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Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma
BACKGROUND: This study was conducted to evaluate the efficacy and safety of nimotuzumab combined with chemotherapy as first‐line therapy in advanced lung squamous cell carcinoma (LSCC), and to explore predictive biomarkers of the efficacy of nimotuzumab. METHODS: A retrospective study was conducted...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068447/ https://www.ncbi.nlm.nih.gov/pubmed/29920955 http://dx.doi.org/10.1111/1759-7714.12789 |
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author | Si, Xiaoyan Wu, Shafei Wang, Hanping Zhang, Xiaotong Wang, Mengzhao Zeng, Xuan Zhang, Li |
author_facet | Si, Xiaoyan Wu, Shafei Wang, Hanping Zhang, Xiaotong Wang, Mengzhao Zeng, Xuan Zhang, Li |
author_sort | Si, Xiaoyan |
collection | PubMed |
description | BACKGROUND: This study was conducted to evaluate the efficacy and safety of nimotuzumab combined with chemotherapy as first‐line therapy in advanced lung squamous cell carcinoma (LSCC), and to explore predictive biomarkers of the efficacy of nimotuzumab. METHODS: A retrospective study was conducted of patients with advanced LSCC administered nimotuzumab combined with chemotherapy as first‐line therapy from June 2012 to December 2016 at the Department of Respiratory Medicine, Peking Union Medical College Hospital. The associations between EGFR expression, EGFR gene copy numbers, and clinical efficacy were detected by immunohistochemistry and fluorescence in situ hybridization (FISH). RESULTS: Twenty‐six patients were enrolled, including 22 men and 4 women. The objective response rate was 50% and the disease control rate was 100%. The median progression‐free survival (PFS) and overall survival were 6.7 and 16.3 months, respectively. Patients whose samples were tested via FISH and showed positive EGFR expression had a trend of longer median PFS (10.0 months; P = 0.10). Adverse effects included 15 cases (57.7%) of bone marrow suppression, 15 (57.7%) of sensory neuropathy, 14 (53.8%) of alopecia, nine (34.6%) of nausea/vomiting and one case (3.8%) of elevated creatinine level. All adverse effects were attributed to chemotherapy. CONCLUSION: Nimotuzumab combined with chemotherapy might be a possible option as first‐line therapy in patients with advanced LSCC. EGFR gene copy number examined by FISH might be a possible predictive biomarker. |
format | Online Article Text |
id | pubmed-6068447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60684472018-08-03 Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma Si, Xiaoyan Wu, Shafei Wang, Hanping Zhang, Xiaotong Wang, Mengzhao Zeng, Xuan Zhang, Li Thorac Cancer Original Articles BACKGROUND: This study was conducted to evaluate the efficacy and safety of nimotuzumab combined with chemotherapy as first‐line therapy in advanced lung squamous cell carcinoma (LSCC), and to explore predictive biomarkers of the efficacy of nimotuzumab. METHODS: A retrospective study was conducted of patients with advanced LSCC administered nimotuzumab combined with chemotherapy as first‐line therapy from June 2012 to December 2016 at the Department of Respiratory Medicine, Peking Union Medical College Hospital. The associations between EGFR expression, EGFR gene copy numbers, and clinical efficacy were detected by immunohistochemistry and fluorescence in situ hybridization (FISH). RESULTS: Twenty‐six patients were enrolled, including 22 men and 4 women. The objective response rate was 50% and the disease control rate was 100%. The median progression‐free survival (PFS) and overall survival were 6.7 and 16.3 months, respectively. Patients whose samples were tested via FISH and showed positive EGFR expression had a trend of longer median PFS (10.0 months; P = 0.10). Adverse effects included 15 cases (57.7%) of bone marrow suppression, 15 (57.7%) of sensory neuropathy, 14 (53.8%) of alopecia, nine (34.6%) of nausea/vomiting and one case (3.8%) of elevated creatinine level. All adverse effects were attributed to chemotherapy. CONCLUSION: Nimotuzumab combined with chemotherapy might be a possible option as first‐line therapy in patients with advanced LSCC. EGFR gene copy number examined by FISH might be a possible predictive biomarker. John Wiley & Sons Australia, Ltd 2018-06-19 2018-08 /pmc/articles/PMC6068447/ /pubmed/29920955 http://dx.doi.org/10.1111/1759-7714.12789 Text en © 2018 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Si, Xiaoyan Wu, Shafei Wang, Hanping Zhang, Xiaotong Wang, Mengzhao Zeng, Xuan Zhang, Li Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title | Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title_full | Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title_fullStr | Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title_full_unstemmed | Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title_short | Nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
title_sort | nimotuzumab combined with chemotherapy as first‐line treatment for advanced lung squamous cell carcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068447/ https://www.ncbi.nlm.nih.gov/pubmed/29920955 http://dx.doi.org/10.1111/1759-7714.12789 |
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