A population-based comparative effectiveness study of chemoradiation regimens and sequences in stage III non-small cell lung cancer

被引:10
作者
Harris, Jeremy P. [1 ]
Patel, Manali I. [2 ]
Loo, Billy W. [1 ,3 ]
Wakelee, Heather A. [2 ,3 ]
Diehn, Maximilian [1 ,3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Dept Radiat Oncol, 875 Blake Wilbur Dr,MC 5847, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Oncol, 269 Campus Dr, Stanford, CA 94305 USA
[3] Stanford Canc Inst, 265 Campus Dr,Ste G2103, Stanford, CA 94305 USA
[4] Inst Stem Cell Biol & Regenerat Med, 265 Campus Dr,3rd Floor, Stanford, CA 94305 USA
关键词
Non-small cell lung cancer; Chemoradiation; Comparative effectiveness research; Platinum-doublet chemotherapy; SEER-Medicare; RANDOMIZED PHASE-III; CONCURRENT CHEMORADIOTHERAPY; CONSOLIDATION CHEMOTHERAPY; THORACIC RADIOTHERAPY; PROPORTIONAL-HAZARDS; COMORBIDITY INDEX; CISPLATIN; CARBOPLATIN; PACLITAXEL; RADIATION;
D O I
10.1016/j.lungcan.2017.03.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: In patients receiving concurrent chemoradiation for locally advanced non-small cell lung cancer (NSCLC), consolidation chemotherapy is frequently given even though several randomized trials have failed to show a benefit. We explored the potential benefits of consolidation chemotherapy using a population-based comparative effectiveness approach. Materials and methods: Surveillance. Epidemiology, and End Results-Medicare was used to identify patients with Stage III NSCLC aged >= 65 and diagnosed 2002-2009. We selected patients who received concurrent chemoradiotherapy and determined whether they were (concurrent-consolidation) or were not (concurrent-alone) treated with consolidation chemotherapy. Outcomes were overall and cancer specific survival using a conditional landmark analysis approach. Results: 1688 patients treated with concurrent-alone or concurrent-consolidation were identified with a median follow up of 29 months. Choice of chemotherapy agents did not correlate with outcome. For concurrent-consolidation versus concurrent-alone, the median overall survival was 21 months versus 18 months, respectively (log-rank p = 0.008) and the median cancer specific survival was 23 months versus 19 months, respectively (log-rank p = 0.03). On multivariate analysis, concurrent-consolidation remained associated with improved overall survival (HR 0.85, p = 0.04), and there was a trend for improved cancer specific survival (HR 0.87, p= 0.12). Inverse probability of treatment weighting using propensity scores demonstrated similar findings. Importantly, the benefit of concurrent-consolidation held only for patients treated with carboplatin-taxane but not with cisplatin-etoposide. Conclusion: Survival outcomes were similar among the five most commonly employed platinum-based doublets. We found that patients receiving cisplatin during radiation do not appear to benefit from additional chemotherapy. However, for patients receiving carboplatin, consolidation chemotherapy was associated with improved overall and cancer specific survival. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 182
页数:10
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