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重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用

BACKGROUND AND OBJECTIVE: Squamous cell carcinoma (SCC) is a common pathological type of nonsmall cell lung cancer, and advanced lung SCC is incurable. Chemotherapy combined with anti-angiogenesis agents can prolong the patients' survival time. Te aim of the study was to analyze the efcacy and...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973421/
https://www.ncbi.nlm.nih.gov/pubmed/27760596
http://dx.doi.org/10.3779/j.issn.1009-3419.2016.10.06
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description BACKGROUND AND OBJECTIVE: Squamous cell carcinoma (SCC) is a common pathological type of nonsmall cell lung cancer, and advanced lung SCC is incurable. Chemotherapy combined with anti-angiogenesis agents can prolong the patients' survival time. Te aim of the study was to analyze the efcacy and safety of recombinant human endostatin (Endostar) in treating advanced lung SCC. METHODS: We retrospectively analyzed the short-term efficacy and toxicity of recombinant human endostatin combined with traditional chemotherapy regimens in treating 15 advanced lung squamous cell carcinoma patients in Department of Medical Oncology retrospectively, Cancer Hospital, Chinese Academy of Medical Sciences from November 2011 to May 2015. Treatment-related survival was also analyzed. RESULTS: Among the evaluble 14 patients, the best overall response was partial response in 5 patients (35.7%), stable disease in 7 patients (50.0%), and progressive disease in 2 patients (14.3%). Te objective response rate (ORR) was 35.7%, and disease control rate (DCR) was 85.7%. Te median progression-free survival (PFS) was 9.3 months. Te main grade 3 toxicity was neutropenia (2/15, 13.3%) and vomiting (1/15, 6.7%). CONCLUSION: Chemotherapy combined with recombinant human endostatin enabled good objective response in advanced SCC patients and had well security.
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spelling pubmed-59734212018-07-06 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用 Zhongguo Fei Ai Za Zhi 肺鳞癌专题 BACKGROUND AND OBJECTIVE: Squamous cell carcinoma (SCC) is a common pathological type of nonsmall cell lung cancer, and advanced lung SCC is incurable. Chemotherapy combined with anti-angiogenesis agents can prolong the patients' survival time. Te aim of the study was to analyze the efcacy and safety of recombinant human endostatin (Endostar) in treating advanced lung SCC. METHODS: We retrospectively analyzed the short-term efficacy and toxicity of recombinant human endostatin combined with traditional chemotherapy regimens in treating 15 advanced lung squamous cell carcinoma patients in Department of Medical Oncology retrospectively, Cancer Hospital, Chinese Academy of Medical Sciences from November 2011 to May 2015. Treatment-related survival was also analyzed. RESULTS: Among the evaluble 14 patients, the best overall response was partial response in 5 patients (35.7%), stable disease in 7 patients (50.0%), and progressive disease in 2 patients (14.3%). Te objective response rate (ORR) was 35.7%, and disease control rate (DCR) was 85.7%. Te median progression-free survival (PFS) was 9.3 months. Te main grade 3 toxicity was neutropenia (2/15, 13.3%) and vomiting (1/15, 6.7%). CONCLUSION: Chemotherapy combined with recombinant human endostatin enabled good objective response in advanced SCC patients and had well security. 中国肺癌杂志编辑部 2016-10-20 /pmc/articles/PMC5973421/ /pubmed/27760596 http://dx.doi.org/10.3779/j.issn.1009-3419.2016.10.06 Text en 版权所有©《中国肺癌杂志》编辑部2016 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 肺鳞癌专题
重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title_full 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title_fullStr 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title_full_unstemmed 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title_short 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
title_sort 重组人血管内皮抑制素在晚期肺鳞癌治疗中的临床应用
topic 肺鳞癌专题
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973421/
https://www.ncbi.nlm.nih.gov/pubmed/27760596
http://dx.doi.org/10.3779/j.issn.1009-3419.2016.10.06
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