AI Article Synopsis

  • The "7+3" regimen has been the standard AML treatment for many years, but new medications have emerged that present additional options for patients.
  • Current strategies for AML treatment are tailored to individual patient needs, taking into account factors like age, fitness, and specific genetic mutations.
  • For older or less fit patients, a combination of azacytidine and Venetoclax shows promise, while new therapies for IDH1 and IDH2 mutations are also being explored despite not yet being EMA-approved.

Article Abstract

Background: While the "7+3" regimen of cytarabine + anthracycline has been the backbone of acute myeloid leukemia (AML) treatment for four decades, several novel drugs have been approved in the past five years. Despite these promising novel therapeutic options, treatment of AML remains challenging, given the biologically heterogenous character of the disease.

Aim: This review provides an update on novel treatment strategies for AML.

Material And Methods: This article is based on the current European LeukemiaNet (ELN) recommendations and the DGHO «Onkopedia» guideline on AML treatment.

Results And Conclusion: The treatment algorithm is based on patient-related and disease-specific factors, such as patient age and fitness as well as AML molecular profile. Younger patients considered fit for intensive chemotherapy receive 1-2 courses of induction therapy ("7+3" regimen, eg. cytarabine/daunorubicin, or CPX-351 for patients with myelodysplasia-related AML or therapy-related AML). For CD33+ patients or those with evidence of an mutation "7+3" in combination with Gemtuzumab-Ozogamicin (GO) or Midostaurin is recommended, respectively. For consolidation, patients receive either high-dose chemotherapy (± GO/± Midostaurin) or undergo allogeneic hematopoietic cell transplantation (HCT), based on ELN risk stratification. In some cases, maintenance therapy with oral azacytidine or inhibitor is indicated. Patients experiencing relapse should receive chemotherapy-based re-induction therapy or, in case of an mutation, Gilteritinib and subsequently undergo allogeneic HCT. For older patients or those considered unfit for intensive therapy, azacytidine in combination with Venetoclax is a promising novel treatment strategy. Although not yet approved by the European Medical Agency (EMA), for patients with IDH1 or mutations treatment with the IDH1 and IDH2 inhibitors Ivosidenib and Enasidenib should be considered.

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Source
http://dx.doi.org/10.1055/a-1873-4753DOI Listing

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