Krossnes B K, Schem B C, Nygaard B, Dahl O, Mella O
Department of Oncology, Haukeland Hospital, University of Bergen, Norway.
J Neurooncol. 1996 Mar;27(3):205-14. doi: 10.1007/BF00165476.
The cerebral BT4An glioma model in BD IX rats was used to study the effect of hyperthermia given in combination with radiotherapy (thermoradiotherapy) in the treatment of brain tumours. A single treatment with high dose rate radiation was given to a local brain field. Local brain hyperthermia was given at 42.4 degrees C for 45 min by externally applied microwaves (700 MHz), immediately before radiotherapy (10 Gy). In a pilot study, thermoradiotherapy increased the median life span with 20 days compared to controls, which was significantly better than that observed after radiotherapy alone (7 days). In an extended experiment the corresponding figures for thermoradiotherapy, hyperthermia alone and radiotherapy alone were 12.5, 3.5, and 3.5 days, respectively. Thermoradiotherapy was significantly better than radiotherapy and hyperthermia alone. There was no acute mortality in these experiments. Neurological side-effects were infrequent, of slight degree and reversible. The present study shows that a survival benefit of adding hyperthermia to radiotherapy can be achieved without unacceptable neurological side-effects in an animal glioma model.
采用BD IX大鼠脑BT4An胶质瘤模型研究热疗联合放疗(热放疗)治疗脑肿瘤的效果。对局部脑区进行单次高剂量率放疗。在放疗(10 Gy)前,立即通过外部施加微波(700 MHz)在42.4℃进行局部脑热疗45分钟。在一项初步研究中,与对照组相比,热放疗使中位生存期延长了20天,这明显优于单独放疗后的观察结果(7天)。在一项扩展实验中,热放疗、单纯热疗和单纯放疗的相应数据分别为12.5天、3.5天和3.5天。热放疗明显优于单纯放疗和单纯热疗。这些实验中没有急性死亡情况。神经副作用很少见,程度轻微且可逆。本研究表明,在动物胶质瘤模型中,放疗联合热疗可实现生存获益,且不会产生不可接受的神经副作用。