Hyperthermic Intraperitoneal Chemotherapy (HIPEC) at the Time of Primary Curative Surgery in Patients with Colorectal Cancer at High Risk for Metachronous Peritoneal Metastases

被引:39
作者
Baratti, Dario [1 ]
Kusamura, Shigeki [1 ]
Iusco, Domenico [2 ]
Gimondi, Silvia [3 ]
Pietrantonio, Filippo [4 ]
Milione, Massimo [5 ]
Guaglio, Marcello [6 ]
Bonomi, Serena [2 ]
Grassi, Antonio [2 ]
Virzi, Salvatore [2 ]
Leo, Ermanno [6 ]
Deraco, Marcello [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Peritoneal Malignancy Program, Milan, Italy
[2] AUSL Bologna, Bentivoglio Hosp, Gen Surg Unit, Bologna, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Dept Haematol, Milan, Italy
[4] Fdn IRCCS Ist Nazl Tumori, Dept Oncol, Milan, Italy
[5] Fdn IRCCS Ist Nazl Tumori, Dept Pathol, Milan, Italy
[6] Fdn IRCCS Ist Nazl Tumori, Colorectal Canc Unit, Milan, Italy
关键词
SYSTEMIC CHEMOTHERAPY; CYTOREDUCTIVE SURGERY; RANDOMIZED-TRIAL; COLON-CANCER; CARCINOMATOSIS; SURVIVAL; 5-FLUOROURACIL; LEUCOVORIN; MANAGEMENT; THERAPY;
D O I
10.1245/s10434-016-5488-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC) are maximally effective in early-stage colorectal cancer peritoneal metastases (CRC-PM); however, the use of HIPEC to treat subclinical-stage PM remains controversial. This prospective two-center study assessed adjuvant HIPEC in CRC patients at high risk for metachronous PM (www.clinicaltrials.gov NCT02575859). During 2006-2012, a total of 22 patients without systemic metastases were prospectively enrolled to receive HIPEC simultaneously with curative surgery, plus adjuvant systemic chemotherapy (oxaliplatin/irinotecan-containing +/- biologics), based on primary tumor-associated criteria: resected synchronous ovarian (n = 2) or minimal peritoneal (n = 6) metastases, primaries directly invading other organs (n = 4) or penetrating the visceral peritoneum (n = 10). A control group retrospectively included 44 matched (1:2) patients undergoing standard treatments and no HIPEC during the same period. The cumulative PM incidence was calculated in a competing-risks framework. Patient characteristics were comparable for all groups. Median follow-up was 65.2 months [95 % confidence interval (CI) 50.9-79.5] in the HIPEC group and 34.5 months (95 % CI 21.1-47.9) in the control group. The 5-year cumulative PM incidence was 9.3 % in the HIPEC group and 42.5 % in the control group (p = 0.004). Kaplan-Meier estimated 5-year overall survival (OS) was 81.3 % in the HIPEC group versus 70.0 % in the control group (p = 0.047). No operative death occurred. Grade 3-4 [National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4] morbidity rates were 18.2 % in the HIPEC group and 25 % in controls (p = 0.75). At multivariate analysis, HIPEC correlated to lower PM cumulative incidence [hazard ratio (HR) 0.04, 95 % CI 0.01-0.31; p = 0.002], and better OS (HR 0.25, 95 % CI 0.07-0.89; p = 0.039) and progression-free survival (HR 0.31, 95 % CI 0.11-0.85; p = 0.028). Adjuvant HIPEC may benefit CRC patients at high-risk for peritoneal failure. These results warrant confirmation in phase III trials.
引用
收藏
页码:167 / 175
页数:9
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