Early postoperative intraperitoneal chemotherapy with mitomycin C, 5-fluorouracil and cisplatin for advanced gastric cancer

被引:19
作者
Noh, SH
Yoo, CH
Chung, HC
Roh, JK
Shin, DW
Min, JS
机构
[1] Yonsei Univ, Coll Med, Dept Surg, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Dept Internal Med, Seoul 120752, South Korea
[3] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Surg, Seoul, South Korea
关键词
intraperitoneal chemotherapy; gastric cancer; prognosis;
D O I
10.1159/000055292
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The long-term survival of patients who undergo surgery for stage IV gastric cancer is poor, due to metastatic spread of the tumor. Intraperitoneal chemotherapy (IPT) as a possible treatment for peritoneal dissemination has been investigated in a number of different tumors. The aim of this study was to investigate the toxicity and impact of early postoperative IPT on the survival of patients with advanced gastric cancer. Methods: Between 1993 and 1997, a total of 91 patients with stage IV gastric cancer who underwent potentially curative or palliative resection received intraperitoneal mitomycin C before closure of the abdominal wound. 5-Fluorouracil and cisplatin were administered intraperitoneally on postoperative days 1-4, and this was repeated at 4-week intervals. Results: All patients received a median of 3 IPT perfusions. There were 24 (26.4%) postoperative complications and 1 (1.1%) mortality. The most frequent hematologic toxicity (grade 3-4) was leukopenia. The major nonhematologic toxicities (grade 3-4) were emesis and nephrotoxicity. After a median follow-up period of 26 months, 14 patients remain alive without evidence of recurrence, whereas 75 patients died due to recurrence or progression of disease. The median survival period for all 91 patients was 15.4 months. When survival according to the residual tumor was analyzed, median survival was 36.0 months in the R0 (curative resection) group, 20.6 months in the R1 group (margins of resected specimens showing microscopic residual tumor or diameter of each residual tumor less than 3 mm) and 9.0 months in the R2 group (macroscopic residual tumor larger than 3 mm) (p < 0.001). Conclusions: IPT was found to be safe, and it appears to improve the prognosis in patients with minimal residual tumors. However, complete cytoreductive surgery is mandatory for achieving the beneficial effect of IPT. Copyright (C) 2001 S. Karger AG, Basel.
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收藏
页码:24 / 30
页数:7
相关论文
共 31 条
[1]   PHASE-II TRIAL OF POSTOPERATIVE ADJUVANT INTRAPERITONEAL CISPLATIN AND FLUOROURACIL AND SYSTEMIC FLUOROURACIL CHEMOTHERAPY IN PATIENTS WITH RESECTED GASTRIC-CANCER [J].
ATIQ, OT ;
KELSEN, DP ;
SHIU, MH ;
SALTZ, L ;
TONG, W ;
NIEDZWIECKI, D ;
TROCHANOWSKI, B ;
LIN, SL ;
TOOMASI, F ;
BRENNAN, M .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (03) :425-433
[2]   Strategies to decrease the incidence of intra-abdominal recurrence in resectable gastric cancer [J].
Averbach, AM ;
Jacquet, P .
BRITISH JOURNAL OF SURGERY, 1996, 83 (06) :726-733
[3]  
Crookes P, 1997, CANCER, V79, P1767, DOI 10.1002/(SICI)1097-0142(19970501)79:9<1767::AID-CNCR19>3.0.CO
[4]  
2-W
[5]   GASTROINTESTINAL MALIGNANCY - RATIONALE FOR ADJUVANT THERAPY USING EARLY POSTOPERATIVE INTRAPERITONEAL CHEMOTHERAPY [J].
CUNLIFFE, WJ ;
SUGARBAKER, PH .
BRITISH JOURNAL OF SURGERY, 1989, 76 (10) :1082-1090
[6]   Pharmacokinetic problems in peritoneal drug administration: Tissue penetration and surface exposure [J].
Dedrick, RL ;
Flessner, MF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (07) :480-487
[7]  
DEDRICK RL, 1978, CANCER TREAT REP, V62, P1
[8]  
Frasci G, 1994, Clin Oncol (R Coll Radiol), V6, P364, DOI 10.1016/S0936-6555(05)80188-8
[9]  
FUJIMOTO S, 1993, ONCOLOGY, V50, P338
[10]  
Fujimoto S, 1998, CANCER, V85, P529