Torka Pallawi, Al Ustwani Omar, Wetzler Meir, Wang Eunice S, Griffiths Elizabeth A
Leukemia Section, Department of Medicine, Roswell Park Cancer Institute,Elm and Carlton Streets, Buffalo, NY 14263, USA.
Leukemia Section, Department of Medicine, Roswell Park Cancer Institute,Elm and Carlton Streets, Buffalo, NY 14263, USA.
Blood Rev. 2016 May;30(3):201-11. doi: 10.1016/j.blre.2015.11.004. Epub 2015 Dec 3.
Parenteral arsenic trioxide (ATO) has been firmly established as a standard therapy for acute promyelocytic leukemia (APL). Despite widespread use of oral arsenicals in medicine historically, they had disappeared from modern pharmacopeia until oral ATO was redeveloped in Hong Kong in 2000. Since then, over 200 patients with leukemia (predominantly APL) have been treated with oral ATO in Hong Kong and China. Oral arsenic trioxide and other formulations of arsenic appear to have a clinical efficacy comparable to that of IV formulations. These drugs given orally also appear to have a slightly better safety profile, lower operational costs and improved convenience for patients. The clinical experience with oral ATO has previously been reported piecemeal as case series, pilot studies or subgroup analyses rather than in a comprehensive cohort. In this report we attempt to synthesize the published English language literature on oral arsenicals and present the argument for further development of these compounds. Systematic study of this drug with well-designed randomized multi-center clinical trials is needed to accelerate its development and incorporation into clinical practice.
胃肠外注射三氧化二砷(ATO)已被确认为急性早幼粒细胞白血病(APL)的标准疗法。尽管历史上口服砷剂在医学上被广泛使用,但它们已从现代药典中消失,直到2000年口服ATO在香港重新研发出来。从那时起,香港和中国已有200多名白血病患者(主要是APL)接受了口服ATO治疗。口服三氧化二砷和其他砷制剂似乎具有与静脉注射制剂相当的临床疗效。口服这些药物似乎安全性略好、运营成本更低且对患者更方便。此前口服ATO的临床经验只是作为病例系列、试点研究或亚组分析零星报道,而非综合队列研究。在本报告中,我们试图综合已发表的关于口服砷剂的英文文献,并提出进一步开发这些化合物的理由。需要通过精心设计的随机多中心临床试验对该药物进行系统研究,以加速其开发并将其纳入临床实践。