Effect of neoadjuvant chemotherapy on postoperative morbidity and mortality in patients with locally advanced gastric cancer
Author(s) -
Ahn H. S.,
Jeong S.H.,
Son Y. G.,
Lee H.J.,
Im S.A.,
Bang Y.J.,
Kim H.H.,
Yang H.K.
Publication year - 2014
Publication title -
british journal of surgery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.202
H-Index - 201
eISSN - 1365-2168
pISSN - 0007-1323
DOI - 10.1002/bjs.9632
Subject(s) - medicine , folinic acid , oxaliplatin , chemotherapy , neoadjuvant therapy , regimen , surgery , cancer , cohort , fluorouracil , oncology , colorectal cancer , breast cancer
Background Neoadjuvant chemotherapy has been shown to improve the rate of complete ( R0 ) resection and downstaging in patients with localized gastric cancer. There are few reports, however, regarding its impact on postoperative morbidity and mortality. The aims of this study were to analyse complication and mortality rates after neoadjuvant chemotherapy using a modified regimen of folinic acid, 5‐fluorouracil and oxaliplatin ( mFOLFOX6 ) for locally advanced gastric cancer ( AGC ), compared with rates in patients who underwent surgery without neoadjuvant chemotherapy. Methods Data were collected from patients with AGC enrolled in a phase II trial of four cycles of neoadjuvant mFOLFOX6 followed by surgery, between January 2005 and June 2008 at two of three institutions, and compared with those from a cohort of patients with AGC who underwent surgery alone at one of the institutions in 2006. Results Among 51 patients who received neoadjuvant chemotherapy, there were no deaths and a morbidity rate of 24 per cent after surgery. Comparison of 48 patients in one institution who received neoadjuvant chemotherapy with 92 patients who had surgery alone in the same institution showed no increase in postoperative morbidity (23 versus 29 per cent; P = 0·417). Combined resection was the only risk factor for postoperative morbidity after neoadjuvant chemotherapy. Conclusion Neoadjuvant chemotherapy with mFOLFOX is a safe treatment for patients with localized AGC , and does not increase postoperative morbidity or mortality.
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