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Prueba de la adición de venetoclax o gemtuzumab ozogamicina (GO) al régimen de tratamiento habitual (citarabina y daunorubicina, "7+3") para el factor de unión central leucemia mieloide aguda (CBF-AML) para mejorar la respuesta (un ensayo de tratamiento de mielomatch)

3 de noviembre de 2026 actualizado por: National Cancer Institute (NCI)

Estudio de fase II de citarabina + daunorrubicina (7 + 3) + gemtuzumab ozogamicina vs. citarabina + daunorubicina (7 + 3) + Venetoclax para el tratamiento de la mieloides de unión núcleo recién diagnosticado (CBF-AML) en adultos jóvenes: un subestudio de mielónimo: A Myelomatch Sustudy

This phase II MYELOMATCH treatment trial compares the effect of venetoclax to gemtuzumab ozogamicin, when given with cytarabine and daunorubicin ("7+3" regimen), for the treatment of patients with core binding factor acute myeloid leukemia (CBF-AML). Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Gemtuzumab ozogamicin is a monoclonal antibody, called gemtuzumab, linked to an antitumor antibiotic drug, called ozogamicin. Gemtuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as CD33 receptors, and delivers ozogamicin to kill them. Chemotherapy drugs, such as cytarabine 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. Giving venetoclax with cytarabine and daunorubicin may have fewer side effects and be as effective or better than the combination with gemtuzumab ozogamicin in treating patients with core binding factor AML.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Intervención / Tratamiento

Descripción detallada

PRIMARY OBJECTIVE:

I. Compare the rates of complete remission (CR) without measurable residual disease (CRMRD-) by multiparameter flow cytometry following induction therapy between the two treatment arms in each cohort separately.

SECONDARY OBJECTIVES:

I. To compare the rates of CR and composite complete remission (CRc) (CR+complete remission with incomplete hematologic recovery [CRi]+complete remission with partial hematologic recovery [CRh]) between the treatment arms.

II. To compare the overall survival (OS) between the treatment arms. III. To compare the event-free survival (EFS). IV. To compare the cumulative incidence of relapse (CIR). V. To compare the cumulative incidence of death (CID) between the treatment arms.

VI. To compare the rate of early death at 30 days and 60 days between the treatment arms.

VII. To assess the rate and frequency of adverse events between treatment arms. VIII. To evaluate mutant RAS and mutant KIT as predictive biomarkers for CRMRD- rate in CBF AML.

EXPLORATORY OBJECTIVE:

I. To compare MRD (and its clinical implication, e.g., relapse rates) between flow cytometry (FC) and next generation sequencing (NGS)-based (RUNX1::RUNX1T1 or CBFB::MYH11).

CORRELATIVE OBJECTIVES:

I. To evaluate the frequency and clinical impact of variant allele frequency (VAF) of KIT mutation, KIT mutations in different exons (e.g., exon 8 or 17), CD33 expression, additional (secondary) mutations and cytogenetic abnormalities.

II. To evaluate the differences in clinical and molecular outcomes in patients with RUNX1::RUNX1T1 mutated versus CBFB::MYH11 mutated CBF AML.

OUTLINE: Patients are randomized to 1 of 2 regimens.

REGIMEN 1: Patients receive gemtuzumab ozogamicin intravenously (IV) on day 1, 2 or 3 and on day 4, 5, or 6 (NOTE: two doses must be at least 3 days apart), as well as cytarabine IV, continuously, on days 1-7 and daunorubicin IV on days 1-3 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or multigated acquisition (MUGA) scan during screening, as well as bone marrow aspiration and blood sample collection throughout the study.

REGIMEN 2: Patients receive venetoclax orally (PO) once daily (QD) on days 1-11, cytarabine IV, continuously, on days 2-8 and daunorubicin IV on days 2-4 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening and bone marrow aspiration, as well as blood sample collection throughout the study.

After completion of study treatment, patients are followed up at relapse and every 3 months for 2 years, then every 6 months until 5 years.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

162

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Estados Unidos
    • Alabama
      • Birmingham, Alabama, Estados Unidos, 35233
        • Reclutamiento
        • University of Alabama at Birmingham Cancer Center
        • Investigador principal:
          • Razan Mohty
        • Contacto:
    • California
      • La Jolla, California, Estados Unidos, 92093
        • Reclutamiento
        • UC San Diego Moores Cancer Center
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 858-822-5354
          • Correo electrónico: cancercto@ucsd.edu
        • Investigador principal:
          • Tiffany N. Tanaka
    • Florida
      • Pembroke Pines, Florida, Estados Unidos, 33028
        • Reclutamiento
        • Memorial Hospital West
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 954-265-4325
        • Investigador principal:
          • Yehuda E. Deutsch
    • Idaho
      • Coeur d'Alene, Idaho, Estados Unidos, 83814
        • Reclutamiento
        • Kootenai Health - Coeur d'Alene
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Post Falls, Idaho, Estados Unidos, 83854
        • Reclutamiento
        • Kootenai Clinic Cancer Services - Post Falls
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Sandpoint, Idaho, Estados Unidos, 83864
        • Reclutamiento
        • Kootenai Clinic Cancer Services - Sandpoint
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
    • Illinois
      • Chicago, Illinois, Estados Unidos, 60637
        • Reclutamiento
        • University of Chicago Comprehensive Cancer Center
        • Contacto:
        • Investigador principal:
          • Olatoyosi M. Odenike
      • Chicago, Illinois, Estados Unidos, 60611
        • Reclutamiento
        • Northwestern University
        • Contacto:
        • Investigador principal:
          • Yuchen Liu
      • Chicago, Illinois, Estados Unidos, 60612
        • Reclutamiento
        • University of Illinois
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 312-355-3046
        • Investigador principal:
          • Noah Birch
      • Chicago, Illinois, Estados Unidos, 60612
        • Reclutamiento
        • Rush MD Anderson Cancer Center
        • Contacto:
        • Investigador principal:
          • Melissa L. Larson
      • New Lenox, Illinois, Estados Unidos, 60451
        • Reclutamiento
        • UC Comprehensive Cancer Center at Silver Cross
        • Contacto:
        • Investigador principal:
          • Olatoyosi M. Odenike
      • Orland Park, Illinois, Estados Unidos, 60462
        • Reclutamiento
        • University of Chicago Medicine-Orland Park
        • Contacto:
        • Investigador principal:
          • Olatoyosi M. Odenike
    • Indiana
      • Crown Point, Indiana, Estados Unidos, 46307
        • Reclutamiento
        • UChicago Medicine Northwest Indiana
        • Investigador principal:
          • Olatoyosi M. Odenike
        • Contacto:
    • Kansas
      • Fairway, Kansas, Estados Unidos, 66205
        • Reclutamiento
        • University of Kansas Clinical Research Center
        • Contacto:
        • Investigador principal:
          • Jesus Gonzalez Lugo
      • Kansas City, Kansas, Estados Unidos, 66160
        • Reclutamiento
        • University of Kansas Cancer Center
        • Contacto:
        • Investigador principal:
          • Jesus Gonzalez Lugo
      • Overland Park, Kansas, Estados Unidos, 66211
        • Reclutamiento
        • University of Kansas Hospital-Indian Creek Campus
        • Contacto:
        • Investigador principal:
          • Jesus Gonzalez Lugo
      • Westwood, Kansas, Estados Unidos, 66205
        • Reclutamiento
        • University of Kansas Hospital-Westwood Cancer Center
        • Contacto:
        • Investigador principal:
          • Jesus Gonzalez Lugo
    • Kentucky
      • Lexington, Kentucky, Estados Unidos, 40536
        • Reclutamiento
        • University of Kentucky/Markey Cancer Center
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 859-257-3379
        • Investigador principal:
          • Fevzi Yalniz
      • Louisville, Kentucky, Estados Unidos, 40202
        • Reclutamiento
        • The James Graham Brown Cancer Center at University of Louisville
        • Investigador principal:
          • Mohamed M. Hegazi
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 502-562-3429
      • Louisville, Kentucky, Estados Unidos, 40245
        • Reclutamiento
        • UofL Health Medical Center Northeast
        • Investigador principal:
          • Mohamed M. Hegazi
        • Contacto:
    • Louisiana
      • Baton Rouge, Louisiana, Estados Unidos, 70808
        • Reclutamiento
        • Our Lady of the Lake Physician Group
        • Contacto:
        • Investigador principal:
          • Harry G. Sequeira Gross
    • Massachusetts
      • Boston, Massachusetts, Estados Unidos, 02215
        • Reclutamiento
        • Dana-Farber Cancer Institute
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 877-442-3324
        • Investigador principal:
          • Eric S. Winer
      • Boston, Massachusetts, Estados Unidos, 02111
    • Michigan
      • Brighton, Michigan, Estados Unidos, 48114
        • Reclutamiento
        • Trinity Health IHA Medical Group Hematology Oncology - Brighton
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
      • Canton, Michigan, Estados Unidos, 48188
        • Reclutamiento
        • Trinity Health IHA Medical Group Hematology Oncology - Canton
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
      • Chelsea, Michigan, Estados Unidos, 48118
        • Reclutamiento
        • Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
      • Livonia, Michigan, Estados Unidos, 48154
        • Reclutamiento
        • Trinity Health Saint Mary Mercy Livonia Hospital
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
      • Pontiac, Michigan, Estados Unidos, 48341
        • Reclutamiento
        • Trinity Health Saint Joseph Mercy Oakland Hospital
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
      • Ypsilanti, Michigan, Estados Unidos, 48197
        • Reclutamiento
        • Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
        • Contacto:
        • Investigador principal:
          • Tareq Al baghdadi
    • Mississippi
      • Columbus, Mississippi, Estados Unidos, 39705
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Golden Triangle
        • Investigador principal:
          • Salil Goorha
        • Contacto:
      • Grenada, Mississippi, Estados Unidos, 38901
        • Reclutamiento
        • Baptist Cancer Center-Grenada
        • Investigador principal:
          • Salil Goorha
        • Contacto:
      • New Albany, Mississippi, Estados Unidos, 38652
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Union County
        • Investigador principal:
          • Salil Goorha
        • Contacto:
      • Oxford, Mississippi, Estados Unidos, 38655
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Oxford
        • Investigador principal:
          • Salil Goorha
        • Contacto:
      • Southhaven, Mississippi, Estados Unidos, 38671
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Desoto
        • Investigador principal:
          • Salil Goorha
        • Contacto:
    • Missouri
      • City of Saint Peters, Missouri, Estados Unidos, 63376
        • Reclutamiento
        • Siteman Cancer Center at Saint Peters Hospital
        • Contacto:
        • Investigador principal:
          • Ramzi Abboud
      • Creve Coeur, Missouri, Estados Unidos, 63141
        • Reclutamiento
        • Siteman Cancer Center at West County Hospital
        • Contacto:
        • Investigador principal:
          • Ramzi Abboud
      • St Louis, Missouri, Estados Unidos, 63110
        • Reclutamiento
        • Washington University School of Medicine
        • Contacto:
        • Investigador principal:
          • Ramzi Abboud
      • St Louis, Missouri, Estados Unidos, 63129
        • Reclutamiento
        • Siteman Cancer Center-South County
        • Contacto:
        • Investigador principal:
          • Ramzi Abboud
      • St Louis, Missouri, Estados Unidos, 63136
        • Reclutamiento
        • Siteman Cancer Center at Christian Hospital
        • Contacto:
        • Investigador principal:
          • Ramzi Abboud
    • Montana
      • Anaconda, Montana, Estados Unidos, 59711
        • Reclutamiento
        • Community Hospital of Anaconda
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Billings, Montana, Estados Unidos, 59101
        • Reclutamiento
        • Billings Clinic Cancer Center
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Bozeman, Montana, Estados Unidos, 59715
        • Reclutamiento
        • Bozeman Health Deaconess Hospital
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Great Falls, Montana, Estados Unidos, 59405
        • Reclutamiento
        • Benefis Sletten Cancer Institute
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Kalispell, Montana, Estados Unidos, 59901
        • Reclutamiento
        • Logan Health Medical Center
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
      • Missoula, Montana, Estados Unidos, 59804
        • Reclutamiento
        • Community Medical Center
        • Investigador principal:
          • John M. Schallenkamp
        • Contacto:
    • Nebraska
      • Bellevue, Nebraska, Estados Unidos, 68123
        • Reclutamiento
        • Nebraska Medicine-Bellevue
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 402-559-6941
          • Correo electrónico: unmcrsa@unmc.edu
        • Investigador principal:
          • Michael Haddadin
      • Omaha, Nebraska, Estados Unidos, 68198
        • Reclutamiento
        • University of Nebraska Medical Center
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 402-559-6941
          • Correo electrónico: unmcrsa@unmc.edu
        • Investigador principal:
          • Michael Haddadin
      • Omaha, Nebraska, Estados Unidos, 68118
        • Reclutamiento
        • Nebraska Medicine-Village Pointe
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 402-559-5600
        • Investigador principal:
          • Michael Haddadin
    • New Mexico
      • Albuquerque, New Mexico, Estados Unidos, 87106
        • Reclutamiento
        • University of New Mexico Cancer Center
        • Contacto:
        • Investigador principal:
          • Charles Foucar
    • New York
      • Buffalo, New York, Estados Unidos, 14263
        • Reclutamiento
        • Roswell Park Cancer Institute
        • Investigador principal:
          • Eunice S. Wang
        • Contacto:
      • Rochester, New York, Estados Unidos, 14642
        • Reclutamiento
        • University of Rochester
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 585-275-5830
        • Investigador principal:
          • Bassil Botros
      • Syracuse, New York, Estados Unidos, 13210
        • Reclutamiento
        • State University of New York Upstate Medical University
        • Investigador principal:
          • Teresa C. Gentile
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 315-464-5476
      • The Bronx, New York, Estados Unidos, 10467
        • Reclutamiento
        • Montefiore Medical Center - Moses Campus
        • Investigador principal:
          • Ioannis Mantzaris
        • Contacto:
    • North Carolina
      • Durham, North Carolina, Estados Unidos, 27710
        • Reclutamiento
        • Duke University Medical Center
        • Investigador principal:
          • Harry P. Erba
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 888-275-3853
    • Ohio
      • Columbus, Ohio, Estados Unidos, 43210
        • Reclutamiento
        • Ohio State University Comprehensive Cancer Center
        • Investigador principal:
          • Alice S. Mims
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 800-293-5066
          • Correo electrónico: Jamesline@osumc.edu
    • Oklahoma
      • Oklahoma City, Oklahoma, Estados Unidos, 73104
        • Reclutamiento
        • University of Oklahoma Health Sciences Center
        • Contacto:
        • Investigador principal:
          • Zimu Gong
    • Pennsylvania
      • Danville, Pennsylvania, Estados Unidos, 17822
        • Reclutamiento
        • Geisinger Medical Center
        • Investigador principal:
          • Joseph J. Vadakara
        • Contacto:
      • Wilkes-Barre, Pennsylvania, Estados Unidos, 18711
        • Reclutamiento
        • Geisinger Wyoming Valley/Henry Cancer Center
        • Contacto:
        • Investigador principal:
          • Joseph J. Vadakara
    • Rhode Island
      • Providence, Rhode Island, Estados Unidos, 02903
        • Reclutamiento
        • Rhode Island Hospital
        • Investigador principal:
          • John L. Reagan
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 401-444-1488
    • South Carolina
      • Boiling Springs, South Carolina, Estados Unidos, 29316
        • Reclutamiento
        • Prisma Health Cancer Institute - Spartanburg
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Easley, South Carolina, Estados Unidos, 29640
        • Reclutamiento
        • Prisma Health Cancer Institute - Easley
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Greenville, South Carolina, Estados Unidos, 29605
        • Reclutamiento
        • Prisma Health Cancer Institute - Faris
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Greenville, South Carolina, Estados Unidos, 29605
        • Reclutamiento
        • Prisma Health Cancer Institute - Butternut
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Greenville, South Carolina, Estados Unidos, 29615
        • Reclutamiento
        • Prisma Health Cancer Institute - Eastside
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Greer, South Carolina, Estados Unidos, 29650
        • Reclutamiento
        • Prisma Health Cancer Institute - Greer
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
      • Seneca, South Carolina, Estados Unidos, 29672
        • Reclutamiento
        • Prisma Health Cancer Institute - Seneca
        • Investigador principal:
          • Suzanne R. Fanning
        • Contacto:
    • Tennessee
      • Collierville, Tennessee, Estados Unidos, 38017
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Collierville
        • Investigador principal:
          • Salil Goorha
        • Contacto:
      • Memphis, Tennessee, Estados Unidos, 38120
        • Reclutamiento
        • Baptist Memorial Hospital and Cancer Center-Memphis
        • Investigador principal:
          • Salil Goorha
        • Contacto:
    • Utah
      • Salt Lake City, Utah, Estados Unidos, 84112
        • Reclutamiento
        • Huntsman Cancer Institute/University of Utah
        • Contacto:
        • Investigador principal:
          • Paul J. Shami
    • Virginia
      • Richmond, Virginia, Estados Unidos, 23298
        • Reclutamiento
        • VCU Massey Comprehensive Cancer Center
        • Investigador principal:
          • Keri R. Maher
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 804-628-6430
          • Correo electrónico: CTOclinops@vcu.edu
    • Washington
      • Edmonds, Washington, Estados Unidos, 98026
        • Reclutamiento
        • Swedish Cancer Institute-Edmonds
        • Investigador principal:
          • Alison K. Conlin
        • Contacto:
      • Issaquah, Washington, Estados Unidos, 98029
        • Reclutamiento
        • Swedish Cancer Institute-Issaquah
        • Investigador principal:
          • Alison K. Conlin
        • Contacto:
      • Seattle, Washington, Estados Unidos, 98122
        • Reclutamiento
        • Swedish Medical Center-First Hill
        • Investigador principal:
          • Alison K. Conlin
        • Contacto:
    • Wisconsin
      • La Crosse, Wisconsin, Estados Unidos, 54601
        • Reclutamiento
        • Gundersen Lutheran Medical Center
        • Contacto:
        • Investigador principal:
          • Michael O. Ojelabi
      • Menomonee Falls, Wisconsin, Estados Unidos, 53051
        • Reclutamiento
        • Froedtert Menomonee Falls Hospital
        • Investigador principal:
          • Ehab L. Atallah
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 262-257-5100
      • Milwaukee, Wisconsin, Estados Unidos, 53226
        • Reclutamiento
        • Medical College of Wisconsin
        • Investigador principal:
          • Ehab L. Atallah
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 414-805-3666
      • New Berlin, Wisconsin, Estados Unidos, 53151
        • Reclutamiento
        • Froedtert and MCW Moorland Reserve Health Center
        • Investigador principal:
          • Ehab L. Atallah
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 414-805-0505
      • Oak Creek, Wisconsin, Estados Unidos, 53154
        • Reclutamiento
        • Drexel Town Square Health Center
        • Investigador principal:
          • Ehab L. Atallah
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 414-805-0505
      • West Bend, Wisconsin, Estados Unidos, 53095
        • Reclutamiento
        • Froedtert West Bend Hospital/Kraemer Cancer Center
        • Investigador principal:
          • Ehab L. Atallah
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 414-805-0505
  • Puerto Rico
      • San Juan, Puerto Rico, 00927
        • Reclutamiento
        • Centro Comprensivo de Cancer de UPR
        • Investigador principal:
          • Luis J. Santos Reyes
        • Contacto:
      • San Juan, Puerto Rico, 00936
        • Reclutamiento
        • San Juan City Hospital
        • Investigador principal:
          • Luis J. Santos Reyes
        • Contacto:
          • Site Public Contact
          • Número de teléfono: 787-763-1296

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 59 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • GENERAL MYELOMATCH CRITERIA: Patients must be registered to the Master Screening and Reassessment Protocol, MYELOMATCH, and assigned to this protocol by the MATCHBox Treatment Verification Team

  • GENERAL MYELOMATCH CRITERIA: Participants must not have received prior anti-cancer therapy for AML or myelodysplastic syndrome (MDS)

    • Note: Hydroxyurea to control the white blood cell count (WBC) and cytarabine up to 1g for urgent cytoreduction is allowed.
    • Note: Prior erythroid stimulating agent (ESA) is not considered prior therapy for the purposes of eligibility

  • GENERAL MYELOMATCH CRITERIA: Participants must not receive any cytarabine-containing therapy other than up to 1g of cytarabine, which is allowed for urgent cytoreduction. Hydroxyurea, all-trans retinoic acid (ATRA), BCR-ABL directed tyrosine kinase inhibitor, erythropoiesis-stimulating agent, thrombopoietin receptor agonist and lenalidomide is allowed

  • Diagnosis of AML with t(8;21)(q22;q22.1)/RUNX1::RUNX1T1 or AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)/CBFB::MYH11. No FLT3 mutation (these patients should be considered for a FLT3-focused MYELOMATCH study)

  • Secondary CBF-AML (e.g., prior pre-leukemic hematologic malignancy or history of chemotherapy/radiation therapy) is allowed.

  • No prior AML or MDS-directed therapy except for urgent treatment of leukocytosis with leukapheresis, cytarabine, and hydroxyurea, Prior intrathecal chemotherapy for central nervous system (CNS) involvement of AML is permitted

  • Age 18-59 years

  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 3

  • Total bilirubin ≤ 1.5 x upper limit of normal (ULN) (unless patient has a history of Gilbert syndrome and direct bilirubin is ≤ 1.5 x ULN)

  • Aspartate aminotransferase (AST)(serum glutamic oxaloacetic transaminase [SGOT])/ alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) ≤ 3 x upper limit of normal (ULN)

  • Glomerular filtration rate (GFR) ≥ 30 mL/min/1.73m^2

  • Not pregnant and not nursing, because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown. Therefore, for women of childbearing potential only, a negative urine or serum pregnancy test done ≤ 7 days prior to registration is required

  • Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial

  • Participants with CNS disease are eligible for this trial and will be treated according to institutional guidelines with intrathecal chemotherapy for this aspect of their disease

  • Patients with known HIV infection on effective anti-retroviral therapy with undetectable viral load within 6 months prior to registration 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

  • Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class II or better

  • No known medical condition causing an inability to swallow oral formulations of agents

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Regimen 1 (gemtuzumab ozogamicin 7+3)

Patients receive gemtuzumab ozogamicin IV on day 1, 2 or 3 and on day 4, 5, or 6 (NOTE: two doses must be at least 3 days apart), as well as cytarabine IV, continuously, on days 1-7 and daunorubicin IV on days 1-3 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening, as well as bone marrow aspiration and blood sample collection throughout the study.
Droga: Cytarabine

Given IV

Otros nombres:
  • .beta.-Arabinósido de citosina
  • 1-.beta.-D-Arabinofuranosil-4-amino-2(1H)pirimidinona
  • 1-.beta.-D-Arabinofuranosilcitosina
  • 1-Beta-D-arabinofuranosil-4-amino-2(1H)pirimidinona
  • 1-Beta-D-arabinofuranosilcitosina
  • 1.beta.-D-Arabinofuranosilcitosina
  • 2(1H)-pirimidinona, 4-amino-1-beta-D-arabinofuranosil-
  • 2(1H)-pirimidinona, 4-amino-1.beta.-D-arabinofuranosil-
  • Alexán
  • Ara-C
  • Célula ARA
  • Arabe
  • Arabinofuranosilcitosina
  • Arabinosilcitosina
  • Aracitidina
  • Aracitina
  • Arabinósido de beta-citosina
  • CHX-3311
  • Citarabino
  • Citarbel
  • Citosar
  • Arabinósido de citosina
  • Citosina-.beta.-arabinósido
  • Citosina-beta-arabinósido
  • Erpalfa
  • Starasid
  • Tarabina SLP
  • U 19920
  • U-19920
  • Udicilo
  • WR-28453
Droga: Gemtuzumab Ozogamicin

Given IV

Otros nombres:
  • Milotarg
  • Anticuerpo monoclonal humanizado anti-CD33 conjugado con caliqueamicina
  • CDP-771
  • CMA-676
  • gemtuzumab
  • hP67.6-Caliqueamicina
  • WAY-CMA-676
Procedimiento: Biospecimen Collection

Undergo blood sample collection

Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Procedimiento: Bone Marrow Aspiration

Undergo bone marrow aspiration

Droga: Daunorubicin Hydrochloride

Given IV

Otros nombres:
  • Cerubidina
  • Cloridrato de daunorubicina
  • Daunoblastina
  • Clorhidrato de daunomicina
  • Daunomicina, clorhidrato
  • Daunorubicina.HCl
  • Clorhidrato de Daunorubicini
  • FI-6339
  • Ondeña
  • RP-13057
  • Clorhidrato de rubidomicina
  • Rubilem
Procedimiento: Multigated Acquisition Scan

Undergo MUGA scan

Otros nombres:
  • Exploración de la piscina de sangre
  • Angiografía con radionúclidos de equilibrio
  • Imagen de piscina de sangre cerrada
  • MUGA
  • Ventriculografía con radionúclidos
  • RNVG
  • Escaneo SIMA
  • Escaneo de adquisición sincronizado de múltiples puertas
  • Escaneo MUGA
  • Escaneo de adquisición de puertas múltiples
  • Exploración de ventriculograma con radionúclidos
  • Escaneo de grupo de corazón cerrado
  • Escaneo RNV
Procedimiento: Echocardiography Test

Undergo echocardiography

Otros nombres:
  • Ecocardiografía
  • CE
Experimental: Regimen 2 (Venetoclax, 7+3)

Patients receive venetoclax orally (PO) once daily (QD) on days 1-11, cytarabine IV, continuously, on days 2-8 and daunorubicin IV on days 2-4 in the absence of disease progression or unacceptable toxicity. Patients then undergo standard of care consolidation/post-remission treatment at the discretion of the treating physician. Patients undergo echocardiography or MUGA scan during screening and bone marrow aspiration, as well as blood sample collection throughout the study.
Droga: Cytarabine

Given IV

Otros nombres:
  • .beta.-Arabinósido de citosina
  • 1-.beta.-D-Arabinofuranosil-4-amino-2(1H)pirimidinona
  • 1-.beta.-D-Arabinofuranosilcitosina
  • 1-Beta-D-arabinofuranosil-4-amino-2(1H)pirimidinona
  • 1-Beta-D-arabinofuranosilcitosina
  • 1.beta.-D-Arabinofuranosilcitosina
  • 2(1H)-pirimidinona, 4-amino-1-beta-D-arabinofuranosil-
  • 2(1H)-pirimidinona, 4-amino-1.beta.-D-arabinofuranosil-
  • Alexán
  • Ara-C
  • Célula ARA
  • Arabe
  • Arabinofuranosilcitosina
  • Arabinosilcitosina
  • Aracitidina
  • Aracitina
  • Arabinósido de beta-citosina
  • CHX-3311
  • Citarabino
  • Citarbel
  • Citosar
  • Arabinósido de citosina
  • Citosina-.beta.-arabinósido
  • Citosina-beta-arabinósido
  • Erpalfa
  • Starasid
  • Tarabina SLP
  • U 19920
  • U-19920
  • Udicilo
  • WR-28453
Procedimiento: Biospecimen Collection

Undergo blood sample collection

Otros nombres:
  • Recolección de muestras biológicas
  • Muestra biológica recolectada
  • Coleccion de especimenes
  • Recolección de muestras
Procedimiento: Bone Marrow Aspiration

Undergo bone marrow aspiration

Droga: Daunorubicin Hydrochloride

Given IV

Otros nombres:
  • Cerubidina
  • Cloridrato de daunorubicina
  • Daunoblastina
  • Clorhidrato de daunomicina
  • Daunomicina, clorhidrato
  • Daunorubicina.HCl
  • Clorhidrato de Daunorubicini
  • FI-6339
  • Ondeña
  • RP-13057
  • Clorhidrato de rubidomicina
  • Rubilem
Procedimiento: Multigated Acquisition Scan

Undergo MUGA scan

Otros nombres:
  • Exploración de la piscina de sangre
  • Angiografía con radionúclidos de equilibrio
  • Imagen de piscina de sangre cerrada
  • MUGA
  • Ventriculografía con radionúclidos
  • RNVG
  • Escaneo SIMA
  • Escaneo de adquisición sincronizado de múltiples puertas
  • Escaneo MUGA
  • Escaneo de adquisición de puertas múltiples
  • Exploración de ventriculograma con radionúclidos
  • Escaneo de grupo de corazón cerrado
  • Escaneo RNV
Droga: Venetoclax

Given PO

Otros nombres:
  • Venclexta
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • Venclyxto
  • AB 199
  • GDC 0199
  • GDC0199
Procedimiento: Echocardiography Test

Undergo echocardiography

Otros nombres:
  • Ecocardiografía
  • CE

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Complete remission without measurable residual disease (CRMRD-)
Periodo de tiempo: At end of induction (Up to 28 days)

MRD will be evaluated by Molecular Diagnostics Network flow cytometry and will be defined at a threshold of ≤ 10^-3.
At end of induction (Up to 28 days)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Rate of complete remission (CR)
Periodo de tiempo: At the end of treatment (Up to 28 days)

Defined as the number of evaluable patients achieving a response of CR per European Leukemia Network (ELN) 2022 criteria at the end of treatment divided by the total number of evaluable patients. Rates of response will be compared between treatment arms using a chi-square test (or Fisher's exact test as needed). Point estimates will be generated for CR rate within each arm along with 95% confidence intervals using the Clopper-Pearson method.
At the end of treatment (Up to 28 days)
Rate of composite CR
Periodo de tiempo: At the end of treatment (Up to 28 days)

Defined as the number of evaluable patients achieving a response of CR or complete remission with incomplete hematologic recovery (CRi) or complete remission with partial hematologic recovery (CRh) per ELN 2022 criteria at the end of treatment divided by the total number of evaluable patients. Rates of response will be compared between treatment arms using a chi-square test (or Fisher's exact test as needed). Point estimates will be generated for CR rate within each arm along with 95% confidence intervals using the Clopper-Pearson method.
At the end of treatment (Up to 28 days)
Overall survival (OS)
Periodo de tiempo: From registration until death due to any cause, up to 5 years

The distribution of OS will be estimated using method of Kaplan-Meier. The median OS and 95% confidence interval will be reported.
From registration until death due to any cause, up to 5 years
Event free survival (EVS)
Periodo de tiempo: From randomization to induction failure, hematologic relapse from CR/CRh/CRi or death from any cause, whichever occurs first, up to 5 years

Induction failure is defined as not achieving either CR, CRh or CRi by after induction therapy. The distribution of EFS will be estimated using method of Kaplan-Meier, and compared using log-rank tests. The median EFS and the corresponding 95% confidence interval will be reported.
From randomization to induction failure, hematologic relapse from CR/CRh/CRi or death from any cause, whichever occurs first, up to 5 years
Cumulative incidence of relapse (CIR)
Periodo de tiempo: From the date of achievement of a remission until the date of hematologic relapse, up to 5 years

The distribution of CIR will be estimated using Fine-Gray model and reported via hazard ratios and 95% confidence interval with p values.
From the date of achievement of a remission until the date of hematologic relapse, up to 5 years
Cumulative incidence of death (CID)
Periodo de tiempo: From the date of achievement of a remission to death without prior relapse, up to 5 years

The distribution of CID will be estimated using Fine-Gray model and reported via hazard ratios and 95% confidence interval with p values.
From the date of achievement of a remission to death without prior relapse, up to 5 years
Rate of early death at 30 days (ED-30)
Periodo de tiempo: At 30 days

ED-30 is defined as the total number of patients who died on or before day 30 from randomization divided by the total number of evaluable patients. Rate of early death at day 30 will be compared between treatment arms using a chi-square test (or Fisher's exact test as needed). Point estimates will be generated for ED-30 rate within each arm along with 95% confidence intervals using the Clopper-Pearson method.
At 30 days
Rate of early death at 60 days (ED-60)
Periodo de tiempo: At 60 days

ED-60 is defined as the total number of patients who died on or before day 60 from randomization divided by the total number of evaluable patients. Rate of early death at day 60 will be compared between treatment arms using a chi-square test (or Fisher's exact test as needed). Point estimates will be generated for ED-60 rate within each arm along with 95% confidence intervals using the Clopper-Pearson method.
At 60 days
Incidence of adverse events
Periodo de tiempo: Up to 5 years

As per national Cancer Institute Common Terminology Criteria for Adverse Events version 5.0. The maximum grade for each type of toxicity will be recorded for each patient, and frequency tables will be reviewed to determine toxicity patterns. The incidence of severe (grade 3+) adverse events or toxicities will be described for each treatment arm and will also be compared between the arms. Fisher's exact tests will be used to quantitatively compare the incidence of severe as well as specific toxicities of interest between the treatment arms and we will graphically assess differences in maximum grades observed for toxicities between the arms.
Up to 5 years
Evaluate mutant RAS and mutant KIT as predictive biomarkers for CRMRD- rate
Periodo de tiempo: Up to 5 years

In cohort 1, subgroup analysis will be conducted to evaluate the treatment effect among RAS mutated patients using Kaplan Meier methods and log-rank tests; similar subgroup analysis will be done among KIT mutated patients.
Up to 5 years

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

National Cancer Institute (NCI)

Investigadores

  • Investigador principal: Celalettin Ustun, Alliance for Clinical Trials in Oncology

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

28 de septiembre de 2026

Finalización primaria (Estimado)

25 de noviembre de 2027

Finalización del estudio (Estimado)

25 de noviembre de 2027

Fechas de registro del estudio

Enviado por primera vez

8 de abril de 2025

Primero enviado que cumplió con los criterios de control de calidad

8 de abril de 2025

Publicado por primera vez (Actual)

9 de abril de 2025

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • NCI-2025-02426
  • U10CA180821 (Subvención/contrato del NIH de EE. UU.)
  • NCI-2025-02426 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
  • MM1YA-A04 (Otro identificador: CTEP)
  • MM1YA-A04 (Otro identificador: Alliance for Clinical Trials in Oncology)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan 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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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