Foo S H, Choi I S, Berenstein A, Wise A, Ransohoff J, Koslow M, George A, Lin J, Feigin I, Budzilovich G
Neurology. 1986 Nov;36(11):1437-44. doi: 10.1212/wnl.36.11.1437.
We treated five patients with 11 supraophthalmic infusions of BCNU at 200 mg/m2 every 2 months. All three patients with residual tumors showed marked CT response after one infusion. Two patients with bilateral tumors had no response on the contralateral side. All four evaluable cases showed evidence of BCNU neurotoxicity. CT findings superficially resembled tumor recurrence, but white matter changes, nonspecific gyral enhancement, and delayed calcification were more indicative of neurotoxicity. There were no procedure-related complications. One autopsy suggested that direct parenchymal damage might be responsible for delayed neurotoxicity. Supraophthalmic BCNU infusion, at this dosage, is too toxic for cerebral tissue.
我们每2个月以200mg/m²的剂量对5例患者进行了11次超眼动脉输注卡莫司汀(BCNU)治疗。所有3例有残留肿瘤的患者在一次输注后CT显示有明显反应。2例双侧肿瘤患者的对侧无反应。所有4例可评估病例均显示有BCNU神经毒性的证据。CT表现表面上类似肿瘤复发,但白质改变、非特异性脑回强化和延迟钙化更提示神经毒性。未出现与操作相关的并发症。一次尸检提示,实质直接损伤可能是延迟性神经毒性的原因。以这种剂量进行超眼动脉BCNU输注对脑组织毒性过大。