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Four-year follow-up of LCAR-B38M in relapsed or refractory multiple myeloma: a phase 1, single-arm, open-label, multicenter study in China (LEGEND-2)

  • Wan Hong Zhao
  • , Bai Yan Wang
  • , Li Juan Chen
  • , Wei Jun Fu
  • , Jie Xu
  • , Jie Liu
  • , Shi Wei Jin
  • , Yin Xia Chen
  • , Xing Mei Cao
  • , Yun Yang
  • , Yi Lin Zhang
  • , Fang Xia Wang
  • , Peng Yu Zhang
  • , Bo Lei
  • , Liu Fang Gu
  • , Jian Li Wang
  • , Hui Zhang
  • , Ju Bai
  • , Yan Xu
  • , Han Zhu
  • Juan Du, Hua Jiang, Xiao Hu Fan, Jian Yong Li, Jian Hou, Zhu Chen, Wang Gang Zhang, Jian Qing Mi, Sai Juan Chen, Ai Li He
  • The Second Affiliated Hospital of Xi'an Jiaotong University
  • The First Affiliated Hospital with Nanjing Medical University
  • Navy Medical University
  • Tongji University
  • Shanghai Jiao Tong University
  • Nanjing Legend Biotech Inc.

Research output: Contribution to journalArticlepeer-review

126 Scopus citations

Abstract

Background: LCAR-B38M is a chimeric antigen receptor T cell product with two binding domains targeting B cell maturation antigen. Our previous reports showed a remarkable efficacy of LCAR-B38M in patients with relapsed/refractory multiple myeloma (RRMM) at a median follow-up of 2 years. Here, we report long-term safety and efficacy data from a median follow-up of 4 years. Methods: LEGEND-2 was a phase 1, single-arm, open-label study conducted in four registered sites in China. Seventy-four participants with RRMM received LCAR-B38M treatment. Lymphodepletion was performed using cyclophosphamide or cyclophosphamide plus fludarabine. LCAR-B38M, at a median dose of 0.513 × 106 cells/kg, was intravenously administered either in three split infusions or in a single infusion. The primary objective was the safety of LCAR-B38M, and the secondary objective was efficacy. Results: As of May 25, 2021, the median follow-up was 47.8 months. All patients experienced ≥ 1 adverse events (AEs). Grade ≥ 3 AEs were observed in 45/74 (60.8%) patients. Cytokine release syndrome (CRS) occurred in 68/74 (91.9%) cases; 7 (9.5%) had grade ≥ 3 CRS. One patient experienced grade 1 central nervous system toxicity. The overall response rate was 87.8%. Fifty-four out of 74 (73.0%) patients achieved complete response. The median progression-free survival was 18.0 months, and the median overall survival for all patients was not reached. The median duration of response was 23.3 months. Four patients experienced viral infection more than 6 months post-infusion, and four patients developed second primary non-hematological malignancies at a median time of 11.5 months post-CAR-T cell transfer. Conclusions: The 4-year follow-up data of LCAR-B38M therapy demonstrated a favorable long-term safety profile and a durable response in patients with RRMM. Trial registration Clinicaltrials.gov NCT03090659 (retrospectively registered on March 27, 2017); ChiCTR-ONH-17012285.

Original languageEnglish
Article number86
JournalJournal of Hematology and Oncology
Volume15
Issue number1
DOIs
StatePublished - Dec 2022
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • B cell maturation antigen
  • Chimeric antigen receptor therapy
  • Efficacy
  • Multiple myeloma
  • Safety

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