Cloughesy T F, Gobin Y P, Black K L, Viñuela F, Taft F, Kadkhoda B, Kabbinavar F
Jonsson Comprehensive Cancer Center, Department of Neurology, UCLA School of Medicine, USA.
J Neurooncol. 1997 Nov;35(2):121-31. doi: 10.1023/a:1005856002264.
To perform in intra-arterial dose escalation study of carboplatin based on hemispheric blood-flow estimation in patients with recurrent malignant glioma. The primary purpose was to determine the maximally tolerated intra-arterial dose.
Methods included: 1) selective intra-arterial delivery performed with modern microcatheters, 2) pulsatile infusion, and 3) dosage based on local cerebral blood-flow estimation (middle cerebral artery 60%, anterior cerebral artery 20%, posterior cerebral artery 15%, and anterior choroidal artery 5% of the hemispheric blood-flow). The deliveries were performed above the ophthalmic artery in the anterior circulation, or above the anterior inferior cerebellar arteries in the posterior circulation. The doses were escalated from 200 mg/hemisphere at 50 mg increments. Twenty-one patients were studied (14 with glioblastoma multiforme, five anaplastic astrocytoma, one aggressive low-grade glioma, one metastasis). Patients had recurrent glioma limited to one hemisphere and Karnofsky score of 50 or greater. Concomitant therapies were allowed.
Carboplatin was escalated to a dose of 1400 mg/hemisphere. One patient had a permanent neuromotor decline. The predominant toxicity was hematopoietic. The median time to tumor progression was 22 weeks, median survival 39 weeks, and the response rate 70% (50% SD and 20% PR) of 19 patients.
Hemispheric blood-flow estimation allowed us to escalate the dose of intra-arterial carboplatin to twice what was previously considered safe. Responses compared favorably to previous studies. Further studies are needed to determine if this method will provide improved and durable responses.
基于复发性恶性胶质瘤患者的半球血流量估计,进行卡铂的动脉内剂量递增研究。主要目的是确定最大耐受动脉内剂量。
方法包括:1)使用现代微导管进行选择性动脉内给药;2)脉冲式输注;3)基于局部脑血流量估计给药(大脑中动脉占半球血流量的60%,大脑前动脉占20%,大脑后动脉占15%,脉络膜前动脉占5%)。给药在前循环中于眼动脉上方进行,或在后循环中于小脑前下动脉上方进行。剂量以50mg的增量从200mg/半球开始递增。共研究了21例患者(14例多形性胶质母细胞瘤,5例间变性星形细胞瘤,1例侵袭性低级别胶质瘤,1例转移瘤)。患者复发性胶质瘤局限于一个半球,卡氏评分50分或更高。允许同时进行其他治疗。
卡铂剂量递增至1400mg/半球。1例患者出现永久性神经运动功能减退。主要毒性为血液学毒性。19例患者的肿瘤进展中位时间为22周,中位生存期为39周,缓解率为70%(50%为疾病稳定,20%为部分缓解)。
半球血流量估计使我们能够将动脉内卡铂剂量递增至之前认为安全剂量的两倍。与以往研究相比,疗效良好。需要进一步研究以确定该方法是否能提供更好且持久的疗效。