Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada; Department of Medicine and Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada; Canadian Blood Services, Hamilton, Ontario, Canada.
Transfusion. 2013 Nov;53(11):2807-12. doi: 10.1111/trf.12139. Epub 2013 Mar 3.
Thrombopoietin receptor agonists (TRAs) are effective treatments for immune thrombocytopenia (ITP). However, continuous therapy is generally required to maintain platelet (PLT) count responses.
In this case series, we describe ITP patients from our practice who achieved durable responses to the TRAs romiplostim and eltrombopag. Patients were classified as having a definite TRA-induced remission if PLT counts increased above 100 × 10(9) /L after TRA treatment and remained above 100 × 10(9) /L even after the medication was discontinued; or a possible TRA-induced remission if PLT counts increased above 100 × 10(9) /L, remained elevated for at least 3 months after the medication was discontinued, but a subsequent relapse occurred or the effect of other disease-modifying therapies could not be excluded.
Of 31 patients with chronic ITP treated with TRAs in our practice, nine patients achieved a PLT count response with either romiplostim (n = 6) or eltrombopag (n = 3) that was maintained even after the medications were discontinued. Three patients met criteria for a definite TRA-induced remission, each after exposure to romiplostim. Patients had ITP for a median of 7.8 years and had failed a median of four prior therapies including eight patients who had a splenectomy. We documented a progressive decline in anti-glycoprotein IIbIIIa PLT autoantibodies in one patient while on treatment.
Some patients with ITP can achieve sustained PLT count responses after the use of TRAs. This observation raises the possibility that these agents may restore immune tolerance to PLT antigens in some patients and supports the practice of down titrating the dose.
血小板生成素受体激动剂(TRAs)是治疗免疫性血小板减少症(ITP)的有效方法。然而,通常需要持续治疗来维持血小板(PLT)计数的反应。
在本病例系列中,我们描述了来自我们实践的 ITP 患者,他们对 TRA 罗米司亭和艾曲波帕有持久的反应。如果 PLT 计数在 TRA 治疗后增加到 100×10(9)/L 以上,并且即使在停止用药后仍保持在 100×10(9)/L 以上,则将患者归类为具有明确的 TRA 诱导缓解;或者,如果 PLT 计数增加到 100×10(9)/L 以上,在停止用药后至少 3 个月仍保持升高,但随后发生复发或不能排除其他疾病修正治疗的效果,则归类为可能的 TRA 诱导缓解。
在我们的实践中,用 TRAs 治疗的 31 例慢性 ITP 患者中,有 9 例患者的 PLT 计数反应得到了罗米司亭(n=6)或艾曲波帕(n=3)的治疗,即使在停止用药后也得到了维持。3 例患者符合明确的 TRA 诱导缓解标准,均在暴露于罗米司亭后符合。患者的 ITP 病史中位数为 7.8 年,中位数经历了 4 次既往治疗失败,包括 8 例脾切除术患者。我们在一名患者接受治疗时记录到抗糖蛋白 IIbIIIa PLT 自身抗体的逐渐下降。
一些 ITP 患者在使用 TRA 后可以获得持续的 PLT 计数反应。这一观察结果提出了这样一种可能性,即这些药物可能在某些患者中恢复对 PLT 抗原的免疫耐受,并支持逐渐减少剂量的做法。