Intra-arterial Cereport (RMP-7) and carboplatin: A dose escalation study for recurrent malignant gliomas

被引:45
作者
Cloughesy, TF
Black, KL
Gobin, YP
Farahani, K
Nelson, G
Villablanca, P
Kabbinavar, F
Vineula, F
Wortel, CH
机构
[1] Univ Calif Los Angeles, Dept Neurol, Sch Med, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Surg, Sch Med, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Dept Radiol, Sch Med, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Dept Med, Sch Med, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Sch Med, Los Angeles, CA 90024 USA
[6] Alkermes Inc, Cambridge, MA USA
关键词
blood-brain barrier; bradykinin; brain tumor; carboplatin; glioma; intra-arterial; RMP-7;
D O I
10.1097/00006123-199902000-00015
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: Animal and human studies have shown increased delivery of radiolabeled compounds across the blood-brain-tumor barrier using intra-arterial (IA) Cereport (RMP-7; Alkermes Inc., Cambridge, MA) with a radiolabeled tracer. This present study assesses the safety, tolerance, and preliminary efficacy of the IA administration of carboplatin with Cereport. METHODS: An open-label dose escalation study of IA Cereport (10-300 ng/kg) with 100 mg of IA carboplatin was conducted in 11 patients with recurrent malignant gliomas and 1 patient treated adjuvantly after radiation therapy. Tumor size and laboratory and clinical statuses were assessed. RESULTS: Adverse events were mainly neurological in nature and corresponded to the anatomic location of the tumor. Karnofsky performance scale scores did not decline, overall, for those patients who had tumor response. Tumor shrinkage was observed in three of six evaluable patients who received a dose of 300 ng/kg with durable responses of 60, 64, and 106+ weeks. CONCLUSION: Previous studies have demonstrated increased permeability in human gliomas using IA Cereport. This study demonstrates durable imaging responses using 100 mg of IA carboplatin in combination with Cereport, The drug combination in this patient population seems to be safe and acceptable, providing a novel means of antitumor dose intensification.
引用
收藏
页码:270 / 278
页数:9
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