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紫杉醇-卡铂联合贝伐珠单抗作为晚期非鳞状非小细胞肺癌二线治疗的疗效:铂类药物再挑战。

Efficacy of paclitaxel-carboplatin with bevacizumab as a late-line therapy for patients with advanced nonsquamous non-small cell lung cancer: A platinum rechallenge.

机构信息

Department of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan.

出版信息

Thorac Cancer. 2023 Nov;14(31):3140-3146. doi: 10.1111/1759-7714.15107. Epub 2023 Sep 12.

DOI:10.1111/1759-7714.15107
PMID:37699787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10626222/
Abstract

BACKGROUND

There is no well-established late-line treatment for advanced nonsquamous non-small cell lung cancer (NSCLC). Therefore, we retrospectively determined the efficacy and safety of platinum rechallenge with paclitaxel-carboplatin and bevacizumab in patients with nonsquamous NSCLC as a late-line therapy in a clinical setting.

METHODS

Thirty patients with nonsquamous NSCLC who received paclitaxel-carboplatin with bevacizumab therapy as a late-line treatment at Sendai Kousei Hospital (Miyagi, Japan) between December 2011 and December 2021 were enrolled into the study. The efficacy and safety of this treatment were evaluated. The patients were further categorized into responders and nonresponders, and predictive factors of treatment response were estimated.

RESULTS

The median progression-free survival (PFS) was 6.3 (range, 4.9-6.8) months, and the median overall survival (OS) was 11.8 (range, 7.2-17.2) months. There were no significant differences in PFS and OS between patients with and those without epidermal growth factor receptor mutations. In the univariate analyses of this study, responders were younger than nonresponders (p = 0.012). No fatal adverse events were reported.

CONCLUSIONS

With the increase in the number of treatment options in recent years, the sequence of treatments and overall therapeutic strategy are becoming increasingly important. Thus, platinum rechallenge with paclitaxel-carboplatin and bevacizumab, a late-line treatment for patients with nonsquamous NSCLC, may be an effective therapeutic option.

摘要

背景

晚期非鳞状非小细胞肺癌(NSCLC)缺乏成熟的后线治疗方案。因此,我们回顾性评估了在临床实践中,紫杉醇-卡铂联合贝伐珠单抗作为晚期治疗方案,用于治疗非鳞状 NSCLC 患者的疗效和安全性。

方法

2011 年 12 月至 2021 年 12 月,日本仙台市仙台光成医院对 30 例接受紫杉醇-卡铂联合贝伐珠单抗治疗的非鳞状 NSCLC 患者进行了回顾性分析,评估了该治疗方案的疗效和安全性。根据患者的治疗反应将其分为应答者和无应答者,并估计了治疗反应的预测因素。

结果

中位无进展生存期(PFS)为 6.3 个月(范围,4.9-6.8 个月),中位总生存期(OS)为 11.8 个月(范围,7.2-17.2 个月)。EGFR 基因突变患者与无 EGFR 基因突变患者的 PFS 和 OS 无显著差异。单因素分析显示,应答者较无应答者年轻(p=0.012)。未发生致命不良事件。

结论

近年来,随着治疗方案数量的增加,治疗顺序和整体治疗策略变得越来越重要。因此,紫杉醇-卡铂联合贝伐珠单抗作为晚期治疗方案,对非鳞状 NSCLC 患者进行铂类药物再挑战可能是一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a86/10626222/f199e339fb3e/TCA-14-3140-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a86/10626222/f43ece361f60/TCA-14-3140-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a86/10626222/f199e339fb3e/TCA-14-3140-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a86/10626222/f43ece361f60/TCA-14-3140-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a86/10626222/f199e339fb3e/TCA-14-3140-g003.jpg

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