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Cytoreduction and HIPEC in The Netherlands: Nationwide Long-term Outcome Following the Dutch Protocol
Authors:Anke M. J. Kuijpers MD  Boj Mirck MD  Arend G. J. Aalbers MD  Simon W. Nienhuijs MD   PhD  Ignace H. J. T. de Hingh MD   PhD  Martinus J. Wiezer MD   PhD  Bert van Ramshorst MD   PhD  Robert J. van Ginkel MD   PhD  Klaas Havenga MD   PhD  Andreas J. Bremers MD   PhD  Johannes H. W. de Wilt MD   PhD  Elisabeth A. te Velde MD   PhD  Vic J. Verwaal MD   PhD
Affiliation:1. Department of Surgical Oncology, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
2. Department of Surgery, Catharina Hospital Eindhoven, Eindhoven, The Netherlands
3. Department of Surgery, Sint Antonius Hospital Nieuwegein, Nieuwegein, The Netherlands
4. Department of Surgery, University Medical Center Groningen, Groningen, The Netherlands
5. Department of Surgery, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands
6. Department of Surgery, VU Medical Centre Amsterdam, Amsterdam, The Netherlands
Abstract:

Purpose

This nationwide study evaluated results of cytoreductive surgery (CRS) combined with hyperthermic intraperitoneal chemotherapy (HIPEC) for peritoneal metastasis of colorectal origin in the Netherlands following a national protocol.

Methods

In a multi-institutional study prospective databases of patients with peritoneal carcinomatosis (PC) from colorectal cancer and pseudomyxoma peritonei (PMP) treated according to the Dutch HIPEC protocol, a uniform approach for the CRS and HIPEC treatment, were reviewed. Primary end point was overall survival and secondary end points were surgical outcome and progression-free survival.

Results

Nine-hundred sixty patients were included; 660 patients (69 %) were affected by PC of colorectal carcinoma and the remaining suffered from PMP (31 %). In 767 procedures (80 %), macroscopic complete cytoreduction was achieved. Three-hundred and thirty one patients had grade III–V complications (34 %). Thirty-two patients died perioperatively (3 %). Median length of hospital stay was 16 days (range 0–166 days). Median follow-up period was 41 months (95 % confidence interval (CI), 36–46 months). Median progression-free survival was 15 months (95 % CI 13–17 months) for CRC patients and 53 months (95 % CI 40–66 months) for PMP patients. Overall median survival was 33 (95 % CI 28–38 months) months for CRC patients and 130 months (95 % CI 98–162 months) for PMP patients. Three- and five-year survival rates were 46 and 31 % respectively in case of CRC patients and 77 and 65 % respectively in case of PMP patients.

Conclusions

The results underline the safety and efficacy of cytoreduction and HIPEC for PC from CRC and PMP. It is assumed the uniform Dutch HIPEC protocol was beneficial.
Keywords:
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