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苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析

BACKGROUND AND OBJECTIVE: Advanced non-small cell lung cancer (NSCLC) is a common malignancy that is incurable. No standard treatment exists for recurrent patients. This article analyzed the efficacy and safety of sunitinib (37.5 mg qd) on a continuous daily dosing (CDD) schedule in treating recurre...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015172/
https://www.ncbi.nlm.nih.gov/pubmed/24113004
http://dx.doi.org/10.3779/j.issn.1009-3419.2013.10.04
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description BACKGROUND AND OBJECTIVE: Advanced non-small cell lung cancer (NSCLC) is a common malignancy that is incurable. No standard treatment exists for recurrent patients. This article analyzed the efficacy and safety of sunitinib (37.5 mg qd) on a continuous daily dosing (CDD) schedule in treating recurrent advanced NSCLC. METHODS: We retrospectively analyzed the short-term efficacy and toxicity of sunitinib CDD in treating 17 patients who had previously undergone multiple cycles of therapy for advanced NSCLC in our hospital from January 2011 to December 2012. Treatment-related survival was also analyzed. RESULTS: Among the 17 patients, the best overall response was partial response in 1 patient (5.9%), stable disease in 7 patients (41.2%), and progressive disease in 9 patients (52.9%). The overall response rate was 5.9%, and the disease control rate was 47.1%. The median progression-free survival was 4.4 months (95%CI: 4.05-7.46). The main grade 3/4 toxicity was hand-foot skin reaction. CONCLUSION: Sunitinib (37.5 mg QD) CDD enabled good objective response in advanced NSCLC patients who had previously received multiple cycles of treatment and was well tolerated.
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spelling pubmed-60151722018-07-06 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析 Zhongguo Fei Ai Za Zhi Tki耐药专题 BACKGROUND AND OBJECTIVE: Advanced non-small cell lung cancer (NSCLC) is a common malignancy that is incurable. No standard treatment exists for recurrent patients. This article analyzed the efficacy and safety of sunitinib (37.5 mg qd) on a continuous daily dosing (CDD) schedule in treating recurrent advanced NSCLC. METHODS: We retrospectively analyzed the short-term efficacy and toxicity of sunitinib CDD in treating 17 patients who had previously undergone multiple cycles of therapy for advanced NSCLC in our hospital from January 2011 to December 2012. Treatment-related survival was also analyzed. RESULTS: Among the 17 patients, the best overall response was partial response in 1 patient (5.9%), stable disease in 7 patients (41.2%), and progressive disease in 9 patients (52.9%). The overall response rate was 5.9%, and the disease control rate was 47.1%. The median progression-free survival was 4.4 months (95%CI: 4.05-7.46). The main grade 3/4 toxicity was hand-foot skin reaction. CONCLUSION: Sunitinib (37.5 mg QD) CDD enabled good objective response in advanced NSCLC patients who had previously received multiple cycles of treatment and was well tolerated. 中国肺癌杂志编辑部 2013-10-20 /pmc/articles/PMC6015172/ /pubmed/24113004 http://dx.doi.org/10.3779/j.issn.1009-3419.2013.10.04 Text en 版权所有©《中国肺癌杂志》编辑部2013 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 Tki耐药专题
苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title_full 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title_fullStr 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title_full_unstemmed 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title_short 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
title_sort 苹果酸舒尼替尼治疗多次复发的晚期非小细胞肺癌疗效与安全性分析
topic Tki耐药专题
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015172/
https://www.ncbi.nlm.nih.gov/pubmed/24113004
http://dx.doi.org/10.3779/j.issn.1009-3419.2013.10.04
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