[Prevention and management of infections in patients undergoing CAR T-cell therapy: Recommendations of the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)]

Bull Cancer. 2021 Dec;108(12S):S90-S97. doi: 10.1016/j.bulcan.2021.11.001. Epub 2021 Dec 6.
[Article in French]

Abstract

Infections occurring after CAR T-cells are a common complication. At the acute phase of treatment following CAR T-cell infusion, the exact incidence of infections is unknown given the overlapping symptoms with cytokine release syndrome. The risk factors for infection include the malignant underlying disease and its multiple treatments, and an immunosuppressive state induced by CAR-T cells themselves and the treatment of their complications. During the twelfth edition of practice harmonization workshops of the Francophone society of bone marrow transplantation and cellular therapy (SFGM-TC), a working group focused its work on the management of post-CAR infectious complications. In this review we discuss anti-infection prophylaxis and vaccination of patients undergoing CAR T-cell therapy as well as a special chapter for the specific case of COVID-19. These recommendations apply to commercial CAR-T cells, in order to guide strategies for the management and prevention of infectious complications associated with this new therapeutic approach.

Keywords: CAR T-cell therapy; CAR-T cells; Infections; Prophylaxie; Prophylaxis; Vaccination.

Publication types

  • Practice Guideline
  • Review

MeSH terms

  • Bacterial Infections / prevention & control*
  • Bone Marrow Transplantation
  • COVID-19 / prevention & control
  • Cell Transplantation
  • Cytokine Release Syndrome
  • Humans
  • Immunization
  • Immunocompromised Host
  • Immunoglobulins / therapeutic use
  • Immunotherapy, Adoptive* / adverse effects
  • Mycoses / prevention & control*
  • Neoplasms / complications
  • Neoplasms / therapy
  • Pneumocystis
  • Receptors, Chimeric Antigen / therapeutic use*
  • Risk Factors
  • Virus Diseases / prevention & control*

Substances

  • Immunoglobulins
  • Receptors, Chimeric Antigen