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克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察

BACKGROUND AND OBJECTIVE: The aim of this study is to explore clinical efficacy of crizotinib in advanced anaplastic lymphoma kinase (ALK) positive non-small cell lung cancer. METHODS: Twenty-eight patients with advanced non-small cell lung cancer habouring ALK positive were randomly divided into cr...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000091/
https://www.ncbi.nlm.nih.gov/pubmed/26483333
http://dx.doi.org/10.3779/j.issn.1009-3419.2015.10.03
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description BACKGROUND AND OBJECTIVE: The aim of this study is to explore clinical efficacy of crizotinib in advanced anaplastic lymphoma kinase (ALK) positive non-small cell lung cancer. METHODS: Twenty-eight patients with advanced non-small cell lung cancer habouring ALK positive were randomly divided into crizotinib group (n=14) and chemotherapy group (n=14).Patients in the crizotinib group were receive oral treatment with crizotinib (250 mg) twice daily.Patients in the chemotherapy group were administrated docetaxel injection (75 mg/m(2)) every three weeks and every patient was treated at least 3 period.Then clinical efficacy was observed after 12 mo followed-up. RESULTS: Effective rate of patients in the crizotinib group was 64.29%.It was significantly higher than that of the chemotherapy group (21.43%)(P=0.026).The stable rate of patients in the crizotinib group was 85.71%.It was significantly higher than that of the chemotherapy group 40.86% (χ(2)=5.600, P=0.018).Median progression free survival (PFS) of the crizotinib group was 7.0 mo.It was longer than that of the chemotherapy group (4.0 mo)(P=0.002). CONCLUSION: Crizotinib is superior to standard chemotherapy in patients with previously treated, advanced ALK positive non-small cell lung cancer.The median PFS of patients is shorter.It can improve the quality of life about patients.
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spelling pubmed-60000912018-07-06 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: The aim of this study is to explore clinical efficacy of crizotinib in advanced anaplastic lymphoma kinase (ALK) positive non-small cell lung cancer. METHODS: Twenty-eight patients with advanced non-small cell lung cancer habouring ALK positive were randomly divided into crizotinib group (n=14) and chemotherapy group (n=14).Patients in the crizotinib group were receive oral treatment with crizotinib (250 mg) twice daily.Patients in the chemotherapy group were administrated docetaxel injection (75 mg/m(2)) every three weeks and every patient was treated at least 3 period.Then clinical efficacy was observed after 12 mo followed-up. RESULTS: Effective rate of patients in the crizotinib group was 64.29%.It was significantly higher than that of the chemotherapy group (21.43%)(P=0.026).The stable rate of patients in the crizotinib group was 85.71%.It was significantly higher than that of the chemotherapy group 40.86% (χ(2)=5.600, P=0.018).Median progression free survival (PFS) of the crizotinib group was 7.0 mo.It was longer than that of the chemotherapy group (4.0 mo)(P=0.002). CONCLUSION: Crizotinib is superior to standard chemotherapy in patients with previously treated, advanced ALK positive non-small cell lung cancer.The median PFS of patients is shorter.It can improve the quality of life about patients. 中国肺癌杂志编辑部 2015-10-20 /pmc/articles/PMC6000091/ /pubmed/26483333 http://dx.doi.org/10.3779/j.issn.1009-3419.2015.10.03 Text en 版权所有©《中国肺癌杂志》编辑部2015 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 临床研究
克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title_full 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title_fullStr 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title_full_unstemmed 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title_short 克唑替尼治疗ALK阳性晚期非小细胞肺癌患者的疗效观察
title_sort 克唑替尼治疗alk阳性晚期非小细胞肺癌患者的疗效观察
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000091/
https://www.ncbi.nlm.nih.gov/pubmed/26483333
http://dx.doi.org/10.3779/j.issn.1009-3419.2015.10.03
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