A Randomized, Double-Blind, Phase 2 Trial of Platinum Therapy Plus Etoposide With or Without Concurrent Vandetanib (ZD6474) in Patients With Previously Untreated Extensive-Stage Small Cell Lung Cancer: Hoosier Cancer Research Network LUN06-113

被引:29
作者
Sanborn, Rachel E. [1 ]
Patel, Jyoti D. [2 ]
Masters, Gregory A. [3 ]
Jayaram, Nagesh [4 ]
Stephens, Anthony [5 ]
Guarino, Michael [3 ]
Misleh, Jamal [3 ]
Wu, Jingwei [6 ]
Hanna, Nasser [7 ]
机构
[1] Providence Canc Ctr, Earle A Chiles Res Inst, 4805 Northeast Glisan,2N35, Portland, OR 97213 USA
[2] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Christiana Care Hlth Syst, Newark, DE USA
[4] Southeastern Med Oncol, Jacksonville, NC USA
[5] Oncol Hematol Associates Southwest Indiana, Newburgh, IN USA
[6] Indiana Univ, Dept Biostat, Indianapolis, IN 46204 USA
[7] Indiana Univ, Simon Canc Ctr, Indianapolis, IN 46204 USA
关键词
carboplatin; cisplatin; etoposide; small cell lung cancer; vandetanib; II TRIAL; BEVACIZUMAB; CHEMOTHERAPY; CISPLATIN; PACLITAXEL; IRINOTECAN; CARBOPLATIN; COMBINATION; INTERGROUP; SORAFENIB;
D O I
10.1002/cncr.30287
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: This randomized, double-blind, phase 2 trial evaluated whether the addition of vandetanib to platinum plus etoposide for previously untreated extensive-stage small cell lung cancer (SCLC) prolonged the time to disease progression in comparison with chemotherapy alone. METHODS: Patients with previously untreated extensive-stage SCLC received platinum (cisplatin or carboplatin) with etoposide in combination with vandetanib (100mg daily) or a placebo for up to 4 total cycles (no maintenance therapy). An initial safety run-in phase was conducted with the first 6 patients enrolled; all these patients received vandetanib with cisplatin and etoposide. With an overall sample size of 68 patients, the study had 80% power to detect a 3-month difference in the time to progression (TTP) from 4 to 7 months (significance level,. 10 [1-sided log-rank test]). RESULTS: Seventy-four patients were enrolled between April 2008 and May 2013. Thirty-three patients were ultimately randomized to each arm. The baseline characteristics were well balanced, and the median number of treatment cycles was 4 for each arm. Thirty-one patients in each arm were evaluable for TTP; the median TTP was 5.62 months with vandetanib and 5.68 months with the placebo (P=.9518). The median overall survival was 13.24 months with vandetanib and 9.23 months with the placebo (P=.4577; 33 evaluable patients in each arm). Nonhematologic toxicity was increased with vandetanib versus the placebo. No correlation was seen between vascular endothelial growth factor polymorphisms and outcomes. CONCLUSIONS: The addition of vandetanib to platinum and etoposide did not improve outcomes for patients with newly diagnosed extensive-stage SCLC. Toxicity was increased in comparison with chemotherapy alone. (C) 2016 American Cancer Society.
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收藏
页码:303 / 311
页数:9
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