Intraperitoneal hyperthermic perfusion with mitomycin C for colorectal cancer with peritoneal metastases |
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Authors: | Dr. Schlomo Schneebaum MD Mark W. Arnold MD Alfred Staubus PhD Donn C. Young PhD David Dumond BS Edward W. Martin Jr MD |
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Affiliation: | (1) From the Division of Surgical Oncology, Department of Surgery, The Ohio State University Hospitals, Columbus, Ohio, USA;(2) Department of Surgery, The Ohio State University Hospitals, Columbus, Ohio, USA;(3) Department of Pharmacology, The Ohio State University Hospitals, Columbus, Ohio, USA;(4) Department of Circulation Technology, The Ohio State University Hospitals, Columbus, Ohio, USA;(5) Department of Biostatistics, The Arthur G. James Cancer Hospital and Research Institute, Columbus, Ohio, USA |
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Abstract: | Background: Intraperitoneal (i.p.) metastases pose a special problem for surgical treatment because of their multiplicity and microscopic size. This study was designed to examine the feasibility and safety of i.p. hyperthermic perfusion (IPHP) with mitomycin C (MMC) for treating recurrent colorectal cancer. Methods: Fifteen patients with metastatic colon cancer were treated. All patients underwent cytoreductive procedures leaving only residual i.p. metastases <1 cm in diameter. All patients had received prior systemic chemotherapy, but their disease had progressed. Intraperitoneal chemotherapy was administered through three large catheters (28 French) using a closed system of two pumps, a heat exchanger, and two filters. After the patient’s abdominal temperature reached 41°C, 45–60 mg of MMC was circulated intraperitoneally for 1 h. Results: The majority of patients had various anastomoses: small bowel (n=11), large bowel (n=5), and urologic (n=5). No anastomotic complications occurred in any of the patients. One patient experienced severe systemic MMC toxicity, which caused cytopenia and respiratory depression. In all patients the carcinoembryonic antigen (CEA) level decreased after surgery and IPHP. Median follow-up was 10 months, and recurrence was defined as an elevation in CEA level. Disease recurred in three patients within 5 months, and disease recurred in seven other patients over the next 3 months; one patient remains clinically free of disease after 8 months. Conclusion: Our data suggest that IPHP is a safe palliative method of treatment for patients with peritoneal carcinomatosis. The median patient response duration of 6 months may warrant consideration of a repeat IPHP procedure at that time. Presented at the 46th Annual Cancer Symposium of The Society of Surgical Oncology, Los Angeles, March 18–21, 1993. |
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Keywords: | Intraperitoneal chemotherapy Hyperthermia Colorectal cancer Peritoneal metastasis Mitomycin C |
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