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

被引:16
作者
Lin, Jian-Bo [1 ]
Lai, Fan-Cai [1 ]
Li, Xu [1 ]
Tu, Yuan-Rong [2 ]
Lin, Min [2 ]
Qiu, Min-Lian [1 ]
Luo, Rong-Gang [1 ]
Liu, Bo [1 ]
Lin, Jing-Wei [2 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Thorac Surg, Fuzhou 350005, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Lung Canc Ctr, Fuzhou, Peoples R China
关键词
Epithelial growth factor receptor; malignant pleural effusion; non-small-cell lung cancer; pleurodesis; targeted therapy; ADENOCARCINOMA; TALC; EGFR; CHEMOTHERAPY; PLEURODESIS; GEFITINIB;
D O I
10.1080/1061186X.2016.1200590
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 (250mg/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.
引用
收藏
页码:119 / 124
页数:6
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