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Hyperthermic intraperitoneal chemotherapy with cisplatin and paclitaxel in advanced ovarian cancer: a multicenter prospective observational study
Authors:Federico Coccolini  Luca Campanati  Fausto Catena  Valentina Ceni  Marco Ceresoli  Jorge Jimenez Cruz  Marco Lotti  Stefano Magnone  Josephine Napoli  Diego Rossetti  Pierandrea De Iaco  Luigi Frigerio  Antonio Pinna  Ingo Runnebaum  Luca Ansaloni
Affiliation:1.Unit of General Surgery I, Papa Giovanni XXIII Hospital, Bergamo, Italy.;2.Unit of General, Emergency and Transplant Surgery, Sant''Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.;3.Unit of Gynecologic Surgery, Papa Giovanni XXIII Hospital, Bergamo, Italy.;4.Unit of Gynaecology, Jena University Hospital, Jena, Germany.;5.University of Hawaii at Manoa, Honolulu, HI, USA.;6.Unit of Gynecologic Oncology, Sant''Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Abstract:

Objective

Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) have been recently reported with favorable oncological outcomes as treatment of advanced epithelial ovarian cancer (EOC). The aim of this study was to demonstrate the feasibility of CRS+HIPEC with cisplatin and paclitaxel for the treatment of advanced EOC.

Methods

This is a prospective observational study of 54 patients, from April 2007 to October 2013, with primary or recurrent peritoneal carcinomatosis due to EOC. The mean age was 54.51±9.34. Thirty patients (59%) had primary EOC, and 24 patients (41%) had recurrent disease.

Results

Mean peritoneal cancer index was 10.11 (range, 0 to 28), complete cytoreduction (CC0) was achieved for 47 patients (87%), CC1 for seven patients (13%). Patients with suboptimal cytoreduction (CC2 and CC3) were not included in the study. The mean stay in intensive care unit was 4.73±5.51 days and the mean hospitalization time was 24.0±10.03 days. We did not observe any intraoperative death. Seven patients (13%) required additional operations. Three patients (5.6%) died within 30 days from the procedure. Severe complications were seen in 19 patients (35.2%). During the follow-up period, disease recurred in 33 patients (61.1%); the median disease-free survival time was 12.46 months and the median overall survival time was 32.91 months.

Conclusion

CRS+HIPEC with cisplatin and paclitaxel for advanced EOC is feasible with acceptable morbidity and mortality. Additional follow-up and further studies are needed to determine the effects of HIPEC on long term survival.
Keywords:Cisplatin   Disease-free Survival   Ovarian Neoplasms   Paclitaxel   Prospective studies
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