Radiation therapy prior to CAR T-cell therapy in lymphoma: impact on patient outcomes

Expert Rev Hematol. 2022 Dec;15(12):1023-1030. doi: 10.1080/17474086.2022.2147919. Epub 2022 Nov 17.

Abstract

Introduction: Anti-CD19 chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment paradigm for patients with refractory or recurrent (R/R) diffuse large B-cell lymphomas (DLBCL). Nonetheless, most patients ultimately progress. The use of bridging or salvage radiotherapy (RT) in combination with CAR T-cell therapy has been proposed as potential strategies to improve patient outcomes, but consensus is currently lacking as to which, if either, approach is effective.

Areas covered: We reviewed the immunologic and molecular mechanisms of resistance and the current retrospective data on patterns-of-failure, clinical risk factors, and treatment outcomes in patients undergoing CAR T-cell therapy, with and without bridging or salvage RT.

Expert opinion: We believe that current basic and clinical evidence supports the use of comprehensive, ablative bridging irradiation (CABI), as opposed to low-dose bridging or salvage radiotherapy, as a promising strategy to improve CAR T-cell therapy outcomes in patients with R/R DLBCL. This potential benefit is likely greatest in patients with high tumor burden and/or localized disease, who are both at elevated risk of local recurrence and can often be safely and comprehensively treated with ablative radiation doses (EQD2 > 39 Gy). Hypothesis-driven clinical trials are needed prospectively assess the impact of radiation on outcomes in patients undergoing CAR T-cell therapy.

Keywords: Bridging radiation; CAR T-cell therapy; DLBCL; patterns of failure; radiation therapy.

Publication types

  • Review

MeSH terms

  • Antigens, CD19
  • Humans
  • Immunotherapy, Adoptive* / adverse effects
  • Lymphoma, Large B-Cell, Diffuse* / drug therapy
  • Lymphoma, Large B-Cell, Diffuse* / radiotherapy
  • Neoplasm Recurrence, Local / drug therapy
  • Retrospective Studies

Substances

  • Antigens, CD19