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Safety of intraperitoneal Mitomycin C versus intraperitoneal oxaliplatin in patients with peritoneal carcinomatosis of colorectal cancer undergoing cytoreductive surgery and HIPEC
Authors:W.J. van Eden  N.F.M. Kok  K. Woensdregt  A.D.R. Huitema  H. Boot  A.G.J. Aalbers
Affiliation:1. Department of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands;2. Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute, Amsterdam, The Netherlands;3. Department of Clinical Pharmacy, University Medical Centre Utrecht, Utrecht, The Netherlands;4. Department of Medical Oncology & Gastroenterology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
Abstract:

Background

Colorectal peritoneal carcinomatosis (PC) is commonly treated with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). There is an ongoing international debate about which intraperitoneal chemotherapeutic agent is preferred, Mitomycin C (MMC) or oxaliplatin. We questioned whether the type of chemotherapeutic agent influenced postoperative complication rates or short-term survival.

Methods

In this retrospective cohort study patients with colorectal PC who underwent CRS-HIPEC between January 2010 and December 2016 were included. Until March 2014 patients had preferentially been treated with MMC and thereafter with oxaliplatin in an iso-osmotic glucose/electrolyte dialysis (Dianeal®) carrier solution. Main outcomes were postoperative complications, disease free survival (DFS) and overall survival (OS). Survival analyses and multivariable analyses were performed.

Results

One hundred four patients received MMC and 73 patients oxaliplatin. Postoperative complications did not differ between groups (44.2% (MMC) versus 43.8% (oxaliplatin); P = 0.958). Median DFS was 12.5 months (IQR 6.4–32.4) in the MMC-group and 13.1 months (IQR 6.1-NA) in the oxaliplatin-group (P = 0.669). Median OS was 37.2 months (IQR 17.2-NA) in the MMC-group and 29.4 months (IQR 17.0-NA) in the oxaliplatin-group (P = 0.764). The type of chemotherapeutic agent did not influence OS in multivariable analysis (oxaliplatin versus MMC HR 1.09 (95%CI 0.58–2.06)). The HIPEC-phase was shorter for oxaliplatin (median 32 (IQR 31–34) versus 91 min (IQR 90–92) for MMC (P < 0.001)).

Conclusion

Intraperitoneal oxaliplatin reduced the chemoperfusion time when compared to intraperitoneal MMC without adversely influencing complication rates or short-term survival. It may therefore be the preferential drug in CRS-HIPEC procedures for colorectal PC.
Keywords:Colorectal cancer  Peritoneal carcinomatosis  Mitomycin C  Oxaliplatin  HIPEC
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