Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, Division of Clinical Pharmacology and Toxicology, McMaster University, Hamilton, Ontario, Canada.
Clin Invest Med. 2024 Mar 1;47(1):13-22. doi: 10.3138/cim-2024-2569.
Immune thrombocytopenia (ITP) is an autoimmune disease characterized by low platelet counts and increased risk of bleeding. After corticosteroids with or without intravenous immune globulin (first-line treatment), second-line treatment options include rituximab, splenectomy, thrombopoietin receptor agonists (TPO-RAs), and fostamatinib. In Canada, the choice of second-line therapy is influenced by access to medications. The goals of this narrative review are to 1) summarize the evidence for the use of TPO-RAs and other second-line therapies in ITP and 2) highlight differences in public funding criteria for TPO-RAs across provinces and territories in Canada.
We conducted a literature review of second-line therapies for ITP. We solicited information on public funding programs for TPO-RAs in Canada from health care providers, pharmacists, and provincial ministries of health.
Head-to-head trials involving TPO-RAs, rituximab, splenectomy, and fostamatinib are lacking. There is substantial evidence of effect for TPO-RAs in improving platelet count levels, health-related quality of life, bleeding, and fatigue from placebo-controlled trials and observational studies; however, access to TPO-RAs through provincial funding programs in Canada is variable. Splenectomy failure is a prerequisite for the funding of TPO-RAs in Ontario, Manitoba, and Saskatchewan, but not in Alberta or Quebec. Other provinces either do not have access to public funding or funding is provided on a case-by-case basis.
TPO-RAs are effective second-line therapies for the treatment of ITP; however, access is variable across Canada, which results in health disparities and poor uptake of international treatment guidelines.
免疫性血小板减少症(ITP)是一种自身免疫性疾病,其特征为血小板计数降低,出血风险增加。在使用皮质类固醇联合或不联合静脉注射免疫球蛋白(一线治疗)后,二线治疗选择包括利妥昔单抗、脾切除术、血小板生成素受体激动剂(TPO-RAs)和 fostamatinib。在加拿大,二线治疗的选择受到药物获取途径的影响。本文综述的目的是:1)总结 TPO-RAs 和其他 ITP 二线治疗的证据;2)突出加拿大各省和地区 TPO-RAs 公共资助标准的差异。
我们对 ITP 的二线治疗进行了文献回顾。我们向医疗保健提供者、药剂师和各省卫生部征求了有关加拿大 TPO-RAs 公共资助计划的信息。
缺乏涉及 TPO-RAs、利妥昔单抗、脾切除术和 fostamatinib 的头对头试验。来自安慰剂对照试验和观察性研究的大量证据表明 TPO-RAs 可有效提高血小板计数水平、改善健康相关生活质量、减少出血和疲劳;然而,加拿大各省通过省级资助计划获得 TPO-RAs 的途径存在差异。在安大略省、曼尼托巴省和萨斯喀彻温省,TPO-RAs 的资助前提是脾切除术失败,但在艾伯塔省和魁北克省则不是。其他省份要么无法获得公共资金,要么根据具体情况提供资金。
TPO-RAs 是治疗 ITP 的有效二线治疗方法;然而,加拿大各地的准入情况存在差异,导致了健康差距和国际治疗指南的接受度不佳。