Onoyama Y
Gan No Rinsho. 1983 May;29(6):718-25.
Misonidazole is the first hypoxic cell sensitizer which is introduced into the world-wide clinical trials. More than 500 patients have been treated with misonidazole in Japan. Phase I study, involved 106 patients, established its pharmacology, toxicities and safe dose regimens to Japanese. Total amount of 10.0g/m2, 1.5g/m2 once, 1.0g/m2 twice and 0.5g/m2 5 times a week, can be administered with acceptable toxicities and give plasma levels of the sensitizer enough to expect sensitizing effect to a certain degree. Several preliminary studies demonstrated the effect of the drug by factor about 1.3 in tumor regression, however the results of most Phase II studies were controversial. Final determination of its efficacy should be postponed until the completion of randomized Phase III studies with large number of patients, which are ongoing in the United States, Japan and so on. Considering the neurotoxicity of misonidazole, it is not the ideal sensitizer, but should be regarded as the first generation drug for hypoxic cells. Since a number of less toxic sensitizers are under development at present, more effective and safe drugs will appear in the near future.
米索硝唑是第一种被引入全球临床试验的乏氧细胞增敏剂。在日本,已有500多名患者接受了米索硝唑治疗。一项涉及106名患者的I期研究确定了其对日本人的药理学、毒性和安全剂量方案。总剂量为10.0g/m²,可单次给予1.5g/m²、分两次给予1.0g/m²或每周5次给予0.5g/m²,这些给药方式的毒性均可接受,且能使增敏剂的血浆水平达到足以在一定程度上预期增敏效果。几项初步研究表明,该药物在肿瘤消退方面有大约1.3倍的效果,然而大多数II期研究的结果存在争议。其疗效的最终确定应推迟到美国、日本等正在进行的大量患者参与的随机III期研究完成之后。考虑到米索硝唑的神经毒性,它并非理想的增敏剂,但应被视为第一代乏氧细胞药物。由于目前有多种毒性较小的增敏剂正在研发中,在不久的将来将会出现更有效、更安全的药物。