Department of Hematology and Oncology, Nagoya Daini Red Cross Hospital, Showa-ku, Nagoya, Japan.
J Clin Pharm Ther. 2012 Dec;37(6):729-32. doi: 10.1111/j.1365-2710.2012.01353.x. Epub 2012 May 14.
Although new thrombopoietin (TPO) receptor agonist drugs, such as romiplostim and eltrombopag, are highly effective and well tolerated for patients with immune thrombocytopenia (ITP) refractory to first-line treatments such as prednisolone, the cross-resistance of these two TPO receptor agonists is still unknown.
An 84-year-old Japanese female patient with steroid-refractory ITP received eltrombopag with a gradually increasing dose schedule from 12.5 to 25 mg/day, 37.5 mg/day and finally 50 mg/day. As no increase in platelet count was observed even at the maximum dose of 50 mg/day, and eltrombopag-related grade 3 elevation of aspartate aminotransferase was observed, another TPO receptor agonist, romiplostim, was administered at 1 μg/kg/week subcutaneously. A rapid increase in platelet count was observed 1 week after the first injection. The dose of romiplostim was escalated to 4 μg/kg according to the platelet count and a complete response was achieved 7 weeks after the first injection without any adverse events.
The successful treatment of ITP refractory to eltrombopag with romiplostim strongly suggests that the absence of cross-resistance between these two approved TPO receptor agonists and possible differences in mechanism of action. Further study of the mechanisms of action of TPO receptor agonists is called for along with further exploration of the potential of romiplostim in refractory ITP.
虽然新型促血小板生成素(TPO)受体激动剂药物,如罗米司亭和艾曲波帕,对于对一线治疗(如泼尼松)耐药的免疫性血小板减少症(ITP)患者非常有效且耐受良好,但这两种 TPO 受体激动剂之间的交叉耐药性仍不清楚。
一位 84 岁的日本女性患者患有激素耐药性 ITP,接受艾曲波帕治疗,剂量逐渐增加,从每天 12.5 毫克增加到 25 毫克、37.5 毫克,最后增加到 50 毫克。由于即使在最大剂量 50 毫克/天时血小板计数也没有增加,并且观察到与艾曲波帕相关的 3 级天门冬氨酸氨基转移酶升高,因此给予另一种 TPO 受体激动剂罗米司亭,每周皮下注射 1μg/kg。首次注射后 1 周观察到血小板计数迅速增加。根据血小板计数将罗米司亭剂量递增至 4μg/kg,首次注射后 7 周达到完全缓解,无任何不良反应。
对艾曲波帕耐药的 ITP 用罗米司亭成功治疗强烈表明这两种已批准的 TPO 受体激动剂之间不存在交叉耐药性,并且可能存在作用机制的差异。需要进一步研究 TPO 受体激动剂的作用机制,并进一步探索罗米司亭在难治性 ITP 中的潜力。