| Literature DB >> 33558511 |
Mehmet Kemal Samur1,2,3, Mariateresa Fulciniti4, Anil Aktas Samur5,6, Abdul Hamid Bazarbachi4,7, Yu-Tzu Tai4, Rao Prabhala4,8, Alejandro Alonso4, Adam S Sperling4, Timothy Campbell9, Fabio Petrocca10, Kristen Hege9, Shari Kaiser11, Hervé Avet Loiseau12, Kenneth C Anderson4, Nikhil C Munshi13,14.
Abstract
BCMA targeting chimeric antigen receptor (CAR) T cell therapy has shown deep and durable responses in multiple myeloma. However, relapse following therapy is frequently observed, and mechanisms of resistance remain ill-defined. Here, we perform single cell genomic characterization of longitudinal samples from a patient who relapsed after initial CAR T cell treatment with lack of response to retreatment. We report selection, following initial CAR T cell infusion, of a clone with biallelic loss of BCMA acquired by deletion of one allele and a mutation that creates an early stop codon on the second allele. This loss leads to lack of CAR T cell proliferation following the second infusion and is reflected by lack of soluble BCMA in patient serum. Our analysis suggests the need for careful detection of BCMA gene alterations in multiple myeloma cells from relapse following CAR T cell therapy.Entities:
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Year: 2021 PMID: 33558511 PMCID: PMC7870932 DOI: 10.1038/s41467-021-21177-5
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919