[Treatment stratification by fitness for chemotherapy in acute myeloid leukemia]

Rinsho Ketsueki. 2022;63(6):667-677. doi: 10.11406/rinketsu.63.667.
[Article in Japanese]

Abstract

Acute myelogenous leukemia (AML) is a hematopoietic malignancy that is characterized by clonal autonomous proliferation of myeloid cells with impaired differentiation and maturation. Recent advances in next-generation sequencing technology have elucidated the pathogenesis of AML at the genetic level. Furthermore, the molecular targeted therapy to efficiently eradicate leukemic cells has been rapidly expanding since 2017. In Japan, gilteritinib and quizartinib, which target FMS-like tyrosine kinase 3, and venetoclax, which targets B-cell lymphoma 2, have finally become available after resolving the drug launch lag between Japan and the United States. The combination of venetoclax and azacitidine, which was simultaneously approved with venetoclax for AML, is expected to be more effective than conventional therapy in patients who are ineligible for transplantation. Herein, we review the National Comprehensive Cancer Network guidelines for intensive chemotherapy in Japan and the United States and discuss the future of AML treatment, including the development of novel agents.

Keywords: Acute myelogenous leukemia; Fitness; Novel agents; Treatment.

Publication types

  • Review

MeSH terms

  • Azacitidine / therapeutic use
  • Bridged Bicyclo Compounds, Heterocyclic / therapeutic use
  • Humans
  • Leukemia, Myeloid, Acute* / drug therapy
  • Leukemia, Myeloid, Acute* / genetics
  • Protein Kinase Inhibitors* / therapeutic use
  • Proto-Oncogene Proteins c-bcl-2
  • Sulfonamides
  • United States
  • fms-Like Tyrosine Kinase 3

Substances

  • Bridged Bicyclo Compounds, Heterocyclic
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Sulfonamides
  • fms-Like Tyrosine Kinase 3
  • Azacitidine
  • venetoclax