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Salvage treatment with anlotinib for advanced non‐small cell lung cancer

BACKGROUND: This real‐world study assessed the efficacy and toxicity of anlotinib as salvage treatment in Chinese patients with advanced non‐small cell lung cancer (NSCLC). METHODS: The medical records of 81 patients with advanced NSCLC who had failed at least two lines of chemotherapy were retrospe...

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Autores principales: Wu, Di, Nie, Jun, Dai, Ling, Hu, Weiheng, Zhang, Jie, Chen, Xiaoling, Ma, Xiangjuan, Tian, Guangming, Han, Jindi, Han, Sen, Long, Jieran, Wang, Yang, Zhang, Ziran, Fang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610258/
https://www.ncbi.nlm.nih.gov/pubmed/31183998
http://dx.doi.org/10.1111/1759-7714.13120
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author Wu, Di
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Ma, Xiangjuan
Tian, Guangming
Han, Jindi
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
author_facet Wu, Di
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Ma, Xiangjuan
Tian, Guangming
Han, Jindi
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
author_sort Wu, Di
collection PubMed
description BACKGROUND: This real‐world study assessed the efficacy and toxicity of anlotinib as salvage treatment in Chinese patients with advanced non‐small cell lung cancer (NSCLC). METHODS: The medical records of 81 patients with advanced NSCLC who had failed at least two lines of chemotherapy were retrospectively collected. All patients were administered anlotinib treatment until disease progression or intolerance as a result of adverse events. Survival curves were created using the Kaplan–Meier method. The log‐rank test was used for univariate analysis of progression‐free survival (PFS) between groups. Cox regression was used to estimate the statistically significant factors based on univariate analysis. RESULTS: The median PFS was five months (95% confidence interval [CI] 3.5–6.5). The objective response rate (ORR) was 7% and the disease control rate (DCR) was 84%. The following subgroups of patients had longer PFS (P < 0.05): squamous cell carcinoma, no brain or liver metastases, Eastern Cooperative Oncology Group performance status (ECOG PS) of 0–1, and no previous VEGF‐tyrosine kinase inhibitor treatment. The results of Cox regression indicated that an ECOG PS of 0–1 (hazard ratio 0.152, 95% CI 0.057–0.403; P = 0.00) and patients without brain metastases (hazard ratio 0.421, 95% CI 0.195–0.911; P = 0.028) had longer PFS following anlotinib treatment. CONCLUSION: Anlotinib, which is well tolerated, plays a significant role in the salvage treatment of advanced NSCLC. Patients with advanced NSCLC with an ECOG PS of 0–1 and no brain metastases achieved longer PFS following anlotinib salvage treatment.
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spelling pubmed-66102582019-07-16 Salvage treatment with anlotinib for advanced non‐small cell lung cancer Wu, Di Nie, Jun Dai, Ling Hu, Weiheng Zhang, Jie Chen, Xiaoling Ma, Xiangjuan Tian, Guangming Han, Jindi Han, Sen Long, Jieran Wang, Yang Zhang, Ziran Fang, Jian Thorac Cancer Original Articles BACKGROUND: This real‐world study assessed the efficacy and toxicity of anlotinib as salvage treatment in Chinese patients with advanced non‐small cell lung cancer (NSCLC). METHODS: The medical records of 81 patients with advanced NSCLC who had failed at least two lines of chemotherapy were retrospectively collected. All patients were administered anlotinib treatment until disease progression or intolerance as a result of adverse events. Survival curves were created using the Kaplan–Meier method. The log‐rank test was used for univariate analysis of progression‐free survival (PFS) between groups. Cox regression was used to estimate the statistically significant factors based on univariate analysis. RESULTS: The median PFS was five months (95% confidence interval [CI] 3.5–6.5). The objective response rate (ORR) was 7% and the disease control rate (DCR) was 84%. The following subgroups of patients had longer PFS (P < 0.05): squamous cell carcinoma, no brain or liver metastases, Eastern Cooperative Oncology Group performance status (ECOG PS) of 0–1, and no previous VEGF‐tyrosine kinase inhibitor treatment. The results of Cox regression indicated that an ECOG PS of 0–1 (hazard ratio 0.152, 95% CI 0.057–0.403; P = 0.00) and patients without brain metastases (hazard ratio 0.421, 95% CI 0.195–0.911; P = 0.028) had longer PFS following anlotinib treatment. CONCLUSION: Anlotinib, which is well tolerated, plays a significant role in the salvage treatment of advanced NSCLC. Patients with advanced NSCLC with an ECOG PS of 0–1 and no brain metastases achieved longer PFS following anlotinib salvage treatment. John Wiley & Sons Australia, Ltd 2019-06-10 2019-07 /pmc/articles/PMC6610258/ /pubmed/31183998 http://dx.doi.org/10.1111/1759-7714.13120 Text en © 2019 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
Wu, Di
Nie, Jun
Dai, Ling
Hu, Weiheng
Zhang, Jie
Chen, Xiaoling
Ma, Xiangjuan
Tian, Guangming
Han, Jindi
Han, Sen
Long, Jieran
Wang, Yang
Zhang, Ziran
Fang, Jian
Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title_full Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title_fullStr Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title_full_unstemmed Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title_short Salvage treatment with anlotinib for advanced non‐small cell lung cancer
title_sort salvage treatment with anlotinib for advanced non‐small cell lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610258/
https://www.ncbi.nlm.nih.gov/pubmed/31183998
http://dx.doi.org/10.1111/1759-7714.13120
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