Venetoclax Combined With FLAG-IDA Induction and Consolidation in Newly Diagnosed and Relapsed or Refractory Acute Myeloid Leukemia

  • Courtney D. DiNardo
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Curtis A. Lachowiez
    Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Koichi Takahashi
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Sanam Loghavi
    Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Lianchun Xiao
    Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Tapan Kadia
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Naval Daver
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Maria Adeoti
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Nicholas J. Short
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Koji Sasaki
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Sa Wang
    Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Gautam Borthakur
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Ghayas Issa
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Abhishek Maiti
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Yesid Alvarado
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Naveen Pemmaraju
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Guillermo Montalban Bravo
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Lucia Masarova
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Musa Yilmaz
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Nitin Jain
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Michael Andreeff
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Elias Jabbour
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Guillermo Garcia-Manero
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Steven Kornblau
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Farhad Ravandi
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Marina Y. Konopleva
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX
  • Hagop M. Kantarjian
    Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

書誌事項

公開日
2021-09-01
DOI
  • 10.1200/jco.20.03736
公開者
American Society of Clinical Oncology (ASCO)

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説明

<jats:sec><jats:title>PURPOSE</jats:title><jats:p> Sixty percent of newly diagnosed patients with acute myeloid leukemia (ND-AML) receiving frontline therapy attain a complete response (CR), yet 30%-40% of patients relapse. Relapsed or refractory AML (R/R-AML) remains a particularly adverse population necessitating improved therapeutic options. This phase Ib/II study evaluated the safety and efficacy of fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin combined with the B-cell lymphoma-2 inhibitor venetoclax in ND-AML and R/R-AML. </jats:p></jats:sec><jats:sec><jats:title>MATERIALS AND METHODS</jats:title><jats:p> The phase IB portion (PIB) enrolled patients with R/R-AML using a 3 + 3 dose escalation and de-escalation algorithm for identification of maximum tolerated dose and dose-limiting toxicities. The phase II portion enrolled patients into two arms to evaluate response and time-to-event end points: phase IIA (PIIA): ND-AML and phase IIB (PIIB): R/R-AML. </jats:p></jats:sec><jats:sec><jats:title>RESULTS</jats:title><jats:p> Sixty-eight patients have enrolled to date (PIB, 16; PIIA, 29; PIIB, 23). Median age was 46 years (range, 20-73). Grade 3 and 4 adverse events occurring in ≥ 10% of patients included febrile neutropenia (50%), bacteremia (35%), pneumonia (28%), and sepsis (12%). The overall response rate for PIB, PIIA, and PIIB was 75%, 97%, and 70% with 75%, 90%, and 61%, respectively, achieving a composite CR. Measurable residual disease–negative composite CR was attained in 96% of ND-AML and 69% of R/R-AML patients. After a median follow-up of 12 months, median overall survival (OS) for both PII cohorts was not reached. Fifty-six percent of patients proceeded to allogeneic hematopoietic stem-cell transplantation (ND-AML, 69%; R/R-AML, 46%). In R/R-AML, allogeneic hematopoietic stem-cell transplantation resulted in a significant improvement in OS (median OS, NR; 1-year OS, 87%). One-year survival post-HSCT was 94% in ND-AML and 78% in R/R-AML. </jats:p></jats:sec><jats:sec><jats:title>CONCLUSION</jats:title><jats:p> Fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin + venetoclax represents an effective intensive treatment regimen in ND-AML and R/R-AML patients, associated with deep remissions and a high rate of transition to successful transplantation. </jats:p></jats:sec>

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