Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma.
Mehmet Kemal SamurMaria Teresa FulcinitiAnil Aktas SamurAbdul-Hamid BazarbachiYu-Tzu TaiRao PrabhalaAlejandro AlonsoAdam S SperlingTimothy CampbellFabio PetroccaKristen HegeShari KaiserHervé Avet LoiseauKenneth C AndersonNikhil C MunshiPublished in: Nature communications (2021)
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.
Keyphrases
- cell therapy
- multiple myeloma
- stem cells
- mesenchymal stem cells
- case report
- cell proliferation
- single cell
- low dose
- intellectual disability
- copy number
- acute lymphoblastic leukemia
- high throughput
- acute myeloid leukemia
- free survival
- diffuse large b cell lymphoma
- bone marrow
- cancer therapy
- rna seq
- dna methylation
- transcription factor
- hodgkin lymphoma
- signaling pathway
- cell cycle
- quantum dots
- smoking cessation
- genome wide identification