Postgraduate Research Institute of Science, Technology, Environment and Medicine, 3, Ammochostou Street, Limassol 3021, Cyprus.
Expert Opin Drug Saf. 2010 Jul;9(4):633-41. doi: 10.1517/14740338.2010.497138.
Thousands of iron loaded patients are using deferasirox, who are not aware of the new, fatal and irreversible serious toxic side effects, the need for prophylaxis and the availability of more effective and less toxic chelation therapies.
Updating on efficacy issues in relation to the introduction of higher deferasirox doses and comparison to existing chelation therapies. A new maximum dose of 40 mg/kg/day has been introduced for deferasirox in an attempt to achieve negative iron balance in thalassemia and other transfused iron loaded patients. A marginal increase in cardiac iron removal using doses of 30 - 40 mg/kg/day suggests that the rate of iron removal by deferasirox is insufficient by comparison to the deferiprone/deferoxamine combination, where total and rapid clearance of excess cardiac iron and normalization of the body iron stores could be achieved.
Identification of drug interactions and new fatal and permanent toxic side effects of deferasirox and implications on efficacy, toxicity and cost of using higher doses. Deferasirox has been identified to cause fatal gastrointestinal hemorrhages, renal tubulopathy, hepatic and renal failure, alopecia and anaphylactic reactions in addition to previously reported fatal or serious toxic side effects such as agranulocytosis, renal and hepatic toxicity, skin rash and gastric intolerance. Interactions with UDP-glucuronosyl transferase inducers, CYP2C8 and CYP3A4 substrates and drugs affecting enterohepatic recycling are likely to affect deferasirox's efficacy and toxicity. Increased toxicity is expected from the use of higher doses of deferasirox and regular prophylactic monitoring is required to avoid fatal and permanent toxicity incidences. The increased costs from higher doses of deferasirox will mostly affect patients living in the developing countries.
Only few patients may benefit from the introduction of higher doses of deferasirox. There is a need for introducing more effective prophylactic measures. Safer, more effective and less costly chelation treatments are available using deferiprone, deferoxamine and their combination.
成千上万的铁负荷患者正在使用地拉罗司,他们不知道新的、致命的和不可逆转的严重毒性副作用,需要预防措施以及更有效和毒性更小的螯合疗法。
更新与更高剂量地拉罗司引入相关的疗效问题,并与现有的螯合疗法进行比较。地拉罗司的新最大剂量已提高到 40mg/kg/天,试图在铁过载患者中实现铁负平衡。使用 30-40mg/kg/天的剂量,心脏铁清除量略有增加,表明与地拉罗司/去铁酮/去铁胺联合用药相比,地拉罗司的铁清除率不足,后者可迅速清除多余的心脏铁并使体内铁储存正常化。
确定地拉罗司的药物相互作用和新的致命和永久性毒性副作用及其对使用更高剂量的疗效、毒性和成本的影响。除了先前报道的致命或严重毒性副作用,如粒细胞缺乏症、肾肝毒性、皮疹和胃不耐受外,地拉罗司已被确定会导致致命的胃肠道出血、肾小管病、肝肾功能衰竭、脱发和过敏反应。与 UDP-葡糖醛酸基转移酶诱导剂、CYP2C8 和 CYP3A4 底物以及影响肠肝循环的药物相互作用可能会影响地拉罗司的疗效和毒性。使用更高剂量的地拉罗司会增加毒性,需要定期进行预防性监测以避免致命和永久性毒性事件的发生。更高剂量的地拉罗司增加的成本将主要影响发展中国家的患者。
只有少数患者可能受益于地拉罗司更高剂量的引入。需要引入更有效的预防措施。使用去铁酮、去铁胺及其联合用药,可提供更安全、更有效和更廉价的螯合治疗。