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Neoadjuvant chemotherapy with FOLFOX: Improved outcomes in Chinese patients with locally advanced gastric cancer
Author(s) -
Li ZiYu,
Koh Cherry E.,
Bu ZhaoDe,
Wu AiWen,
Zhang LianHai,
Wu XiaoJiang,
Wu Qi,
Zong XiangLong,
Ren Hui,
Tang Lei,
Zhang XiaoPeng,
Li JiYou,
Hu Ying,
Shen Lin,
Ji JiaFu
Publication year - 2011
Publication title -
journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.201
H-Index - 111
eISSN - 1096-9098
pISSN - 0022-4790
DOI - 10.1002/jso.23009
Subject(s) - medicine , folfox , leukopenia , chemotherapy , oncology , cancer , adjuvant , neoadjuvant therapy , surgery , gastroenterology , oxaliplatin , colorectal cancer , breast cancer
Background Although the role of peri‐operative chemotherapy is established in the treatment of locally advanced gastric cancer, the optimal regime remains to be determined. FOLFOX has been used in palliative setting with good response rates but its role in a neoadjuvant setting is not well established. Methods This is a prospective non‐randomized study comparing peri‐operative FOLFOX versus adjuvant FOLFOX in patients with resectable locally advanced gastric cancer. Response to chemotherapy was assessed according to WHO criteria and pathological changes. Kaplan–Meier log rank test was used to calculate and compare survival differences. Results There were 73 patients (neoadjuvant = 36). Complete and partial response was observed in 2 (6%) and 21 (64%) patients, respectively. Four‐year overall survival (OS) in the neoadjuvant arm was 78% versus 51% in the adjuvant arm ( P = 0.031). Subgroup analysis found R0 resection (86% vs. 55%, P = 0.011) and patients with proximal cancers (87% vs. 14%, P < 0.001) to have improved OS. The most common side effect was grade 1–2 leukopenia. There were no grade 3 neuropathies, grade 4 cytopaenias, or treatment related deaths. Conclusion Peri‐operative treatment with FOLFOX shows promise in patients with resectable locally advanced gastric cancer. It warrants further evaluation and should be considered an alternative to peri‐operative ECF. J. Surg. Oncol. 2012; 105:793–799. © 2011 Wiley Periodicals, Inc.