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Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors
Penile squamous cell carcinoma (SCC) is a rare malignancy with limited treatment options when the tumor is unresectable and/or chemorefractory. Triplet systemic chemotherapy regimens including taxane and cisplatin are recommended, but the response duration can be short and the treatment-related toxi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673798/ https://www.ncbi.nlm.nih.gov/pubmed/29184782 http://dx.doi.org/10.21037/tau.2017.03.92 |
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author | Gu, Weijie Zhu, Yao Ye, Dingwei |
author_facet | Gu, Weijie Zhu, Yao Ye, Dingwei |
author_sort | Gu, Weijie |
collection | PubMed |
description | Penile squamous cell carcinoma (SCC) is a rare malignancy with limited treatment options when the tumor is unresectable and/or chemorefractory. Triplet systemic chemotherapy regimens including taxane and cisplatin are recommended, but the response duration can be short and the treatment-related toxicity high. Only a small proportion of patients survive 1 year or longer with the current standard treatment paradigm. Beyond chemotherapy, the use of novel targeted agents, either alone or in combination with traditional chemotherapeutic agents, has appeared to have promising efficacy in patients with platinum-refractory penile cancer. The frequent overexpression of PD-L1 in advanced penile SCC indicates the potential efficacy of PD-1 inhibitors. Upcoming clinical trials using the immune check-point inhibitors may provide exciting landscape and change the paradigm for patients in the future. |
format | Online Article Text |
id | pubmed-5673798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-56737982017-11-28 Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors Gu, Weijie Zhu, Yao Ye, Dingwei Transl Androl Urol Review Article Penile squamous cell carcinoma (SCC) is a rare malignancy with limited treatment options when the tumor is unresectable and/or chemorefractory. Triplet systemic chemotherapy regimens including taxane and cisplatin are recommended, but the response duration can be short and the treatment-related toxicity high. Only a small proportion of patients survive 1 year or longer with the current standard treatment paradigm. Beyond chemotherapy, the use of novel targeted agents, either alone or in combination with traditional chemotherapeutic agents, has appeared to have promising efficacy in patients with platinum-refractory penile cancer. The frequent overexpression of PD-L1 in advanced penile SCC indicates the potential efficacy of PD-1 inhibitors. Upcoming clinical trials using the immune check-point inhibitors may provide exciting landscape and change the paradigm for patients in the future. AME Publishing Company 2017-10 /pmc/articles/PMC5673798/ /pubmed/29184782 http://dx.doi.org/10.21037/tau.2017.03.92 Text en 2017 Translational Andrology and Urology. All rights reserved. |
spellingShingle | Review Article Gu, Weijie Zhu, Yao Ye, Dingwei Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title | Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title_full | Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title_fullStr | Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title_full_unstemmed | Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title_short | Beyond chemotherapy for advanced disease—the role of EGFR and PD-1 inhibitors |
title_sort | beyond chemotherapy for advanced disease—the role of egfr and pd-1 inhibitors |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673798/ https://www.ncbi.nlm.nih.gov/pubmed/29184782 http://dx.doi.org/10.21037/tau.2017.03.92 |
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