4.5 Article

Comparative effectiveness of neoadjuvant chemoradiotherapy versus chemotherapy alone followed by surgery for patients with stage IIIA non-small cell lung cancer

Journal

LUNG CANCER
Volume 88, Issue 3, Pages 267-274

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.lungcan.2015.03.015

Keywords

NSCLC; Comparative effectiveness; Radiotherapy; Combined modality therapy

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Objectives: The optimal neoadjuvant therapy prior to surgical resection of stage MA non-small cell lung cancer (NSCLC) is controversial, as data support both preoperative chemoradiotherapy (N-CRT) and chemotherapy (N-CTX). We evaluated the comparative effectiveness of N-CRT versus N-CTX in stage IIIA patients in the National Cancer Database (NCDB). Methods: Patients in the NCDB with stage IIIA NSCLC treated with N-CRT or N-CTX and surgery between 2003 and 2005 were analyzed. Outcomes included overall survival (OS), residual nodal disease (RND), any adverse pathologic features (APF = RND or positive margins), and 30-day postoperative mortality (POPM). The survival impact of post-operative radiotherapy (PORT) after N-CTX was also investigated. Results: The cohort consisted of 1076 patients: 700 (65%) underwent N-CRT. The 5-year OS for the entire cohort was 39% (39.2% N-CRT vs. 38.6% N-CTX, p = NS). On multivariable regression, there was no difference in OS between N-CRT versus N-CTX (p = 0.70). However, N-CRT was associated with a lower independent risk of RND (odds ratio, OR, 0.75, p = 0.02) and a lower risk of APF (OR 0.67, p = 0.0023). Among N-CTX patients, PORT was associated with inferior survival in patients without APF (hazard ratio 1.68, p = 0.01) but not with APF. N-CRT did not increase early POPM, readmission rates, or length of stay. Conclusion: There was no difference in overall survival between these two strategies, although N-CRT was associated with improved pathologic outcomes. These data support either treatment approach, but early surgical consultation is critical to ensure operability. The indications for PORT in patients without adverse pathologic factors require further investigation. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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