[Hairy cell leukemia: What are the best treatment options for relapsed or refractory patients?]

Bull Cancer. 2021 Jul-Aug;108(7-8):771-778. doi: 10.1016/j.bulcan.2021.03.011. Epub 2021 May 20.
[Article in French]

Abstract

Hairy cell leukemia is a rare form of leukemia: three hundred new cases are diagnosed each year in France. The diagnosis is based on: (1) morphological examination of the blood and bone marrow smear, (2) analysis by flow cytometry of hairy cells, which express three or the four following markers: CD11c, CD25, CD103 and CD123, (3) identification of the BRAFV600E mutation, a true molecular marker of the disease. The management of treatment has evolved considerably in recent years. As of today, the purine analogues remain the standard treatment in the first line. Relapses are however observed in about 40% of cases. In the event of a first relapse, the preferred option is treatment with immunochemotherapy i.e. a combination of cladribine plus rituximab. Subsequent relapses are treated with moxetumomab pasudotox or BRAF inhibitors which provide indisputable benefits if third-line treatment is required. We will discuss in patients with relapsed/refractory hairy cell leukemia the needs for personalized medicine and the advantages and disadvantages of each treatment modality. The good prognosis for LT requires treatments that are not immunosuppressive, non-myelotoxic, and do not increase the risk of secondary cancers.

Keywords: Hairy cell leukemia; Leucémie à tricholeucocytes; Moxetuomab pasudotox; Traitement; Treatment; Vemurafebnib.

Publication types

  • Review

MeSH terms

  • Antigens, Neoplasm / analysis
  • Antineoplastic Agents, Immunological / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bacterial Toxins / therapeutic use
  • Biomarkers, Tumor / analysis
  • Cladribine / therapeutic use
  • Drug Resistance, Neoplasm
  • Exotoxins / therapeutic use
  • Humans
  • Immunotherapy / methods
  • Leukemia, Hairy Cell / diagnosis
  • Leukemia, Hairy Cell / therapy*
  • Mansonelliasis
  • Mutation
  • Neoplasms, Second Primary / prevention & control
  • Pentostatin / therapeutic use
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf / genetics
  • Rare Diseases / diagnosis
  • Rare Diseases / therapy*
  • Recurrence
  • Rituximab / therapeutic use

Substances

  • Antigens, Neoplasm
  • Antineoplastic Agents, Immunological
  • Bacterial Toxins
  • Biomarkers, Tumor
  • Exotoxins
  • immunotoxin HA22
  • Pentostatin
  • Cladribine
  • Rituximab
  • Proto-Oncogene Proteins B-raf