Perfusion of the peritoneal cavity with chemotherapy agents under hyperther
mic conditions has been utilized by several investigators in the treatment
of intra-abdominal malignancies. Based on the concept that hyperthermia may
potentiate the cytotoxic effects of chemotherapeutic agents, we embarked o
n a clinical trial of two-stage peritoneal chemotherapy for patients with p
rimary peritoneal mesothelioma, a neoplasm unresponsive to traditional syst
emic chemotherapeutic regimens. In stage I, patients underwent surgical deb
ulking of ross disease and placement of an intraperitoneal infusion cathete
r, through which intraperitoneal chemotherapy was administered for four mon
ths. Stage II consisted of debulking of residual tumor, placement of two tr
ansabdominal perfusion cannulae and administration of high-dose intraperito
neal chemotherapy at 40 degrees C using a simple, disposable perfusion circ
uit. Flow rates were maintained at 1 l/min, and inflow and outflow temperat
ures maintained at 42 and 40 degrees C, respectively. To date, three patien
ts have undergone both phases of the protocol, with no perioperative compli
cations related to either hyperthermia or end-organ toxicity. One patient d
ied of progressive disease after three months, and two patients are alive a
nd well. One patient developed a small bower anastomotic leak three weeks a
fter operation. In summary, intraoperative hyperthermic peritoneal chemothe
rapy may play a role in novel approaches to the treatment of peritoneal mal
ignancies previously unresponsive to traditional chemotherapeutic regimens.