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Curr Med Sci ; 41(3): 474-481, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34169427

ABSTRACT

Anti-B cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T-cell therapy is effective and well-tolerated for refractory or relapsed multiple myeloma (RRMM). The purpose of the present study was to analyze efficacy in RRMM patients with renal impairment treated by anti-BCMA CAR-T cell therapy. A total of 59 RRMM patients were selected, and divided into impaired renal function (IRF) group [baseline estimated glomerular filtration rate (eGFR) < 90 mL/min/1.73 m2 (n=18)] and normal renal function (NRF) group (baseline eGFR ≥ 90 mL/min/1.73 m2, n=41). For patients with IRF, eGFR at the 6th month post-CAR-T cells infusion was significantly higher than the baseline (P<0.05). The multivariate analysis showed that light chain type and beta-2 micro-globulin (beta-2M) were associated factors with the decrease of serum creatinine. Median progression-free survival (PFS) in the NRF group and IRF group was 266 days and 181 days respectively. Overall survival (OS) in the NRF group and IRF group was 877 days and 238 days respectively. There was no significant difference in the objective response rate (ORR) between the IRF group and the NRF group. It is suggested that CAR-T cells therapy could improve the renal function during the treatment of RRMM. The renal function could be more significantly improved in RRMM patients with light chain type than with other types.


Subject(s)
B-Cell Maturation Antigen/genetics , Immunotherapy, Adoptive , Kidney Diseases/therapy , Multiple Myeloma/therapy , Adult , B-Cell Maturation Antigen/antagonists & inhibitors , Cell- and Tissue-Based Therapy/trends , Female , Gene Expression Regulation, Neoplastic/drug effects , Humans , Kidney/drug effects , Kidney/pathology , Kidney Diseases/complications , Kidney Diseases/genetics , Kidney Diseases/pathology , Male , Middle Aged , Multiple Myeloma/complications , Multiple Myeloma/genetics , Multiple Myeloma/pathology , Receptors, Chimeric Antigen/genetics , Receptors, Chimeric Antigen/therapeutic use
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