  • 이모
  • 레더폴랏
  • 레더폴린
  • 루코사르
  • 류코보린
  • 레스큐폴린
  • 레스큐볼린
  • 토노폴린
절차: 흉부 방사선 촬영
흉부 엑스레이를 찍다
다른 이름들:
  • 흉부 엑스레이
절차: 골수 생검
골수 생검 및 흡인
다른 이름들:
  • 골수 생검
  • 생검, 골수
의약품: 메토트렉세이트
주어진 IT 또는 IV
다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
의약품: 시타라빈
주어진 IV 또는 SC
다른 이름들:
  • .베타.-시토신 아라비노사이드
  • 1-.베타.-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-.beta.-D-Arabinofuranosylcytosine
  • 1-베타-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-베타-D-아라비노푸라노실시토신
  • 1.베타.-D-아라비노푸라노실시토신
  • 2(1H)-피리미디논, 4-아미노-1-베타-D-아라비노푸라노실-
  • 2(1H)-피리미디논, 4-아미노-1.베타.-D-아라비노푸라노실-
  • 알렉산
  • 아라씨
  • ARA 세포
  • 아라빈
  • 아라비노푸라노실시토신
  • 아라비노실시토신
  • 아라시티딘
  • 아라시티틴
  • 베타-시토신 아라비노사이드
  • CHX-3311
  • 시타라비눔
  • 시타벨
  • 사이토사르
  • 시토신 아라비노사이드
  • 시토신-.베타.-아라비노사이드
  • 시토신-베타-아라비노사이드
  • 에르팔파
  • 스타라시드
  • 타라빈 PFS
  • 유 19920
  • U-19920
  • 우디실
  • WR-28453
절차: 컴퓨터 단층 촬영
CT 또는 PET/CT를 받다
다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
의약품: 칼라스파가제 페골
주어진 IV
다른 이름들:
  • Asparaginase (Escherichia coli Isoenzyme II), alpha-(((2,5-Dioxo-1-pyrrolidinyl)oxy)carbonyl)-omega-methoxypoly(oxy-1,2-ethanediyl)과 결합
  • 아스파라스
  • EZN-2285
  • SC-PEG 대장균 L-아스파라기나제
  • 석신이미딜 카보네이트 모노메톡시폴리에틸렌 글리콜 대장균 L-아스파라기나제
  • Calaspargase Pegol-mknl
절차: 생물 표본 수집
CSF 및 혈액 샘플 채취
다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
절차: 골수 흡인
골수 생검 및 흡인
절차: 심 초음파 검사
에코를받습니다
다른 이름들:
  • 심초음파
  • EC
실험적: Cohort B (revumenib and blinatumomab)
See Detailed Description.
의약품: 다우노루비신염산염
주어진 IV
다른 이름들:
  • 세루비딘
  • 클로리드라토 데 다우노루비시나
  • 다우노블라스틴
  • 다우노블라스티나
  • 다우노마이신염산염
  • 다우노마이신, 염산염
  • 다우노루비신.HCl
  • 다우노루비시니 염산염
  • FI-6339
  • 온데나
  • RP-13057
  • 루비도마이신 염산염
  • 루비렘
의약품: 덱사메타손
주어진 PO 또는 IV
다른 이름들:
  • 데카드론
  • 헤마디
  • Aacidexam
  • 아덱손
  • 아크니히톨 덱사
  • 알바덱스
  • 알린
  • 알린 디포
  • 알린 오프탈미코
  • 증폭
  • 안물모노
  • 오리쿨라룸
  • 옥실로손
  • 베이카드론
  • 바이큐텐
  • 베이큐튼 N
  • 코르티덱사손
  • 코르티섬만
  • 데카코트
  • 데카드롤
  • 데카드론 DP
  • 데칼릭스
  • 데카메스
  • 데카손 R.p.
  • 데탄실
  • 델타플루오렌
  • 데로닐
  • 데사메타손
  • 데사메톤
  • 덱사-마말렛
  • 덱사-코뿔소
  • 덱사-스케로손
  • 덱사 사인
  • 덱사피질
  • 덱사코르틴
  • 덱사파마
  • 덱사플루오렌
  • 덱사로컬
  • 덱사메코르틴
  • 덱사메스
  • 덱사메타손 인텐솔
  • 덱사메타소눔
  • 덱사모노존
  • 덱사포스
  • 덱시노랄
  • 덱손
  • 다이노르몬
  • 드제보
  • 플루오로델타
  • 포르테코틴
  • 감마코르텐
  • 헥사데카드롤
  • 헥사드롤
  • 로컬리슨-F
  • 로베린
  • 메틸플루오르프레드니솔론
  • 밀리코트
  • 마이메타손
  • 오르가드론
  • 스퍼사덱스
  • 테이퍼덱스
  • 비스메타존
  • 조덱스
  • 레나덱스
의약품: 빈크리스틴
주어진 IV
다른 이름들:
  • VCR
  • 류로크리스틴
  • 빈크리스틴
  • LCR
생물학적: 블리나투모맙
주어진 IV
다른 이름들:
  • 블린사이토
  • 항-CD19 x 항-CD3 이중특이성 단클론항체
  • 항-CD19/항-CD3 재조합 이중특이성 단클론 항체 MT103
  • 메디-538
  • MT-103
  • AMG 103
  • MT103
  • AMG103
  • MEDI538
  • AMG-103
  • 메디 538
  • MT 103
절차: 양전자 방출 단층 촬영
PET/CT를 받다
다른 이름들:
  • 의료 영상, 양전자 방출 단층 촬영
  • 애완 동물
  • PET 스캔
  • 양전자 방출 단층 촬영 스캔
  • 양전자 방출 단층 촬영
  • PT
  • 양전자방출단층촬영(시술)
절차: 골수 생검
골수 생검 및 흡인
다른 이름들:
  • 골수 생검
  • 생검, 골수
의약품: 메토트렉세이트
주어진 IT 또는 IV
다른 이름들:
  • 아비트렉세이트
  • 폴렉스
  • 멕세이트
  • MTX
  • 알파-메토프테린
  • 아메토프테린
  • 브라멕세이트
  • CL 14377
  • CL-14377
  • Emtexate
  • Emthexat
  • Emthexate
  • 파미트렉사트
  • 폴덱사토
  • 폴렉스 PFS
  • 란타렐
  • 레더트렉세이트
  • 루멕슨
  • 맥스렉스
  • 메드사트렉세이트
  • 메텍스
  • 메토블라스틴
  • 메토트렉세이트 LPF
  • 메토트렉세이트 메틸아미노프테린
  • 메토트렉사툼
  • 메토트렉사토
  • 메트로텍스
  • 멕세이트-AQ
  • 노바트렉스
  • 류마트렉스
  • 텍세이트
  • 트레메텍스
  • 트렉세론
  • 트리실렘
  • WR-19039
  • 질람보
의약품: 시타라빈
주어진 IV 또는 SC
다른 이름들:
  • .베타.-시토신 아라비노사이드
  • 1-.베타.-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-.beta.-D-Arabinofuranosylcytosine
  • 1-베타-D-아라비노푸라노실-4-아미노-2(1H)피리미디논
  • 1-베타-D-아라비노푸라노실시토신
  • 1.베타.-D-아라비노푸라노실시토신
  • 2(1H)-피리미디논, 4-아미노-1-베타-D-아라비노푸라노실-
  • 2(1H)-피리미디논, 4-아미노-1.베타.-D-아라비노푸라노실-
  • 알렉산
  • 아라씨
  • ARA 세포
  • 아라빈
  • 아라비노푸라노실시토신
  • 아라비노실시토신
  • 아라시티딘
  • 아라시티틴
  • 베타-시토신 아라비노사이드
  • CHX-3311
  • 시타라비눔
  • 시타벨
  • 사이토사르
  • 시토신 아라비노사이드
  • 시토신-.베타.-아라비노사이드
  • 시토신-베타-아라비노사이드
  • 에르팔파
  • 스타라시드
  • 타라빈 PFS
  • 유 19920
  • U-19920
  • 우디실
  • WR-28453
절차: 컴퓨터 단층 촬영
CT 또는 PET/CT를 받다
다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
절차: 생물 표본 수집
CSF 및 혈액 샘플 채취
다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
의약품: 레부메닙
주어진 PO
다른 이름들:
  • 메닌-혼합 계통 백혈병 단백질-단백질 상호작용 억제제 SNDX-5613
  • Menin-MLL 억제제 SNDX-5613
  • Menin-MLL 상호작용 억제제 SNDX-5613
  • SNDX 5613
  • SNDX-5613
  • SNDX5613
절차: 골수 흡인
골수 생검 및 흡인

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Dose limiting toxicities (Safety run-in: Cohort A)
기간: During cycle 1 (cycle 1 length = 28 days)
Will be evaluated using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v) 6.0. Will evaluate the proportion of participants with dose limiting toxicities and exact confidence intervals.
During cycle 1 (cycle 1 length = 28 days)
Measurable residual disease (MRD) negativity rate (Cohort A)
기간: Up to 35 days after start of therapy
Difference in proportion of participants who achieve clonoSEQ MRD status between the two arms will be compared using a two-sample proportion test.
Up to 35 days after start of therapy
MRD-event-free survival (EFS) (Cohort A)
기간: From date of randomization and up to 10 years
Will be compared using unstratified log-rank test.
From date of randomization and up to 10 years
Incidence of toxicities of interest (TOI) (Cohort B)
기간: Up to 30 days after last dose of study treatment
TOI rates will be reported with exact 90% confidence intervals.
Up to 30 days after last dose of study treatment

2차 결과 측정

결과 측정
측정값 설명
기간
Incidence of adverse events
기간: Up to 30 days after last dose of study treatment
Frequency and severity within each arm and across cycles of therapy will be assessed using NCI CTCAE v 6.0.
Up to 30 days after last dose of study treatment
MRD negative complete remission (CR) rate (Cohort A)
기간: Up to 70 days after start of therapy
Will be evaluated in participants with positive MRD before randomization.
Up to 70 days after start of therapy
EFS (Cohort A)
기간: At 6 months
Will be estimated using the Kaplan-Meier method. Will be evaluated in participants with negative MRD before randomization.
At 6 months
MRD-EFS (Cohort A)
기간: At 6 months
Will be estimated using the Kaplan-Meier method. Will be evaluated in participants with negative MRD before randomization.
At 6 months
Composite morphological CR rate (Cohort B)
기간: Up to 35 days after start of therapy
Will be defined as CR/CR with incomplete count recovery (CRi).
Up to 35 days after start of therapy
Proportion of participants MRD negative (Cohorts A and B)
기간: Up to 35 days after start of therapy
Will be evaluated using multi-color flow cytometry.
Up to 35 days after start of therapy
Rate of lineage switch and/or CD19-negative relapse (within each arm and cohort cohort)
기간: Up to 10 years
Up to 10 years
Rate of allogeneic hematopoietic stem cell transplantation utilization (within each arm and cohort cohort)
기간: Up to 10 years
Up to 10 years
EFS (within each arm and cohort cohort)
기간: From the date of trial registration/randomization until the first of death from any cause, relapse from remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Will be reported within each arm and cohort and by age. Will be estimated using the Kaplan-Meier method.
From the date of trial registration/randomization until the first of death from any cause, relapse from remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
MRD-EFS (within each arm and cohort cohort)
기간: From the date of trial registration/randomization until the first of death from any cause, relapse from remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Will be reported within each arm and cohort and by age. Will be estimated using the Kaplan-Meier method.
From the date of trial registration/randomization until the first of death from any cause, relapse from remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Relapse-free survival (within each arm and cohort cohort)
기간: From date of trial registration until relapse from CR/CRi or death from any cause, assessed up to 10 years
Will be reported within each arm and cohort and by age. Will be estimated using the Kaplan-Meier method.
From date of trial registration until relapse from CR/CRi or death from any cause, assessed up to 10 years
Progression-free survival (PFS) (within each arm and cohort cohort)
기간: From the date of trial registration/randomization until the first of progression, death from any cause, relapse from morphologic remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Will be reported within each arm and cohort and by age. Will be estimated using the Kaplan-Meier method.
From the date of trial registration/randomization until the first of progression, death from any cause, relapse from morphologic remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
MRD-PFS (within each arm and cohort cohort)
기간: From the date of trial registration/randomization until the first of progression, death from any cause, relapse from morphologic remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Will be reported within each arm and cohort and by age. Will be estimated using the Kaplan-Meier method.
From the date of trial registration/randomization until the first of progression, death from any cause, relapse from morphologic remission, secondary malignancy, or completion of protocol therapy, assessed up to 10 years
Time to MRD relapse (within each arm and cohort cohort)
기간: Up to 10 years
Will be assessed using flow cytometry and/or clonoSEQ.
Up to 10 years
Overall survival (within each arm and cohort cohort)
기간: From day of trial registration until death from any cause, assessed up to 10 years
Will be estimated using the Kaplan-Meier method.
From day of trial registration until death from any cause, assessed up to 10 years
Remission rate
기간: Up to 10 years
Will be defined as CR/CRi/CR with partial hematological recovery) with and without MRD by flow. Will be estimated with 95% binomial confidence intervals.
Up to 10 years

기타 결과 측정

결과 측정
측정값 설명
기간
Frequency of MEN1 mutations
기간: Up to 10 years after start of therapy
Will be evaluated by quantitative polymerase chain reaction (PCR) and/or high sensitivity next generation sequencing.
Up to 10 years after start of therapy
Rate of KMT2A fusion reverse transcriptase (RT)-PCR MRD negativity within treatment arms (Cohort A)
기간: After the first and second cycle of blinatumomab (cycle length = 28 days)
After the first and second cycle of blinatumomab (cycle length = 28 days)
KMT2A fusion RT-PCR MRD negativity (Cohort B)
기간: Up to 90 days after start of therapy
Up to 90 days after start of therapy
Rate of IG/TR V(D)J MRD negative remission
기간: Up to 35 days after start of therapy
Up to 35 days after start of therapy
Changes in gene expression between diagnosis (in Cohort B and as available in Cohort A) and relapse samples
기간: Up to 10 years
Up to 10 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

SWOG Cancer Research Network

협력자

National Cancer Institute (NCI)

수사관

  • 수석 연구원: Ibrahim Aldoss, SWOG Cancer Research Network

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 10월 14일

기본 완료 (추정된)

2031년 4월 16일

연구 완료 (추정된)

2032년 4월 16일

연구 등록 날짜

최초 제출

2026년 5월 22일

QC 기준을 충족하는 최초 제출

2026년 6월 3일

처음 게시됨 (실제)

2026년 6월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 3일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • S2507 (기타 식별자: CTEP)
  • U10CA180888 (미국 NIH 보조금/계약)
  • NCI-2026-03381 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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