Thalassemia Center, Burjeel Medical City, Abu Dhabi, United Arab Emirates.
International Network of Hematology, London, UK.
Am J Hematol. 2021 Nov 1;96(11):1518-1531. doi: 10.1002/ajh.26316. Epub 2021 Aug 18.
The treatment landscape for patients with β-thalassemia is witnessing a swift evolution, yet several unmet needs continue to persist. Patients with transfusion-dependent β-thalassemia (TDT) primarily rely on regular transfusion and iron chelation therapy, which can be associated with considerable treatment burden and cost. Patients with non-transfusion-dependent β-thalassemia (NTDT) are also at risk of significant morbidity due to the underlying anemia and iron overload, but treatment options in this patient subgroup are limited. In this review, we provide updates on clinical trials of novel therapies targeting the underlying pathology in β-thalassemia, including the α/non-α-globin chain imbalance, ineffective erythropoiesis, and iron dysregulation.
β-地中海贫血患者的治疗现状正在迅速发展,但仍存在一些未满足的需求。依赖输血的β-地中海贫血(TDT)患者主要依赖于定期输血和铁螯合治疗,但这可能会带来相当大的治疗负担和成本。非输血依赖的β-地中海贫血(NTDT)患者也存在严重发病的风险,这是由于基础贫血和铁过载所致,但该患者亚组的治疗选择有限。在这篇综述中,我们提供了针对β-地中海贫血基础病理的新型治疗临床试验的最新进展,包括α/非α-球蛋白链失衡、无效红细胞生成和铁失调。