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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...

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Autores principales: Sato, Yasuyoshi, Fukuda, Naoki, Wang, Xiaofei, Urasaki, Tetsuya, Ohmoto, Akihiro, Nakano, Kenji, Yunokawa, Mayu, Ono, Makiko, Sato, Yukiko, Mitani, Hiroki, Tomomatsu, Junichi, Takahashi, Shunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
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.
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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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