## Abstract Cisplatin (CDDP) administration by the intraβarterial hepatic route (i.a.h.) in patients with primary or metastatic liver malignancies could enhance the antiβtumor activity of the drug and reduce its systemic toxicity. The aim of the present study was to compare Pt pharmacokinetics and
Intra-arterial cisplatin for the treatment of malignant gliomas
β Scribed by Herbert B. Newton; Michaelyn A. Page; Larry Junck; Harry S. Greenberg
- Publisher
- Springer US
- Year
- 1989
- Tongue
- English
- Weight
- 571 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0167-594X
No coin nor oath required. For personal study only.
β¦ Synopsis
Cisplatin (DDP) is a chemotherapeutic agent that has shown efficacy against primary CNS malignancies. Intraarterial (IA) administration of DDP to patients with brain tumors should produce higher peak levels of drug than intravenous (IV) administration of an identical dose and reduce systemic toxicity. Twelve patients with malignant glioma were entered into the study. All had failed irradiation, 11 had failed IA BCNU. Each patient received IA DDP, 58-100 mg/m 2, into the internal carotid artery at four to six week intervals. One of 12 patients had a partial response of 6 months. The remaining 11 patients had progressive disease [10] or severe complications [1]. Toxicity included seizures in four patients, weakness and/or aphasia in four patients, coma in two patients, and visual deterioration in two patients. IA DDP has very limited efficacy in patients with malignant gliomas after failure of nitrosoureas and is associated with an unacceptable level of toxicity. IA DDP may be more effective when used as initial chemotherapy of malignant gliomas.
π SIMILAR VOLUMES
Twenty-one patients with recurrent malignant glioma who had failed prior chemotherapy with nitrosoureas were treated with high-dose intravenous cisplatin on days 1 and 8 of successive 4 week cycles. Fourteen patients were evaluable for response. Four patients showed partial responses; mean time to t