[CAR-T cells in acute lymphoblastic leukemias: What's new?]

Bull Cancer. 2020 Feb;107(2):234-243. doi: 10.1016/j.bulcan.2020.01.009. Epub 2020 Feb 5.
[Article in French]

Abstract

The approval of tisagenlecleucel in B-lineage acute lymphoblastic leukemias in 2017 in the USA and in 2018 in Europe not only opened new hopes but forced to rethink the hospital organizations around this innovation. Indeed, if these treatments are very effective in the short term, the complex logistics required imply high quality inter-center and intra-center collaboration. Hematology, intensive care unit, apheresis, neurology, cell therapy and biology laboratories, and radiology services must therefore act in a coordinated manner. A specialized monitoring for the mid and long term must also be implemented. Many questions remain concerning the profile of eligible patients, the short and long-term safety, the longer-term efficacy, improving the persistence of CAR-T cells, controlling the risk of tumor escape, the use of allogenic CAR-T cells, or the application of this concept to T-cell ALL. The precise evaluation of the involved costs and the cost-effectiveness of these therapies will also be the subject of future studies.

Keywords: Acute lymphoblastique Leukemia; CAR-T cells; Leucémie aiguë lymphoblastique; Tisagenlecleucel; « CAR-T cells ».

Publication types

  • Review

MeSH terms

  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Immunotherapy, Adoptive / methods*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / immunology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / therapy*
  • Prognosis
  • Receptors, Antigen, T-Cell / therapeutic use
  • Receptors, Chimeric Antigen / therapeutic use*
  • Recurrence
  • T-Lymphocytes / drug effects

Substances

  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen
  • tisagenlecleucel