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替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析

BACKGROUND AND OBJECTIVE: There is no standard treatment for advanced non-small cell lung cancer (NSCLC) after the failure of two lines of chemotherapy, S-1 as the third generation of fluorouracil derivate with well safety and low toxicity, presented some efficacy in lung cancer treatment. The aim o...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022025/
https://www.ncbi.nlm.nih.gov/pubmed/29945701
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.06.03
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description BACKGROUND AND OBJECTIVE: There is no standard treatment for advanced non-small cell lung cancer (NSCLC) after the failure of two lines of chemotherapy, S-1 as the third generation of fluorouracil derivate with well safety and low toxicity, presented some efficacy in lung cancer treatment. The aim of this study is to explore the efficacy of S-1 for advanced NSCLC patients treated with two or more prior chemotherapy regimens. METHODS: We performed a retrospective analysis of 105 NSCLC patients treated with S-1 monotherapy or S-1 contained chemotherapy as the third or more line of treatment in our hospital from January 2014 to April 2017. S-1 was administrated orally twice daily for 2 weeks, followed by one week of rest, the dose of drug was determined by body surface area (< 1.25 m(2), 80 mg/d; 1.25 m(2)-1.5 m(2), 100 mg/d; ≥1.5 m(2), 120 mg/d), platinum or the third-generation chemotherapy drugs could be combinedly used. Clinical response was assigned every cycle according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, Kaplan-Meier analysis was used to estimate progression-free survival (PFS). RESULTS: 42 patients received S-1 monotherapy, the other 63 patients received combined regimens, the median treatment line was 4 (3-11) and the median treatment cycle was 2 (1-14). No complete response (CR) were observed, there were 4 patients with partial response (PR), 34 patients with stable disease (SD) and 67 patients with progressive disease (PD), the objective response rate (ORR) was 3.81%, disease control rate (DCR) was 36.19%. The median PFS was 1.90 months (0.67 months-10.83 months), no difference between monotherapy and combined group (DCR: 28.56% vs 41.27%, P=0.185), the liver metastasis showed poorer PFS (1.40 months vs 1.93 months, P=0.042). CONCLUSION: S-1 presented some activity in advanced NSCLC treated with more than two lines of treatment. The addition of other drugs cannot improve efficacy. S-1 monotherapy can be used as a choice for heavily-treated patients.
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spelling pubmed-60220252018-07-06 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: There is no standard treatment for advanced non-small cell lung cancer (NSCLC) after the failure of two lines of chemotherapy, S-1 as the third generation of fluorouracil derivate with well safety and low toxicity, presented some efficacy in lung cancer treatment. The aim of this study is to explore the efficacy of S-1 for advanced NSCLC patients treated with two or more prior chemotherapy regimens. METHODS: We performed a retrospective analysis of 105 NSCLC patients treated with S-1 monotherapy or S-1 contained chemotherapy as the third or more line of treatment in our hospital from January 2014 to April 2017. S-1 was administrated orally twice daily for 2 weeks, followed by one week of rest, the dose of drug was determined by body surface area (< 1.25 m(2), 80 mg/d; 1.25 m(2)-1.5 m(2), 100 mg/d; ≥1.5 m(2), 120 mg/d), platinum or the third-generation chemotherapy drugs could be combinedly used. Clinical response was assigned every cycle according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, Kaplan-Meier analysis was used to estimate progression-free survival (PFS). RESULTS: 42 patients received S-1 monotherapy, the other 63 patients received combined regimens, the median treatment line was 4 (3-11) and the median treatment cycle was 2 (1-14). No complete response (CR) were observed, there were 4 patients with partial response (PR), 34 patients with stable disease (SD) and 67 patients with progressive disease (PD), the objective response rate (ORR) was 3.81%, disease control rate (DCR) was 36.19%. The median PFS was 1.90 months (0.67 months-10.83 months), no difference between monotherapy and combined group (DCR: 28.56% vs 41.27%, P=0.185), the liver metastasis showed poorer PFS (1.40 months vs 1.93 months, P=0.042). CONCLUSION: S-1 presented some activity in advanced NSCLC treated with more than two lines of treatment. The addition of other drugs cannot improve efficacy. S-1 monotherapy can be used as a choice for heavily-treated patients. 中国肺癌杂志编辑部 2018-06-20 /pmc/articles/PMC6022025/ /pubmed/29945701 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.06.03 Text en 版权所有©《中国肺癌杂志》编辑部2018 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
替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title_full 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title_fullStr 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title_full_unstemmed 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title_short 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
title_sort 替吉奥治疗晚期非小细胞肺癌三线及以上患者的疗效分析
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022025/
https://www.ncbi.nlm.nih.gov/pubmed/29945701
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.06.03
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