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[Continuous hyperthermic peritoneal perfusion (CHPP) therapy in advanced gastric cancer]
H Suzuki1, K Miyagishima, F Gasa
1Second Dept. of Surgery, Hirosaki University School of Medicine.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|August 1, 1991
Summary
Increasing chemotherapy perfusion pump (CHPP) infusion rates for gastric cancer did not significantly alter drug concentrations but did raise intraperitoneal temperatures. Higher infusion rates may improve hyperthermia effectiveness in CHPP therapy.
Area of Science:
- Oncology
- Pharmacology
- Surgical Oncology
Context:
- Advanced gastric cancer treatment often involves hyperthermia and chemotherapy.
- Chemotherapy perfusion pump (CHPP) therapy is used to deliver heated chemotherapy intraperitoneally.
- Maintaining optimal intraperitoneal temperature is crucial for CHPP efficacy.
Purpose:
- To evaluate the effect of increased infusion rates on intraperitoneal temperature and drug concentrations during CHPP for advanced gastric cancer.
- To determine if higher infusion rates improve the therapeutic temperature range within the peritoneal cavity.
- To assess systemic drug absorption (CDDP and MMC) at different infusion rates.
Summary:
- CHPP therapy for advanced gastric cancer used cisplatin (CDDP) and mitomycin C (MMC) in warmed saline.
- Increasing the infusion rate from 200 ml/min to 400 ml/min raised intraperitoneal temperature but did not consistently reach effective ranges.
- Maximal plasma concentrations of CDDP and MMC were not significantly different between the two infusion rates.
- Portal venous MMC concentrations were higher than peripheral venous concentrations, but the difference was less pronounced than in animal studies.
Impact:
- Higher CHPP infusion rates can increase intraperitoneal temperatures, potentially enhancing hyperthermia's effect.
- Systemic absorption of CDDP and MMC remains low and is not significantly affected by the tested infusion rate increase.
- Findings suggest a need for further optimization of CHPP protocols to achieve consistent therapeutic temperatures and minimize systemic exposure.