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表皮生长因子受体激活突变的非小细胞肺癌恶性胸腔积液的序贯治疗策略

Sequential treatment strategy for malignant pleural effusion in non-small cell lung cancer with the activated epithelial grow factor receptor mutation.

作者信息

Lin Jian-Bo, Lai Fan-Cai, Li Xu, Tu Yuan-Rong, Lin Min, Qiu Min-Lian, Luo Rong-Gang, Liu Bo, Lin Jing-Wei

机构信息

a Department of Thoracic Surgery , First Affiliated Hospital, Fujian Medical University , Fuzhou City , People's Republic of China.

b Lung Cancer Center, First Affiliated Hospital, Fujian Medical University , Fuzhou City , People's Republic of China.

出版信息

J Drug Target. 2017 Feb;25(2):119-124. doi: 10.1080/1061186X.2016.1200590. Epub 2016 Jun 29.

Abstract

With the advent of molecularly targeted therapy, it is necessary to reconsider the strategy for malignant pleural effusion in non-small-cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations. The aim of this study was to evaluate the efficacy of a two-line sequential treatment strategy in this patient subgroup. First-line treatment was gefitinib (250 mg/day) until disease progression. Second-line treatment was thoracoscopic talc pleurodesis followed by chemotherapy. Primary endpoints were the overall response and progression-free survival rates after first-line treatment, and the overall survival rate after first- and second-line treatment. Secondary endpoints were the success rate of thoracoscopic talc pleurodesis and gefitinib toxicity. Among the 76 patients enrolled, 61 (80%) were female and the median age was 62 years. The overall response rate after first-line treatment was 92.1% and median progression-free survival was 15 months. The success rate for thoracoscopic talc pleurodesis in 33 patients was 94%. Median follow-up was 35 months. Median overall survival was 39 months. The 1- and 3-year overall survival rates were 86.4% and 46.1%, respectively. The two-line sequential treatment strategy enhanced survival. These preliminary findings provide an insight into novel therapeutic models for malignant pleural effusion in NSCLC harbouring EGFR mutations.

摘要

随着分子靶向治疗的出现,有必要重新考虑对具有表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)恶性胸腔积液的治疗策略。本研究的目的是评估该患者亚组中两线序贯治疗策略的疗效。一线治疗为吉非替尼(250毫克/天),直至疾病进展。二线治疗为胸腔镜滑石粉胸膜固定术,随后进行化疗。主要终点是一线治疗后的总缓解率和无进展生存率,以及一线和二线治疗后的总生存率。次要终点是胸腔镜滑石粉胸膜固定术的成功率和吉非替尼的毒性。在纳入的76例患者中,61例(80%)为女性,中位年龄为62岁。一线治疗后的总缓解率为92.1%,中位无进展生存期为15个月。33例患者胸腔镜滑石粉胸膜固定术的成功率为94%。中位随访时间为35个月。中位总生存期为39个月。1年和3年总生存率分别为86.4%和46.1%。两线序贯治疗策略提高了生存率。这些初步研究结果为携带EGFR突变的NSCLC恶性胸腔积液的新型治疗模式提供了见解。

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