Passweg Jakob R, Baldomero Helen, Basak Grzegorz W, Chabannon Christian, Corbacioglu Selim, Duarte Rafael, Kuball Jürgen, Lankester Arjan, Montoto Silvia, de Latour Régis Peffault, Snowden John A, Styczynski Jan, Yakoub-Agha Ibrahim, Arat Mutlu, Mohty Mohamad, Kröger Nicolaus
EBMT Activity Survey Office, Hematology, Department of Medicine, University Hospital, Basel, Switzerland.
Department of Hematology, Oncology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.
Bone Marrow Transplant. 2019 Oct;54(10):1575-1585. doi: 10.1038/s41409-019-0465-9. Epub 2019 Feb 6.
Hematopoietic cell transplantation (HCT) is widely used for acquired and congenital disorders of the hematopoietic system. Number of transplants done in Europe and associated countries continues to rise with 45,418 HCT in 41,100 patients [(17,155 allogeneic (42%) and 23,945 autologous (58%)] reported by 683 centers in 50 countries in 2017. Main indications were myeloid malignancies 10,147 (25%; 96% allogeneic), lymphoid malignancies 26,488 (64%; 19% allogeneic), solid tumors 1,607 (3.9%; 2% allogeneic), and nonmalignant disorders 2,667 (7%; 81% allogeneic). Trends in donor choice seen before continue, with growing numbers of haploidentical HCT and decreasing use of cord blood. Of interest is that after many years of continued growth, the number of patients receiving an allogeneic HCT for marrow failure is decreasing slightly (p < 0.001). Such a change may be explained by the use of thrombopoietin analogs in aplastic anemia patients. Other nonmalignant indications, however continue to grow, most importantly HCT for hemoglobinopathies by 36%, equally for thalassemias and sickle cell disease. Non-HCT cell therapies have increased by 28% since 2015 and genetically modified T cells is type of cell therapy with the fastest growth. These annual reports reflect current activity and trends and are useful for health-care planning.
造血细胞移植(HCT)广泛应用于造血系统的后天性和先天性疾病。欧洲及相关国家的移植数量持续上升,2017年50个国家的683个中心报告了41100例患者接受了45418次HCT(其中17155例为异基因移植(42%),23945例为自体移植(58%))。主要适应证为髓系恶性肿瘤10147例(25%;96%为异基因移植)、淋巴系恶性肿瘤26488例(64%;19%为异基因移植)、实体瘤1607例(3.9%;2%为异基因移植)和非恶性疾病2667例(7%;81%为异基因移植)。之前出现的供体选择趋势仍在继续,单倍体相合HCT数量不断增加,脐带血的使用减少。值得关注的是,在持续增长多年后,因骨髓衰竭接受异基因HCT的患者数量略有下降(p < 0.001)。这种变化可能是由于再生障碍性贫血患者使用了血小板生成素类似物。然而,其他非恶性适应证继续增加,最重要的是血红蛋白病的HCT增加了36%,地中海贫血和镰状细胞病的增幅相同。自2015年以来,非HCT细胞疗法增加了28%,基因改造T细胞是增长最快的细胞疗法类型。这些年度报告反映了当前的活动和趋势,对医疗保健规划很有用。