Nuclear survivin expression: a prognostic factor for the response to taxane–platinum chemotherapy in patients with advanced non-small cell lung cancer

被引:0
作者
Yao-Kuang Wu
Chun-Yao Huang
Mei-Chen Yang
Chou-Chin Lan
Chih-Hsin Lee
Err-Cheng Chan
Kuei-Tien Chen
机构
[1] Taipei Tzu Chi Hospital,Division of Pulmonary Medicine, Department of Internal Medicine
[2] Buddhist Tzu Chi Medical Foundation,School of Medicine
[3] Tzu-Chi University,Department of Medical Biotechnology and Laboratory Science
[4] Chang Gung University,undefined
来源
Medical Oncology | 2014年 / 31卷
关键词
Non-small cell lung cancer; Survivin expression; Platinum–taxane chemotherapy; Paclitaxel; Docetaxel;
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摘要
Survivin, a structurally unique protein expressed in most common human neoplasms, is thought to support cell cycle progression and suppress apoptosis. Survivin expression is highly correlated with advanced non-small cell lung cancer (NSCLC) and poor prognosis. In this retrospective study of banked pathology tissue of patients with advanced NSCLC, we tested for correlations of N-survivin expression in tumor tissues and responsiveness to treatment with platinum-based regimens containing paclitaxel or docetaxel. The 48 patients with NSCLC included 32 (66.7 %) males and 16 (33.3 %) females. Mean age at diagnosis was 59.4 years (range 36–83 years), and median follow-up time was 20.4 months (range 3.4–59.0 months). Patients with high tumor N-survivin expression had significantly better responses to taxane–platinum chemotherapy than those with low tumor N-survivin expression (P < 0.001). Adjusted multivariate modeling found high tumor N-survivin expression to be an independent prognostic factor for a clinical response to chemotherapy (high vs. low, OR 6.14, 95 % CI 1.62–23.29; P = 0.008). Median overall survival differed significantly between those with high tumor N-survivin expression who did/did not respond to chemotherapy and between those with low tumor N-survivin expression who did/did not respond to chemotherapy (P < 0.05). Tumor N-survivin expression shows promise as a predictive biomarker in the chemotherapy setting as a surrogate marker of high proliferation status.
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