Originally published as JCO Early Release 10.1200/JCO.2005.04.6110 on June 12 2006
Journal of Clinical Oncology, Vol 24, No 19 (July 1), 2006: pp. 2998-3006
© 2006 American Society of Clinical Oncology.
Postoperative Radiotherapy for Stage II or III NonSmall-Cell Lung Cancer Using the Surveillance, Epidemiology, and End Results Database
Brian E. Lally,
Daniel Zelterman,
Joseph M. Colasanto,
Bruce G. Haffty,
Frank C. Detterbeck,
Lynn D. Wilson
From the Department of Radiation Oncology, Wake Forest University School of Medicine, Winston-Salem, NC; Division of Biostatistics, Yale University School of Public Health; Departments of Therapeutic Radiology and Surgery, Yale University School of Medicine, New Haven, CT; and the Department of Radiation Oncology, University of Medicine and Dentistry of New JerseyRobert Wood Johnson Medical School, Piscataway, NJ
Address reprint requests to Brian E. Lally, MD, Wake Forest University School of Medicine, Department of Radiation Oncology, Medical Center Blvd, Winston-Salem, NC 27157-1030; e-mail: blally{at}wfubmc.edu
PURPOSE: To investigate the association between survival and postoperative radiotherapy (PORT) in patients with resected nonsmall-cell lung cancer (NSCLC).
PATIENTS AND METHODS: Within the Surveillance, Epidemiology, and End Results database, we selected patients with stage II or III NSCLC who underwent a lobectomy or pneumonectomy. Only those patients coded as receiving PORT or observation were included. To account for perioperative mortality, we excluded patients who survived less than 4 months. As a result of our inclusion criteria, we selected a total of 7,465 patients, with a median follow-up time of 3.5 years for patients still alive.
RESULTS: Predictors for the use of PORT included age less than 50 years, higher American Joint Committee on Cancer stage, T3-4 tumor stage, larger tumor size, advanced node stage, greater number of lymph nodes involved, and a ratio of lymph nodes involved to lymph nodes sampled approaching 1.00. On multivariate analysis, older age, T3-4 tumor stage, N2 node stage, male sex, fewer sampled lymph nodes, and greater number of involved lymph nodes had a negative impact on survival. The use of PORT did not have a significant impact on survival. However, in subset analysis for patients with N2 nodal disease (hazard ratio [HR] = 0.855; 95% CI, 0.762 to 0.959; P = .0077), PORT was associated with a significant increase in survival. For patients with N0 (HR = 1.176; 95% CI, 1.005 to 1.376; P = .0435) and N1 (HR = 1.097; 95% CI, 1.015 to 1.186; P = .0196) nodal disease, PORT was associated with a significant decrease in survival.
CONCLUSION: In a population-based cohort, PORT use is associated with an increase in survival in patients with N2 nodal disease but not in patients with N1 and N0 nodal disease.
Supported by National Institutes of Health Grant No. 1T32CA113267-01, TRADONC Fellowship (B.E.L.).
Presented at the 47th Annual Meeting of the American Society for Therapeutic Radiology and Oncology, Denver, CO, October 16-20, 2005.
Authors disclosures of potential conflicts of interest and author contributions are found at the end of this article.

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