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克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性

BACKGROUND AND OBJECTIVE: Anaplastic lymphoma kinase (ALK) positive in non-small cell lung cancer (NSCLC) was about 5%-7% and ALK tyrosine kinase inhibitor (TKI) was the standard treatment in NSCLC. The aim of this study is to evaluate the efficacy and safety of crizotinib in patients with advanced...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717874/
https://www.ncbi.nlm.nih.gov/pubmed/31451138
http://dx.doi.org/10.3779/j.issn.1009-3419.2019.08.02
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description BACKGROUND AND OBJECTIVE: Anaplastic lymphoma kinase (ALK) positive in non-small cell lung cancer (NSCLC) was about 5%-7% and ALK tyrosine kinase inhibitor (TKI) was the standard treatment in NSCLC. The aim of this study is to evaluate the efficacy and safety of crizotinib in patients with advanced ALK gene-positive or recurrent NSCLC. METHODS: Three methods were used to screen patients with advanced or recurrent NSCLC harboring ALK gene fusion/translocation. The patients with ALK positive tested by flourescence in situ hybridization (FISH) was given orally crizotinib, 250 mg, bid. The objective response rate (ORR), progression-free survival (PFS) and safety were evaluated. RESULTS: A total of 226 patients were screened, 39 of whom had ALK fusion or translocation, and 37 were enrolled in the study. 35 patients were evaluated for objective response, ORR was 70.3%, and disease control rate (DCR) was 94.6%, and median PFS was 11.8 mon. The main adverse reactions were elevated transaminase (Grade 1, 91.7%), elevated transaminases (Grade 2, 23.4%), nausea (Grade 1, 75.6%), anemia (Grade 1-2, 62.3%), visual impairment (Grade 1, 21.8%), weight loss (Grade 1, 31.4%), pneumonia (Grade 2, 3.5%). CONCLUSION: Crizotinib can be used for the treatment of advanced NSCLC with ALK fusion/translocation. It is highly effective and well tolerated.
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spelling pubmed-67178742019-09-02 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Anaplastic lymphoma kinase (ALK) positive in non-small cell lung cancer (NSCLC) was about 5%-7% and ALK tyrosine kinase inhibitor (TKI) was the standard treatment in NSCLC. The aim of this study is to evaluate the efficacy and safety of crizotinib in patients with advanced ALK gene-positive or recurrent NSCLC. METHODS: Three methods were used to screen patients with advanced or recurrent NSCLC harboring ALK gene fusion/translocation. The patients with ALK positive tested by flourescence in situ hybridization (FISH) was given orally crizotinib, 250 mg, bid. The objective response rate (ORR), progression-free survival (PFS) and safety were evaluated. RESULTS: A total of 226 patients were screened, 39 of whom had ALK fusion or translocation, and 37 were enrolled in the study. 35 patients were evaluated for objective response, ORR was 70.3%, and disease control rate (DCR) was 94.6%, and median PFS was 11.8 mon. The main adverse reactions were elevated transaminase (Grade 1, 91.7%), elevated transaminases (Grade 2, 23.4%), nausea (Grade 1, 75.6%), anemia (Grade 1-2, 62.3%), visual impairment (Grade 1, 21.8%), weight loss (Grade 1, 31.4%), pneumonia (Grade 2, 3.5%). CONCLUSION: Crizotinib can be used for the treatment of advanced NSCLC with ALK fusion/translocation. It is highly effective and well tolerated. 中国肺癌杂志编辑部 2019-08-20 /pmc/articles/PMC6717874/ /pubmed/31451138 http://dx.doi.org/10.3779/j.issn.1009-3419.2019.08.02 Text en 版权所有©《中国肺癌杂志》编辑部2019 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
克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title_full 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title_fullStr 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title_full_unstemmed 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title_short 克唑替尼治疗晚期或复发性ALK阳性非小细胞肺癌的疗效和安全性
title_sort 克唑替尼治疗晚期或复发性alk阳性非小细胞肺癌的疗效和安全性
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717874/
https://www.ncbi.nlm.nih.gov/pubmed/31451138
http://dx.doi.org/10.3779/j.issn.1009-3419.2019.08.02
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