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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-7870932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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