A combination of humanized anti-BCMA and murine anti-CD38 CAR-T cell therapy in patients with relapsed or refractory multiple myeloma

Leuk Lymphoma. 2022 Jun;63(6):1418-1427. doi: 10.1080/10428194.2022.2030476. Epub 2022 Feb 1.

Abstract

Chimeric antigen receptor T (CAR-T) cells are a promising approach in hematopoietic malignancies. We evaluated the safety and efficacy of a combination of humanized anti-BCMA and murine anti-CD38 CAR-T cell therapy in patients with relapsed or refractory multiple myeloma (R/RMM). Twenty-two R/RMM patients, with a median age of 56 years and a median number of previous therapies of 8, were included in the study. Both CAR-T cells infusion doses were 2.0 × 106/kg. The overall response rate (ORR) was 90.9%, with 12 patients (54.5%) achieving a strict complete response/complete response (sCR/CR). The 24-month overall survival (OS) rate was 56.6%, and the progression-free survival (PFS) rate was 48.7%. Cytokine release syndrome (CRS) of grades 1-2 occurred in 16 patients (72.7%) and of grade ≥3 in six patients (27.3%). Immune effector cell-associated neurotoxic syndrome (ICANS) of grades 1-2 occurred in three patients (13.6%). The combination therapy is potential in R/RMM patients.Trial registration: The patients were enrolled in clinical trials registered as ChiCTR1800017051.

Keywords: Anti-BCMA CAR-T; anti-CD38 CAR-T; combination therapy; efficacy; safety.

MeSH terms

  • Animals
  • B-Cell Maturation Antigen / agonists
  • Cell- and Tissue-Based Therapy
  • Clinical Trials as Topic
  • Combined Modality Therapy / adverse effects
  • Humans
  • Immunotherapy, Adoptive*
  • Mice
  • Middle Aged
  • Multiple Myeloma* / drug therapy
  • Receptors, Chimeric Antigen* / therapeutic use

Substances

  • B-Cell Maturation Antigen
  • Receptors, Chimeric Antigen

Associated data

  • ChiCTR/ChiCTR1800017051