Hyperthermic intraperitoneal chemoperfusion as a component of multimodality therapy for ovarian and primary peritoneal cancer

被引:13
|
作者
Magge, Deepa [1 ]
Ramalingam, Lekshmi [1 ]
Shuai, Yongli [2 ]
Edwards, Robert P. [1 ,3 ]
Pingpank, James F. [1 ]
Ahrendt, Steven S. [1 ]
Holtzman, Matthew P. [1 ]
Zeh, Herbert J. [1 ]
Bartlett, David L. [1 ]
Choudry, Haroon A. [1 ]
机构
[1] Univ Pittsburgh, Div Surg Oncol, Koch Reg Perfus Ctr, 5150 Ctr Ave,Suite 424, Pittsburgh, PA 15232 USA
[2] Univ Pittsburgh, Inst Canc, Biostat Facil, 5150 Ctr Ave,Suite 424, Pittsburgh, PA 15232 USA
[3] Univ Pittsburgh, Dept Obstet & Gynecol, 5150 Ctr Ave,Suite 424, Pittsburgh, PA 15232 USA
关键词
cisplatin; cytoreductive surgery; HIPEC multimodality; ovarian cancer; primary peritoneal cancer; PHASE-III TRIAL; CYTOREDUCTIVE SURGERY; NEOADJUVANT CHEMOTHERAPY; CISPLATIN; SURVIVAL; HIPEC; PACLITAXEL; CARCINOMATOSIS; CARBOPLATIN; MORBIDITY;
D O I
10.1002/jso.24666
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives: The role of hyperthermic intraperitoneal chemoperfusion (HIPEC) in the multimodality treatment of ovarian peritoneal metastases (OPM) and primary peritoneal cancer (PPC) remains controversial. We hypothesized that cytoreductive surgery (CRS) and HIPEC would provide meaningful survival benefit without excessive morbidity. Methods: We reviewed clinicopathologic and perioperative data following 96 CRS-HIPEC procedures for primary or recurrent OPM and PPC. Kaplan-Meier survival curves and multivariate Cox-regression models identified prognostic factors affecting oncologic outcomes. Results: CRS-HIPEC was mostly performed for recurrent disease (56.3%) and high-grade serous carcinoma (72.9%). Platinum-based systemic chemotherapy was administered to 89.5% of patients, with 75.5% having platinum-sensitive disease at CRS-HIPEC. Complete macroscopic resection was achieved in 70.8% of patients. Clavien-Dindo grade 3/4 morbidity occurred in 23.4% of patients; three patients died within 60-days postoperatively. Median overall survival from diagnosis of peritoneal metastases and CRS-HIPEC was 78 and 38 months, respectively. Completeness of cytoreduction, pathologic subtype, and 30-day morbidity were independent predictors of survival in multiple regression analysis. Conclusions: Our study demonstrates promising survival data and supports the role of HIPEC in the multimodality treatment algorithm for primary or recurrent OPM and PPC. However definite indications and timing of HIPEC need to be clarified by prospective studies.
引用
收藏
页码:320 / 328
页数:9
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