Gill Harinder, Wong Raymond S M, Kwong Yok-Lam
Department of Medicine, Queen Mary Hospital, Hong Kong, China.
Sir Y.K. Pao Centre for Cancer and Department of Medicine and Therapeutics, Prince of Wales Hospital, the Chinese University of Hong Kong, Hong Kong, China.
Ther Adv Hematol. 2017 May;8(5):159-174. doi: 10.1177/2040620717693573. Epub 2017 Feb 1.
Thrombopoietin (TPO) is the most potent cytokine stimulating thrombopoiesis. Therapy with exogenous TPO is limited by the formation of antibodies cross-reacting with endogenous TPO. Mimetics of TPO are compounds with no antigenic similarity to TPO. Eltrombopag is an orally-active nonpeptide small molecule that binds to the transmembrane portion of the TPO receptor MPL. Initial trials of eltrombopag have centered on immune thrombocytopenia (ITP), which is due to both increased destruction and decreased production of platelets. Eltrombopag at 25-75 mg/day has been shown to be highly effective in raising the platelet count in ITP with suboptimal response to immunosuppression and splenectomy. These successful results led to the exploration of eltrombopag in other thrombocytopenic disorders. In hepatitis C viral infection, eltrombopag raises the platelet count sufficiently enough to allow treatment with ribavirin and pegylated interferon. Because MPL is expressed on hematopoietic cells, eltrombopag use in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) might enhance leukemic proliferation. Clinical trials of eltrombopag in MDS and AML, however, have shown amelioration of thrombocytopenia without promoting disease progression. In severe aplastic anemia (SAA) not responding to immunosuppression with anti-thymocyte globulin (ATG) and cyclosporine, eltrombopag as a single agent at 150-300 mg/day results in an overall response rate of 40-70%. At high doses, adverse effects including pigmentation, gastrointestinal upset and hepatic derangement have become evident. Current studies have examined the first-line use of eltrombopag in combination with ATG in SAA. In a recent study, eltrombopag used at 150 mg/day with horse ATG resulted in an overall response rate of 90% in newly diagnosed SAA patients, with a complete response rate of about 50%. Clonal karyotypic aberrations are, however, found in 10-20% of SAA patients treated with eltrombopag. The safety and efficacy of eltrombopag in SAA require further evaluation, particularly when it is used with less intensive immunosuppression.
血小板生成素(TPO)是刺激血小板生成的最有效细胞因子。外源性TPO治疗受到与内源性TPO发生交叉反应的抗体形成的限制。TPO模拟物是与TPO无抗原相似性的化合物。艾曲泊帕是一种口服活性非肽小分子,可与TPO受体MPL的跨膜部分结合。艾曲泊帕的初步试验主要集中在免疫性血小板减少症(ITP),该病是由于血小板破坏增加和生成减少所致。每天25 - 75毫克的艾曲泊帕已被证明在提高对免疫抑制和脾切除术反应欠佳的ITP患者的血小板计数方面非常有效。这些成功结果促使人们探索艾曲泊帕在其他血小板减少性疾病中的应用。在丙型肝炎病毒感染中,艾曲泊帕能充分提高血小板计数,从而使患者能够接受利巴韦林和聚乙二醇干扰素治疗。由于MPL在造血细胞上表达,在骨髓增生异常综合征(MDS)和急性髓系白血病(AML)中使用艾曲泊帕可能会增强白血病细胞的增殖。然而,艾曲泊帕在MDS和AML中的临床试验表明,其可改善血小板减少症,且不会促进疾病进展。在对抗胸腺细胞球蛋白(ATG)和环孢素免疫抑制无反应的重型再生障碍性贫血(SAA)中,每天150 - 300毫克的艾曲泊帕单药治疗的总缓解率为40 - 70%。在高剂量时,包括色素沉着、胃肠道不适和肝脏紊乱在内的不良反应已变得明显。目前的研究已考察了艾曲泊帕与ATG联合用于SAA一线治疗的情况。在最近一项研究中,每天150毫克的艾曲泊帕与马ATG联合使用,使新诊断的SAA患者的总缓解率达到90%,完全缓解率约为50%。然而,在接受艾曲泊帕治疗的SAA患者中,10 - 20%的患者发现有克隆性核型异常。艾曲泊帕在SAA中的安全性和有效性需要进一步评估,尤其是在与强度较低的免疫抑制联合使用时。