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Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma

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 sa...

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Autores principales: Samur, Mehmet Kemal, Fulciniti, Mariateresa, Aktas Samur, Anil, Bazarbachi, Abdul Hamid, Tai, Yu-Tzu, Prabhala, Rao, Alonso, Alejandro, Sperling, Adam S., Campbell, Timothy, Petrocca, Fabio, Hege, Kristen, Kaiser, Shari, Loiseau, Hervé Avet, Anderson, Kenneth C., Munshi, Nikhil C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870932/
https://www.ncbi.nlm.nih.gov/pubmed/33558511
http://dx.doi.org/10.1038/s41467-021-21177-5
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author Samur, Mehmet Kemal
Fulciniti, Mariateresa
Aktas Samur, Anil
Bazarbachi, Abdul Hamid
Tai, Yu-Tzu
Prabhala, Rao
Alonso, Alejandro
Sperling, Adam S.
Campbell, Timothy
Petrocca, Fabio
Hege, Kristen
Kaiser, Shari
Loiseau, Hervé Avet
Anderson, Kenneth C.
Munshi, Nikhil C.
author_facet Samur, Mehmet Kemal
Fulciniti, Mariateresa
Aktas Samur, Anil
Bazarbachi, Abdul Hamid
Tai, Yu-Tzu
Prabhala, Rao
Alonso, Alejandro
Sperling, Adam S.
Campbell, Timothy
Petrocca, Fabio
Hege, Kristen
Kaiser, Shari
Loiseau, Hervé Avet
Anderson, Kenneth C.
Munshi, Nikhil C.
author_sort Samur, Mehmet Kemal
collection PubMed
description 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.
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spelling pubmed-78709322021-02-11 Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma Samur, Mehmet Kemal Fulciniti, Mariateresa Aktas Samur, Anil Bazarbachi, Abdul Hamid Tai, Yu-Tzu Prabhala, Rao Alonso, Alejandro Sperling, Adam S. Campbell, Timothy Petrocca, Fabio Hege, Kristen Kaiser, Shari Loiseau, Hervé Avet Anderson, Kenneth C. Munshi, Nikhil C. Nat Commun Article 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. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870932/ /pubmed/33558511 http://dx.doi.org/10.1038/s41467-021-21177-5 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Samur, Mehmet Kemal
Fulciniti, Mariateresa
Aktas Samur, Anil
Bazarbachi, Abdul Hamid
Tai, Yu-Tzu
Prabhala, Rao
Alonso, Alejandro
Sperling, Adam S.
Campbell, Timothy
Petrocca, Fabio
Hege, Kristen
Kaiser, Shari
Loiseau, Hervé Avet
Anderson, Kenneth C.
Munshi, Nikhil C.
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title_full Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title_fullStr Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title_full_unstemmed Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title_short Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma
title_sort biallelic loss of bcma as a resistance mechanism to car t cell therapy in a patient with multiple myeloma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870932/
https://www.ncbi.nlm.nih.gov/pubmed/33558511
http://dx.doi.org/10.1038/s41467-021-21177-5
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