Schrezenmeier Hubert, Körper Sixten, Höchsmann Britta
Institute of Transfusion Medicine, University of Ulm, Ulm, Germany.
Expert Rev Hematol. 2015 Feb;8(1):89-99. doi: 10.1586/17474086.2015.978759.
Aplastic anemia is a rare life-threatening bone marrow failure that is characterized by bicytopenia or pancytopenia in the peripheral blood and a hypoplastic or aplastic bone marrow. The patients are at risk of infection and hemorrhage due to neutropenia and thrombocytopenia and suffer from symptoms of anemia. The main treatment approaches are allogeneic stem cell transplantation and immunosuppression. Here, we review current standard immunosuppression and the attempts that have been made in the past two decades to improve results: review of recent developments also reveals that sometimes not only the advent of new drugs, good ideas and well-designed clinical trials decide the progress in the field but also marketing considerations of pharmaceutical companies. Aplastic anemia experts unfortunately had to face the situation that efficient drugs were withdrawn simply for marketing considerations. We will discuss the current options and challenges in first-line treatment and management of relapsing and refractory patients with an emphasis on adult patients. Some promising new approaches are currently under investigation in prospective, randomized trials.
再生障碍性贫血是一种罕见的危及生命的骨髓衰竭疾病,其特征为外周血全血细胞减少或两系血细胞减少以及骨髓增生低下或再生障碍。由于中性粒细胞减少和血小板减少,患者有感染和出血风险,并伴有贫血症状。主要治疗方法是异基因干细胞移植和免疫抑制。在此,我们回顾当前的标准免疫抑制方法以及过去二十年来为改善治疗效果所做的尝试:对近期进展的回顾还表明,有时不仅新药的出现、好的想法和精心设计的临床试验决定了该领域的进展,制药公司的市场考量也起到了作用。不幸的是,再生障碍性贫血专家不得不面对高效药物仅仅因为市场考量而被撤市的情况。我们将讨论一线治疗以及复发和难治性患者管理中的当前选择和挑战,重点关注成年患者。目前一些有前景的新方法正在前瞻性随机试验中进行研究。