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Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma
BACKGROUND: Checkpoint inhibitors (CPIs) are thought to be effective against cutaneous melanoma in part because of the large burden of somatic mutations (neoantigens) generated from exposure to ultraviolet radiation. However, rare melanoma subtypes arising from acral skin, mucosal surfaces, and the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103823/ https://www.ncbi.nlm.nih.gov/pubmed/32209601 http://dx.doi.org/10.1136/jitc-2019-000341 |
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author | Klemen, Nicholas D. Wang, Melinda Rubinstein, Jill C. Olino, Kelly Clune, James Ariyan, Stephan Cha, Charles Weiss, Sarah A. Kluger, Harriet M. Sznol, Mario |
author_facet | Klemen, Nicholas D. Wang, Melinda Rubinstein, Jill C. Olino, Kelly Clune, James Ariyan, Stephan Cha, Charles Weiss, Sarah A. Kluger, Harriet M. Sznol, Mario |
author_sort | Klemen, Nicholas D. |
collection | PubMed |
description | BACKGROUND: Checkpoint inhibitors (CPIs) are thought to be effective against cutaneous melanoma in part because of the large burden of somatic mutations (neoantigens) generated from exposure to ultraviolet radiation. However, rare melanoma subtypes arising from acral skin, mucosal surfaces, and the uveal tract are largely sun-shielded. Genomic studies show these sun-shielded melanomas have a paucity of neoantigens and unique biology; they are thought to be largely resistant to immunotherapy. It has not been definitively shown that CPI improves survival in metastatic sun-shielded melanoma. METHODS: We reviewed a single institutional experience using antibodies against CTLA-4, PD-1 and/or PD-L1 to treat patients with metastatic melanoma. Primary tumor histology was categorized as cutaneous, unknown, acral, mucosal, or uveal. We studied demographic data, treatment characteristics, and overall survival (OS) after CPI. RESULTS: We treated 428 patients with metastatic melanoma from 2007 to 2019. Primary tumors were cutaneous in 283 (66%), unknown in 55 (13%), acral in 22 (5%), mucosal in 38 (9%), and uveal in 30 (7%). Patients with metastatic disease from cutaneous primary tumors had median OS after CPI of 45 months compared with 17 months for acral (p=0.047), 18 months for mucosal (p=0.003), and 12 months for uveal (p<0.001). For all patients with sun-shielded melanoma (n=90), first treatment with anti-PD-1 or anti-PD-L1 was followed by a median OS of 9 months compared with 18 months after anti-CTLA-4 (p=0.010) and 20 months after combination therapy (p=0.003). There were 21 patients who achieved actual 3-year survival; 20 received both anti-CTLA-4 and anti-PD-1, either sequentially or in combination. Over 80% of 3-year survivors with progressive disease were treated with local therapy after CPI. CONCLUSIONS: Long survival in patients with metastatic melanoma from acral, mucosal, and uveal primary tumors was associated with receipt of both anti-CTLA-4 and anti-PD-1 antibodies. Complete responses were rare, and local therapy was frequently employed to control disease progression. While sun-shielded melanomas exhibit worse outcomes after CPI than cutaneous melanomas, with an aggressive multidisciplinary approach, 5-year survival is still possible for 25%–32% of these patients. |
format | Online Article Text |
id | pubmed-7103823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-71038232020-03-31 Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma Klemen, Nicholas D. Wang, Melinda Rubinstein, Jill C. Olino, Kelly Clune, James Ariyan, Stephan Cha, Charles Weiss, Sarah A. Kluger, Harriet M. Sznol, Mario J Immunother Cancer Short Report BACKGROUND: Checkpoint inhibitors (CPIs) are thought to be effective against cutaneous melanoma in part because of the large burden of somatic mutations (neoantigens) generated from exposure to ultraviolet radiation. However, rare melanoma subtypes arising from acral skin, mucosal surfaces, and the uveal tract are largely sun-shielded. Genomic studies show these sun-shielded melanomas have a paucity of neoantigens and unique biology; they are thought to be largely resistant to immunotherapy. It has not been definitively shown that CPI improves survival in metastatic sun-shielded melanoma. METHODS: We reviewed a single institutional experience using antibodies against CTLA-4, PD-1 and/or PD-L1 to treat patients with metastatic melanoma. Primary tumor histology was categorized as cutaneous, unknown, acral, mucosal, or uveal. We studied demographic data, treatment characteristics, and overall survival (OS) after CPI. RESULTS: We treated 428 patients with metastatic melanoma from 2007 to 2019. Primary tumors were cutaneous in 283 (66%), unknown in 55 (13%), acral in 22 (5%), mucosal in 38 (9%), and uveal in 30 (7%). Patients with metastatic disease from cutaneous primary tumors had median OS after CPI of 45 months compared with 17 months for acral (p=0.047), 18 months for mucosal (p=0.003), and 12 months for uveal (p<0.001). For all patients with sun-shielded melanoma (n=90), first treatment with anti-PD-1 or anti-PD-L1 was followed by a median OS of 9 months compared with 18 months after anti-CTLA-4 (p=0.010) and 20 months after combination therapy (p=0.003). There were 21 patients who achieved actual 3-year survival; 20 received both anti-CTLA-4 and anti-PD-1, either sequentially or in combination. Over 80% of 3-year survivors with progressive disease were treated with local therapy after CPI. CONCLUSIONS: Long survival in patients with metastatic melanoma from acral, mucosal, and uveal primary tumors was associated with receipt of both anti-CTLA-4 and anti-PD-1 antibodies. Complete responses were rare, and local therapy was frequently employed to control disease progression. While sun-shielded melanomas exhibit worse outcomes after CPI than cutaneous melanomas, with an aggressive multidisciplinary approach, 5-year survival is still possible for 25%–32% of these patients. BMJ Publishing Group 2020-03-24 /pmc/articles/PMC7103823/ /pubmed/32209601 http://dx.doi.org/10.1136/jitc-2019-000341 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://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/. |
spellingShingle | Short Report Klemen, Nicholas D. Wang, Melinda Rubinstein, Jill C. Olino, Kelly Clune, James Ariyan, Stephan Cha, Charles Weiss, Sarah A. Kluger, Harriet M. Sznol, Mario Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title | Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title_full | Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title_fullStr | Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title_full_unstemmed | Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title_short | Survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
title_sort | survival after checkpoint inhibitors for metastatic acral, mucosal and uveal melanoma |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103823/ https://www.ncbi.nlm.nih.gov/pubmed/32209601 http://dx.doi.org/10.1136/jitc-2019-000341 |
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