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Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population

Head and neck squamous cell carcinoma (HNSCC) has a high prevalence and is a major cause of cancer deaths in Taiwan. However, there is still no effective salvage therapy that prolongs the life expectancy of patients with recurrent/metastatic (R/M) HNSCC. Immune checkpoint therapy that targets the pr...

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Autores principales: Chen, Wen-Chun, Chu, Pen-Yuan, Lee, Yu-Ting, Lu, Wen-Bin, Liu, Chun-Yu, Chang, Peter Mu-Hsin, Yang, Muh-Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392576/
https://www.ncbi.nlm.nih.gov/pubmed/29384959
http://dx.doi.org/10.1097/MD.0000000000009519
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author Chen, Wen-Chun
Chu, Pen-Yuan
Lee, Yu-Ting
Lu, Wen-Bin
Liu, Chun-Yu
Chang, Peter Mu-Hsin
Yang, Muh-Hwa
author_facet Chen, Wen-Chun
Chu, Pen-Yuan
Lee, Yu-Ting
Lu, Wen-Bin
Liu, Chun-Yu
Chang, Peter Mu-Hsin
Yang, Muh-Hwa
author_sort Chen, Wen-Chun
collection PubMed
description Head and neck squamous cell carcinoma (HNSCC) has a high prevalence and is a major cause of cancer deaths in Taiwan. However, there is still no effective salvage therapy that prolongs the life expectancy of patients with recurrent/metastatic (R/M) HNSCC. Immune checkpoint therapy that targets the programmed cell death protein 1 (PD-1) may provide clinical benefit for these patients. We analyzed 22 R/M HNSCC patients who received pembrolizumab, a monoclonal antibody against PD-1, as salvage therapy. Intravenous pembrolizumab was given at a fixed dosage of 100 or 200 mg every 3 weeks. Three patients also received local palliative radiotherapy, but no patients received chemotherapy or targeted drugs. Seventeen patients (77.3%) received at least 3 cycles of pembrolizumab. Based on Response Evaluation Criteria in Solid Tumors criteria (ver. 1.1), 2 patients (9.1%) had complete response, 5 (22.7%) had partial response, and 6 (27.3%) had stable disease, corresponding to a disease control rate of 59.1%. Four patients had confirmed disease progression, 2 of whom had continuous progression over the target lesion after shrinkage of other metastases. One patient developed immune-related pneumonitis that resolved quickly after steroid treatment. Another patient developed itchy skin rashes immediately after administration of pembrolizumab, and this was controlled by an antihistamine. There were no other severe adverse effects. Pembrolizumab is beneficial and well-tolerated for some patients with refractory R/M HNSCC. However, it is important to identify biomarkers to identify the most responsive patients when designing future trials.
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spelling pubmed-63925762019-03-15 Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population Chen, Wen-Chun Chu, Pen-Yuan Lee, Yu-Ting Lu, Wen-Bin Liu, Chun-Yu Chang, Peter Mu-Hsin Yang, Muh-Hwa Medicine (Baltimore) Research Article Head and neck squamous cell carcinoma (HNSCC) has a high prevalence and is a major cause of cancer deaths in Taiwan. However, there is still no effective salvage therapy that prolongs the life expectancy of patients with recurrent/metastatic (R/M) HNSCC. Immune checkpoint therapy that targets the programmed cell death protein 1 (PD-1) may provide clinical benefit for these patients. We analyzed 22 R/M HNSCC patients who received pembrolizumab, a monoclonal antibody against PD-1, as salvage therapy. Intravenous pembrolizumab was given at a fixed dosage of 100 or 200 mg every 3 weeks. Three patients also received local palliative radiotherapy, but no patients received chemotherapy or targeted drugs. Seventeen patients (77.3%) received at least 3 cycles of pembrolizumab. Based on Response Evaluation Criteria in Solid Tumors criteria (ver. 1.1), 2 patients (9.1%) had complete response, 5 (22.7%) had partial response, and 6 (27.3%) had stable disease, corresponding to a disease control rate of 59.1%. Four patients had confirmed disease progression, 2 of whom had continuous progression over the target lesion after shrinkage of other metastases. One patient developed immune-related pneumonitis that resolved quickly after steroid treatment. Another patient developed itchy skin rashes immediately after administration of pembrolizumab, and this was controlled by an antihistamine. There were no other severe adverse effects. Pembrolizumab is beneficial and well-tolerated for some patients with refractory R/M HNSCC. However, it is important to identify biomarkers to identify the most responsive patients when designing future trials. Wolters Kluwer Health 2017-12-29 /pmc/articles/PMC6392576/ /pubmed/29384959 http://dx.doi.org/10.1097/MD.0000000000009519 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Chen, Wen-Chun
Chu, Pen-Yuan
Lee, Yu-Ting
Lu, Wen-Bin
Liu, Chun-Yu
Chang, Peter Mu-Hsin
Yang, Muh-Hwa
Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title_full Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title_fullStr Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title_full_unstemmed Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title_short Pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an Asian population
title_sort pembrolizumab for recurrent/metastatic head and neck squamous cell carcinoma in an asian population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392576/
https://www.ncbi.nlm.nih.gov/pubmed/29384959
http://dx.doi.org/10.1097/MD.0000000000009519
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