Yoshida J, Wakabayashi T, Mizuno M, Sugita K, Yoshida T, Hori S, Mori T, Sato T, Karashima A, Kurisu K
Department of Neurosurgery, Nagoya University, Japan.
J Neurosurg. 1992 Jul;77(1):78-83. doi: 10.3171/jns.1992.77.1.0078.
Recombinant human tumor necrosis factor-alpha was administered intra-arterially to treat 20 cases of malignant gliomas, mostly progressive or recurrent. The optimum dosage was determined to be 1 x 10(5) U/sq m/day. Among the 10 evaluable patients treated at this dosage, two responded (one completely and one partially), resulting in a 20% response rate. Side effects were mild and easily controllable. Improvement of neurological symptoms was noted in 47% of the patients a few days after treatment, even when computerized tomography showed no tumor regression. This might have been due to the pleiotypic biological activity of tumor necrosis factor-alpha. Neuroradiographic observations revealed narrowing of the tumor-feeding artery, a decrease in tumor staining ability, and necrosis in the central part of a tumor. The authors suggest that intra-arterial administration of tumor necrosis factor-alpha may be an effective treatment for malignant glioma, including recurrent cases.
重组人肿瘤坏死因子-α经动脉内给药治疗20例恶性胶质瘤患者,大多为进展期或复发期患者。确定最佳剂量为1×10(5)U/平方米/天。在此剂量下接受治疗的10例可评估患者中,2例有反应(1例完全缓解,1例部分缓解),有效率为20%。副作用轻微且易于控制。47%的患者在治疗几天后神经症状有所改善,即使计算机断层扫描显示肿瘤无缩小。这可能归因于肿瘤坏死因子-α的多效性生物学活性。神经影像学观察显示肿瘤供血动脉变窄、肿瘤染色能力下降以及肿瘤中央部分坏死。作者认为,经动脉内给予肿瘤坏死因子-α可能是治疗恶性胶质瘤(包括复发病例)的一种有效方法。