4.7 Article

Lymph Node Status After Neoadjuvant Radiotherapy for Rectal Cancer Is a Biologic Predictor of Outcome

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CANCER
卷 115, 期 23, 页码 5432-5440

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JOHN WILEY & SONS INC
DOI: 10.1002/cncr.24622

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(MeSH): rectal neoplasms; neoadjuvant radiotherapy; adjuvant radiotherapy; adjuvant chemotherapy; SEER program

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资金

  1. American Society of Clinical Oncology Career Development Award

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BACKGROUND: Lymph node (LN) status after surgery for rectal cancer is affected by preoperative radiotherapy. The purpose of this study was to perform a population-based evaluation of the impact of pathologic LN status (ypN) after neoadjuvant radiotherapy on survival. METHODS: Patients undergoing radical resection for rectal adenocarcinoma were identified from the Surveillance Epidemiology and End Results registry (1991-2004). Patient characteristics, overall survival, and cancer-specific survival (CSS) by ypN stage after surgery and use of preoperative or postoperative radiotherapy were compared. RESULTS: Of the 23,809 patients identified, 12,513 received preoperative (n = 5367) or postoperative (n = 7146) radiotherapy and resection. Preoperative patients were more likely to be younger (P < .001) and histopathologically free of detectable nodal metastasis (ypNO) than postoperative (51.8% vs 31.7%, P < .001). Median total numbers of LNs (6 vs 10) and positive LNs (2 vs 3) were lower among preoperative than postoperative (P < .001 for both). OS and CSS were similar among pNO patients. However, on proportional hazards regression, ypN+ stage was associated with an increase in relative risk for death by 21% overall (hazard ratio [HR] = 1.21; 95% confidence interval 1.09-1.35, P < .001) and 23% cancer-specific (HR = 1.23; P = .001) for preoperative compared with postoperative. CONCLUSIONS: Pathologic LN status after neoadjuvant radiotherapy for rectal cancer is a biologic marker of prognosis. Patients who are ypN+ after preoperative are a subgroup of LN positive patients with adverse outcome. These high-risk patients should be targeted for studies of novel multidisciplinary approaches, including expanded chemo- and biologic therapies. Cancer 2009;115:5432-40. (C) 2009 American Cancer Society.

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