SELECTIVE INTRAARTERIAL CHEMOTHERAPY WITH A COMBINATION OF ETOPOSIDE AND CISPLATIN FOR MALIGNANT GLIOMAS - PRELIMINARY-REPORT

We administered selective intra-arterial chemotherapy consisting of a combination of etoposide and cisplatin to 20 patients with malignant g lioma (seven with recurrent and six with enlarged tumors after initial treatment, and seven newly diagnosed patients). Evaluation of efficac y was based on computed tomographic and magnetic resonance imaging fin dings. In the process of establishing a safe technique for superselect ive intra-arterial chemotherapy, we encountered cerebrovascular accide nts in two patients (after etoposide in one and after etoposide plus c isplatin in the other). In these two cases, 100 mg/m2 of etoposide and 100 mg/m2 of cisplatin were delivered via the horizontal segment of t he middle cerebral artery (M1) or the tip of the basilar artery, with the infusion time reduced to 20 minutes. Thereafter, the etoposide was diluted, and the doses of both drugs were reduced to 80 or 50 mg/m2, and finally to 60 mg/m2, and both were infused over 60 minutes. In add ition, for prevention of local spasm, papaverine hydrochloride and nic ardipine were given via the same catheter at 5-minute intervals during administration of etoposide and cisplatin. No complications developed in the later cases. Thereafter, selective intra-arterial infusion of etoposide and cisplatin into the anterior cerebral artery, middle cere bral artery, posterior cerebral artery, or the basilar artery for mali gnant gliomas in the basal ganglia, internal capsule, and brainstem-a procedure generally considered risky in terms of potential complicatio ns-was performed safely, with tolerable side effects. Computed tomogra phy and magnetic resonance imaging indicated improvement in 13 patient s, including four whose tumors completely disappeared. This method of intraarterial chemotherapy may be useful as an adjuvant treatment for malignant glioma.