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Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures
Undifferentiated pleomorphic sarcoma (UPS), an aggressive soft-tissue sarcoma of adults, has been characterized by low tumor mutational burden (TMB) and high copy number alterations. Clinical trials of programmed death-1 (PD-1) blockade in UPS have reported widely varying efficacy. We describe two p...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190056/ https://www.ncbi.nlm.nih.gov/pubmed/34103354 http://dx.doi.org/10.1136/jitc-2021-002345 |
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author | Cheung, Laurene S Chen, Lingling Oke, Teniola F Schaffer, Thomas B Boudadi, Karim Ngo, Jillian T Gross, John McMahon Kemberling, Holly Diaz, Luis A Lipson, Evan Sidhom, John-WIlliam Taube, Janis Anders, Robert Pardoll, Drew M Le, Dung T Meyer, Christian F Llosa, Nicolas |
author_facet | Cheung, Laurene S Chen, Lingling Oke, Teniola F Schaffer, Thomas B Boudadi, Karim Ngo, Jillian T Gross, John McMahon Kemberling, Holly Diaz, Luis A Lipson, Evan Sidhom, John-WIlliam Taube, Janis Anders, Robert Pardoll, Drew M Le, Dung T Meyer, Christian F Llosa, Nicolas |
author_sort | Cheung, Laurene S |
collection | PubMed |
description | Undifferentiated pleomorphic sarcoma (UPS), an aggressive soft-tissue sarcoma of adults, has been characterized by low tumor mutational burden (TMB) and high copy number alterations. Clinical trials of programmed death-1 (PD-1) blockade in UPS have reported widely varying efficacy. We describe two patients with recurrent scalp UPS that experienced clinical benefit from PD-1 blockade. These tumors had high TMB with a UV-induced mutational pattern. Analysis of additional head and neck UPS cases identified five out of seven tumors with high TMB and an ultraviolet (UV) mutational signature. Head and neck UPS tumors also had increased programmed death-ligand 1 (PD-L1) expression and CD8+ T cell infiltration as compared with UPS tumors arising from other sites. In summary, we found that UPS tumors of the head and neck, but not elsewhere, have a PD-L1+, T-cell-inflamed tumor microenvironment and high TMB, suggesting that these tumors represent a distinct genetic subgroup of UPS for which immune checkpoint inhibitor therapy might be effective. |
format | Online Article Text |
id | pubmed-8190056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-81900562021-06-25 Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures Cheung, Laurene S Chen, Lingling Oke, Teniola F Schaffer, Thomas B Boudadi, Karim Ngo, Jillian T Gross, John McMahon Kemberling, Holly Diaz, Luis A Lipson, Evan Sidhom, John-WIlliam Taube, Janis Anders, Robert Pardoll, Drew M Le, Dung T Meyer, Christian F Llosa, Nicolas J Immunother Cancer Case Report Undifferentiated pleomorphic sarcoma (UPS), an aggressive soft-tissue sarcoma of adults, has been characterized by low tumor mutational burden (TMB) and high copy number alterations. Clinical trials of programmed death-1 (PD-1) blockade in UPS have reported widely varying efficacy. We describe two patients with recurrent scalp UPS that experienced clinical benefit from PD-1 blockade. These tumors had high TMB with a UV-induced mutational pattern. Analysis of additional head and neck UPS cases identified five out of seven tumors with high TMB and an ultraviolet (UV) mutational signature. Head and neck UPS tumors also had increased programmed death-ligand 1 (PD-L1) expression and CD8+ T cell infiltration as compared with UPS tumors arising from other sites. In summary, we found that UPS tumors of the head and neck, but not elsewhere, have a PD-L1+, T-cell-inflamed tumor microenvironment and high TMB, suggesting that these tumors represent a distinct genetic subgroup of UPS for which immune checkpoint inhibitor therapy might be effective. BMJ Publishing Group 2021-06-08 /pmc/articles/PMC8190056/ /pubmed/34103354 http://dx.doi.org/10.1136/jitc-2021-002345 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Case Report Cheung, Laurene S Chen, Lingling Oke, Teniola F Schaffer, Thomas B Boudadi, Karim Ngo, Jillian T Gross, John McMahon Kemberling, Holly Diaz, Luis A Lipson, Evan Sidhom, John-WIlliam Taube, Janis Anders, Robert Pardoll, Drew M Le, Dung T Meyer, Christian F Llosa, Nicolas Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title | Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title_full | Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title_fullStr | Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title_full_unstemmed | Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title_short | Anti-PD-1 elicits regression of undifferentiated pleomorphic sarcomas with UV-mutation signatures |
title_sort | anti-pd-1 elicits regression of undifferentiated pleomorphic sarcomas with uv-mutation signatures |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190056/ https://www.ncbi.nlm.nih.gov/pubmed/34103354 http://dx.doi.org/10.1136/jitc-2021-002345 |
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