Outcome Data of Patients with Peritoneal Carcinomatosis from Gastric Origin Treated by a Strategy of Bidirectional Chemotherapy Prior to Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy in a Single Specialized Center in Japan

被引:91
作者
Canbay, Emel [1 ]
Mizumoto, Akiyoshi [2 ]
Ichinose, Masumi [2 ]
Ishibashi, Haruaki [2 ]
Sako, Shouzou [1 ]
Hirano, Masamitsu [2 ]
Takao, Nobuyuki [2 ]
Yonemura, Yutaka [1 ,2 ,3 ]
机构
[1] Tokushu Kai Hosp, Dept Gen Surg, NPO Support Peritoneal Disseminat Treatment, Osaka, Japan
[2] Kusatsu Gen Hosp, Dept Gen Surg, Kusatsu, Japan
[3] Kishiwada Tokushukai Hosp, Dept Gen Surg, Osaka, Japan
关键词
NEOADJUVANT TREATMENT; PHASE-II; CANCER; DISSEMINATION; PLUS; S-1;
D O I
10.1245/s10434-013-3443-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Management of peritoneal disseminated gastric cancer (GC) remains a challenging problem. The purpose of our study was to evaluate the outcome of bidirectional induction chemotherapy [bidirectional intraperitoneal and systemic induction chemotherapy (BIPSC)] in patients with peritoneal carcinomatosis (PC) arising from GC who underwent cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). Patients and Methods. Overall, 194 patients with PC arising from GC were treated with BIPSC comprising intraperitoneal docetaxel at a dose of 20 mg/m(2) and cisplatin at a dose of 30 mg/m(2) followed by four cycles of oral S-1 at a dose of 60 mg/m(2). CRS and HIPEC were performed in responders to BIPSC. Results. Of these 194 patients, 152 (78.3 %) underwent CRS and HIPEC between January 2005 and December 2012. Treatment-related mortality was 3.9 %, and major complications occurred in 23.6 % of patients. The median survival rate was 15.8 months, with 1-, 2-, and 5-year survival rates of 66, 32 and 10.7 %, respectively, in the patients treated with combined treatment. Multivariate analysis identified pathologic response to BIPSC (p = 0.001), low tumor burden [peritoneal cancer index (PCI) <= 6] (p = 0.001), and completeness of CRS (CC-0, CC-1) (p = 0.001) as independent predictors for a better prognosis. Conclusion. As a viable option, BIPSC with CRS and HIPEC for patients with PC arising from GC may be performed safely, with acceptable morbidity and mortality, in a specialized unit. Response to BIPSC, optimal CRS and limited peritoneal dissemination seem to be essential to achieve the best outcomes in these patients.
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收藏
页码:1147 / 1152
页数:6
相关论文
共 24 条
[1]   Does neoadjuvant treatment for gastric cancer patients with positive peritoneal cytology at staging laparoscopy improve survival? [J].
Badgwell, Brian ;
Cormier, Janice N. ;
Krishnan, Sunil ;
Yao, James ;
Staerkel, Gregg A. ;
Lupo, Philip J. ;
Pisters, Peter W. T. ;
Feig, Barry ;
Mansfield, Paul .
ANNALS OF SURGICAL ONCOLOGY, 2008, 15 (10) :2684-2691
[2]   Locoregional treatment of peritoneal carcinomatosis from gastric cancer [J].
Bozzetti, F. ;
Yu, W. ;
Baratti, Dario ;
Kusamura, Shigeki ;
Deraco, Marcello .
JOURNAL OF SURGICAL ONCOLOGY, 2008, 98 (04) :273-276
[3]  
Fujimoto S, 1997, CANCER, V79, P884, DOI 10.1002/(SICI)1097-0142(19970301)79:5<884::AID-CNCR3>3.0.CO
[4]  
2-C
[5]   Neoadjuvant Intraperitoneal and Systemic Chemotherapy for Gastric Cancer Patients with Peritoneal Dissemination [J].
Fujiwara, Yoshiyuki ;
Takiguchi, Shuji ;
Nakajima, Kiyokazu ;
Miyata, Hiroshi ;
Yamasaki, Makoto ;
Kurokawa, Yukinori ;
Okada, Kaoru ;
Mori, Masaki ;
Doki, Yuichiro .
ANNALS OF SURGICAL ONCOLOGY, 2011, 18 (13) :3726-3731
[6]   Cytoreductive surgery and intraperitoneal chemohyperthermia for peritoneal carcinomaiosis arising from gastric cancer [J].
Glehen, O ;
Schreiber, V ;
Cotte, E ;
Sayag-Beaujard, AC ;
Osinsky, D ;
Freyer, G ;
François, Y ;
Vignal, J ;
Gilly, FN .
ARCHIVES OF SURGERY, 2004, 139 (01) :20-26
[7]   Randomized comparison between chemotherapy plus best supportive care with best supportive care in advanced gastric cancer [J].
Glimelius, B ;
Ekstrom, K ;
Hoffman, K ;
Graf, W ;
Sjoden, PO ;
Haglund, U ;
Svensson, C ;
Enander, LK ;
Linne, T ;
Sellstrom, H ;
Heuman, R .
ANNALS OF ONCOLOGY, 1997, 8 (02) :163-168
[8]   Cytoreductive surgery with intraperitoneal hyperthermic chemotherapy for advanced gastric cancer [J].
Hall, JY ;
Loggie, BW ;
Shen, P ;
Beamer, S ;
Case, LD ;
McQuellon, R ;
Geisinger, KR ;
Levine, EA .
JOURNAL OF GASTROINTESTINAL SURGERY, 2004, 8 (04) :454-463
[9]   Phase II Study of Single Intraperitoneal Chemotherapy Followed by Systemic Chemotherapy for Gastric Cancer with Peritoneal Metastasis [J].
Imano, Motohiro ;
Yasuda, Atsushi ;
Itoh, Tatsuki ;
Satou, Takao ;
Peng, Ying-Feng ;
Kato, Hiroaki ;
Shinkai, Masayuki ;
Tsubaki, Masahiro ;
Chiba, Yasutaka ;
Yasuda, Takushi ;
Imamoto, Haruhiko ;
Nishida, Shozo ;
Takeyama, Yoshifumi ;
Okuno, Kiyokata ;
Furukawa, Hiroshi ;
Shiozaki, Hitoshi .
JOURNAL OF GASTROINTESTINAL SURGERY, 2012, 16 (12) :2190-2196
[10]   Phase II study of weekly intravenous and intraperitoneal paclitaxel combined with S-1 for advanced gastric cancer with peritoneal metastasis [J].
Ishigami, H. ;
Kitayama, J. ;
Kaisaki, S. ;
Hidemura, A. ;
Kato, M. ;
Otani, K. ;
Kamei, T. ;
Soma, D. ;
Miyato, H. ;
Yamashita, H. ;
Nagawa, H. .
ANNALS OF ONCOLOGY, 2010, 21 (01) :67-70