首页> 外文期刊>International journal of hyperthermia: The official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group >Fever-range whole body thermotherapy combined with oxaliplatin: A curative regimen in a pre-clinical breast cancer model
【24h】

Fever-range whole body thermotherapy combined with oxaliplatin: A curative regimen in a pre-clinical breast cancer model

机译:发烧全身热疗法联合奥沙利铂:临床前乳腺癌模型的治疗方案

获取原文
       

摘要

Purpose: Studies were conducted to test whether fever-range whole body thermal therapy would boost the efficacy of oxaliplatin chemotherapy without substantial toxicity. Materials and methods: The effect of mild heat (40°C) on oxaliplatin cytotoxicity, cellular uptake, and platinum-DNA adduct formation was studied in vitro using the MTLn3 tumour cell line. In vivo oxaliplatin was administered at various doses and times before, during and after fever-range thermal therapy (6 h at 40°C) to rats bearing an MTLn3 mammary adenocarcinoma. Tumour growth, survival, and toxicity were measured to determine treatment outcome. Results: Heating halved the oxaliplatin IC-50 dose for MTLn3 cells. Cellular uptake of platinum and platinum adducts increased by 34% and 36%, respectively, with heat. In vivo, 50% of all rats given 10 mg/kg oxaliplatin 24 h before thermal therapy were completely immunologically cured, while a further 11% regressed their primary tumour but ultimately succumbed to metastases, and 17% experienced a limited response with increased survival. The curative response occurred only in a narrow range of doses, with most cures at 10 mg/kg. Thermochemotherapy-treated, but uncured, animals had delayed incidence and slowed growth of metastases. Anti-tumour efficacy was greatest, and toxicity was least, when oxaliplatin was administered 12 or 24 h before fever-range whole body thermal therapy. Conclusions: When properly dosed and scheduled, oxaliplatin thermochemotherapy achieved permanent eradication of all primary and metastatic tumours in 50% of animals, seemingly through an immune response. Successful clinical translation of this protocol would yield hitherto unseen cures and substantial improvement in quality of life.
机译:目的:进行研究以测试发烧范围的全身热疗是否可以提高奥沙利铂化疗的疗效,而不会产生实质性毒性。材料和方法:使用MTLn3肿瘤细胞系体外研究了温热(40°C)对奥沙利铂的细胞毒性,细胞摄取和铂-DNA加合物形成的影响。在发烧范围热疗法(在40°C下6 h)之前,期间和之后,以各种剂量和时间对体内Moxn3乳腺腺癌大鼠给药奥沙利铂。测量肿瘤的生长,存活率和毒性以确定治疗结果。结果:加热将MTLn3细胞的奥沙利铂IC-50剂量减半。加热时,细胞对铂和铂加合物的吸收分别增加了34%和36%。在体内,在热疗前24小时给予10 mg / kg奥沙利铂的所有大鼠中,有50%完全免疫治愈,而另外11%的大鼠使原发性肿瘤消退,但最终因转移而转移,而17%的人则表现出有限的反应并提高了生存率。治愈反应仅在很窄的剂量范围内发生,大多数治愈方法为10 mg / kg。经热化学疗法治疗但未治愈的动物延迟了发病率并减慢了转移的生长。当在发热范围的全身热疗前12或24 h服用奥沙利铂时,抗肿瘤功效最大,毒性最小。结论:按适当的剂量和日程安排,奥沙利铂热化学疗法似乎可以通过免疫反应永久消灭50%动物的所有原发性和转移性肿瘤。该方案的成功临床翻译将产生迄今为止看不见的治愈方法,并大大改善生活质量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号