Impact of the extent of surgery and postoperative chemoradiotherapy on recurrence patterns in gastric cancer
- PMID: 20368551
- DOI: 10.1200/JCO.2009.26.9654
Impact of the extent of surgery and postoperative chemoradiotherapy on recurrence patterns in gastric cancer
Abstract
Purpose: The Intergroup 0116 trial has demonstrated that postoperative chemoradiotherapy (CRT) improves survival in gastric cancer. We retrospectively compared survival and recurrence patterns in two phase I/II studies evaluating more intensified postoperative CRT with those from the Dutch Gastric Cancer Group Trial (DGCT) that randomly assigned patients between D1 and D2 lymphadenectomy.
Patients and methods: Survival and recurrence patterns of 91 patients with adenocarcinoma of the stomach who had received surgery followed by radiotherapy combined with fluorouracil and leucovorin (n = 5), capecitabine (n = 39), or capecitabine and cisplatin (n = 47) were analyzed and compared with survival and recurrence patterns of 694 patients from the DGCT (D1, n = 369; D2, n = 325). For both groups, the Maruyama Index of Unresected Disease (MI) was calculated and correlated with survival and recurrence patterns.
Results: With a median follow-up of 19 months in the CRT group, local recurrence rate after 2 years was significantly higher in the surgery only (DGCT) group (17% v 5%; P = .0015). Separate analysis of CRT patients who underwent a D1 dissection (n = 39) versus DGCT-D1 (n = 369) showed fewer local recurrences after chemoradiotherapy (2% v 8%; P = .001), whereas comparison of CRT-D2 (n = 25) versus DGCT-D2 (n = 325) demonstrated no significant difference. CRT significantly improved survival after a microscopically irradical (R1) resection. The MI was found to be a strong independent predictor of survival.
Conclusion: After D1 surgery, the addition of postoperative CRT had a major impact on local recurrence in resectable gastric cancer.
Comment in
-
Postoperative chemoradiotherapy or surgery alone for gastric cancer: the plausibility of the question and pertinence of the answer.J Clin Oncol. 2010 Oct 20;28(30):e615-6; author reply e617-8. doi: 10.1200/JCO.2010.30.8023. Epub 2010 Aug 23. J Clin Oncol. 2010. PMID: 20733136 No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials