Honess D J, Bleehen N M
Br J Radiol. 1985 Jan;58(685):63-72. doi: 10.1259/0007-1285-58-685-63.
The magnitude of potentiation by whole body hyperthermia (45 min at 41 degrees C) of cis-platinum (DDP), CCNU, BCNU, chlorambucil and melphalan (Mel) on two tumours was compared with that on marrow in C3H mice. Drug damage was assayed in the KHT tumour by growth delay and in the RIF-1 tumour by clonogenic cell survival 24 h after treatment and/or by growth delay. Toxicity to marrow stem cells was assayed 24 h after treatment, by the spleen colony technique. When drug was given at the start of heating, all drugs were potentiated both in tumour and marrow to varying degrees. However, there was no therapeutic gain for the combined treatment with DDP on RIF-1, with CCNU or BCNU on KHT, or with CHL on either RIF-1 or KHT. Therapeutic ratios for Mel of 1.9 to 2.0 for KHT and of 1.1 to 1.8 in RIF-1 were measured over the dose range 7.5 to 15.0 mg/kg in unheated animals, indicating net therapeutic gain under these conditions. An absolute therapeutic gain was found for Mel in KHT when Mel was given 30 min before the start of heat.
比较了全身热疗(41℃下45分钟)对顺铂(DDP)、环己亚硝脲(CCNU)、卡氮芥(BCNU)、苯丁酸氮芥和美法仑(Mel)对C3H小鼠两种肿瘤的增效幅度与对骨髓的增效幅度。通过生长延迟测定KHT肿瘤中的药物损伤,通过治疗后24小时的克隆形成细胞存活率和/或生长延迟测定RIF-1肿瘤中的药物损伤。通过脾集落技术在治疗后24小时测定对骨髓干细胞的毒性。当在加热开始时给予药物时,所有药物在肿瘤和骨髓中均有不同程度的增效。然而,RIF-1肿瘤联合DDP治疗、KHT肿瘤联合CCNU或BCNU治疗,以及RIF-1或KHT肿瘤联合苯丁酸氮芥(CHL)治疗均未获得治疗益处。在未加热动物中,剂量范围为7.5至15.0mg/kg时,KHT肿瘤中美法仑的治疗比为1.9至2.0,RIF-1肿瘤中为1.1至1.8,表明在这些条件下有净治疗益处。当在加热开始前30分钟给予美法仑时,发现KHT肿瘤中美法仑有绝对的治疗益处。