Fludarabine, cytarabine, and idarubicin with or without venetoclax in patients with relapsed/refractory acute myeloid leukemia

Haematologica. 2024 Jan 1;109(1):72-83. doi: 10.3324/haematol.2023.282912.

Abstract

Treatment options for relapsed and refractory acute myeloid leukemia patients (R/R AML) are limited. This retrospective cohort study compares safety and efficacy of fludarabine, cytarabine, and idarubicin (FLA-IDA) without or with venetoclax (FLAVIDA) in patients with R/R AML. Thirty-seven and 81 patients received one course FLA-IDA with or without a 7-day course of venetoclax, respectively. The overall response rate (ORR) was significantly higher in FLAVIDA compared to FLAIDA- treated patients (78% vs. 47%; P=0.001), while measurable residual disease was negative at a similar proportion in responding patients (50% vs. 57%), respectively. Eighty-one percent and 79% of patients proceeded to allogeneic hematopoietic cell transplantation or donor lymphocyte infusion after FLAVIDA and FLA-IDA, respectively. Event-free and overall survival were similar in FLAVIDA- and FLA-IDA-treated patients. Refractory patients could be salvaged more successfully after FLA-IDA compared to FLAVIDA pretreatment. Neutrophil and platelet recovery times were similar in the venetoclax and the control group. In conclusion, short-term venetoclax in combination with FLA-IDA represents an effective treatment regimen in R/R AML identifying chemosensitive patients rapidly and inducing measurable residual disease-negative remission in a high proportion of R/R AML patients.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Cytarabine
  • Granulocyte Colony-Stimulating Factor
  • Humans
  • Idarubicin* / therapeutic use
  • Leukemia, Myeloid, Acute* / drug therapy
  • Retrospective Studies
  • Vidarabine

Substances

  • Idarubicin
  • Cytarabine
  • venetoclax
  • fludarabine
  • Granulocyte Colony-Stimulating Factor
  • Vidarabine

Grants and funding

Funding: This study was supported by grants HE 5240/6-1, HE 5240/6-2 to MH from DFG, an ERC grant to MH from the European Union’s Horizon 2020 research and innovation programme (no. 638035), grant 16 R/2021 to MH from DJCLS, and grant 70114189 to MH from Deutsche Krebshilfe. RS received a grant from PRACTIS.