Optimal Post-Remission Consolidation Therapy in Patients with AML

Acta Haematol. 2024;147(2):147-158. doi: 10.1159/000535457. Epub 2023 Nov 26.

Abstract

Background: Despite recent advances, 40-85% of patients with acute myeloid leukaemia (AML) achieve complete remission after intensive chemotherapy. However, without optimal treatment after remission, the risk of relapse remains high.

Summary: A variable number of consolidation cycles consisting of intermediate doses of cytarabine are the most commonly used regimens in low-intermediate-risk AML, while patients at higher risk of relapse should consolidate response by proceeding to HSCT. Different post-consolidation (maintenance therapies) have demonstrated their benefit in prolonging relapse-free survival, and others are still under investigation. Careful consideration should be given to which patients benefit most from each of these interventions, considering that the risk of relapse is dynamic.

Key messages: Patients consolidated with chemotherapy should receive either 2 courses of HDAC or no more than 3-4 cycles of IDAC with dose reduction in patients over 60 years. Patients with mutated FLT3 AML benefit from post-consolidation maintenance with FLT3 inhibitors, and selected patients not fit for adequate consolidation may benefit from CC-468 maintenance. Patients at higher risk of relapse should proceed to allogeneic SCT as soon as possible, opting for a more intensive conditioning in patients younger than 55 years. However, autologous HSCT may still have role in favourable-risk MRD-negative AML. Multiple treatment options targeting MRD are emerging, either as definitive treatment or as a bridge to allogeneic transplantation, and are likely to become increasingly relevant.

Keywords: Acute myeloid leukaemia; Consolidation; Haematopoietic stem cell transplantation; Maintenance; Measurable residual disease.

Publication types

  • Review

MeSH terms

  • Consolidation Chemotherapy
  • Cytarabine / therapeutic use
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Leukemia, Myeloid, Acute* / drug therapy
  • Neoplasm Recurrence, Local / drug therapy
  • Recurrence
  • Remission Induction

Substances

  • Cytarabine

Grants and funding

The authors received no financial support for the research, authorship, or publication of this article.