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Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial
BACKGROUND: In the CheckMate-141 trial, nivolumab conferred a survival benefit in patients with recurrent or metastatic refractory squamous cell carcinoma (SCC) head and neck cancer (HNC). Here, we examined the efficacy of nivolumab in patients with histological subtypes or primary sites of HNC not...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280058/ https://www.ncbi.nlm.nih.gov/pubmed/32581587 http://dx.doi.org/10.2147/CMAR.S249393 |
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author | Sato, Yasuyoshi Fukuda, Naoki Wang, Xiaofei Urasaki, Tetsuya Ohmoto, Akihiro Nakano, Kenji Yunokawa, Mayu Ono, Makiko Sato, Yukiko Mitani, Hiroki Tomomatsu, Junichi Takahashi, Shunji |
author_facet | Sato, Yasuyoshi Fukuda, Naoki Wang, Xiaofei Urasaki, Tetsuya Ohmoto, Akihiro Nakano, Kenji Yunokawa, Mayu Ono, Makiko Sato, Yukiko Mitani, Hiroki Tomomatsu, Junichi Takahashi, Shunji |
author_sort | Sato, Yasuyoshi |
collection | PubMed |
description | BACKGROUND: In the CheckMate-141 trial, nivolumab conferred a survival benefit in patients with recurrent or metastatic refractory squamous cell carcinoma (SCC) head and neck cancer (HNC). Here, we examined the efficacy of nivolumab in patients with histological subtypes or primary sites of HNC not included in the CheckMate-141 trial. METHODS: This was a retrospective analysis of data collected prospectively from 97 patients who were treated with nivolumab for recurrent or metastatic HNC at our institution. The patients were assigned to three groups based on HNC primary site: 1) oral cavity, pharynx, and larynx, which were included in CheckMate-141 (n = 68), 2) nasopharynx (excluded in CheckMate-141, n = 7) and 3) other primary sites excluded in CheckMate-141 (n = 22) and assigned to two groups according to histological subtype: 1) SCC (included in CheckMate-141, n = 83) and 2) non-SCC (all sites excluded in CheckMate-141, n = 14). Survival outcomes and nivolumab treatment response were compared between the primary site and histological subgroups. RESULTS: The median number of nivolumab treatments was 7 cycles (range, 1–53 cycles) and the median follow-up time was 9.1 months (range, 0.66–33.0 months). There were no significant differences in response rates between the three primary site subgroups (CheckMate-141 sites 22%, nasopharynx 43%, others 18%; p=0) or the two histological subtype subgroups (SCC 25%, non-SCC 7%, p=0). Similarly, overall survival and progression-free survival were comparable for patients stratified by primary site or histological subtype. CONCLUSION: No significant difference in response rates or survival outcomes was detected between nivolumab-treated HNC patients with primary sites and histological subtypes that were included versus excluded in the CheckMate-141 trial. These data provide a potential rationale for nivolumab therapy for all HNC patients in clinical practice. |
format | Online Article Text |
id | pubmed-7280058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-72800582020-06-23 Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial Sato, Yasuyoshi Fukuda, Naoki Wang, Xiaofei Urasaki, Tetsuya Ohmoto, Akihiro Nakano, Kenji Yunokawa, Mayu Ono, Makiko Sato, Yukiko Mitani, Hiroki Tomomatsu, Junichi Takahashi, Shunji Cancer Manag Res Original Research BACKGROUND: In the CheckMate-141 trial, nivolumab conferred a survival benefit in patients with recurrent or metastatic refractory squamous cell carcinoma (SCC) head and neck cancer (HNC). Here, we examined the efficacy of nivolumab in patients with histological subtypes or primary sites of HNC not included in the CheckMate-141 trial. METHODS: This was a retrospective analysis of data collected prospectively from 97 patients who were treated with nivolumab for recurrent or metastatic HNC at our institution. The patients were assigned to three groups based on HNC primary site: 1) oral cavity, pharynx, and larynx, which were included in CheckMate-141 (n = 68), 2) nasopharynx (excluded in CheckMate-141, n = 7) and 3) other primary sites excluded in CheckMate-141 (n = 22) and assigned to two groups according to histological subtype: 1) SCC (included in CheckMate-141, n = 83) and 2) non-SCC (all sites excluded in CheckMate-141, n = 14). Survival outcomes and nivolumab treatment response were compared between the primary site and histological subgroups. RESULTS: The median number of nivolumab treatments was 7 cycles (range, 1–53 cycles) and the median follow-up time was 9.1 months (range, 0.66–33.0 months). There were no significant differences in response rates between the three primary site subgroups (CheckMate-141 sites 22%, nasopharynx 43%, others 18%; p=0) or the two histological subtype subgroups (SCC 25%, non-SCC 7%, p=0). Similarly, overall survival and progression-free survival were comparable for patients stratified by primary site or histological subtype. CONCLUSION: No significant difference in response rates or survival outcomes was detected between nivolumab-treated HNC patients with primary sites and histological subtypes that were included versus excluded in the CheckMate-141 trial. These data provide a potential rationale for nivolumab therapy for all HNC patients in clinical practice. Dove 2020-06-03 /pmc/articles/PMC7280058/ /pubmed/32581587 http://dx.doi.org/10.2147/CMAR.S249393 Text en © 2020 Sato et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Sato, Yasuyoshi Fukuda, Naoki Wang, Xiaofei Urasaki, Tetsuya Ohmoto, Akihiro Nakano, Kenji Yunokawa, Mayu Ono, Makiko Sato, Yukiko Mitani, Hiroki Tomomatsu, Junichi Takahashi, Shunji Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title | Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title_full | Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title_fullStr | Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title_full_unstemmed | Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title_short | Efficacy of Nivolumab for Head and Neck Cancer Patients with Primary Sites and Histological Subtypes Excluded from the CheckMate-141 Trial |
title_sort | efficacy of nivolumab for head and neck cancer patients with primary sites and histological subtypes excluded from the checkmate-141 trial |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280058/ https://www.ncbi.nlm.nih.gov/pubmed/32581587 http://dx.doi.org/10.2147/CMAR.S249393 |
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