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Use of haploidentical stem cell transplantation continues to increase: the 2015 European Society for Blood and Marrow Transplant activity survey report.

机译:半相合干细胞移植的使用继续增加:2015年欧洲血液和骨髓移植协会活动调查报告。

摘要

Hematopoietic stem cell transplantation (HSCT) is an established procedure for many acquired and congenital disorders of the hematopoietic system. A record number of 42 171 HSCT in 37 626 patients (16 030 allogeneic (43%), 21 596 autologous (57%)) were reported by 655 centers in 48 countries in 2015. Trends include continued growth in transplant activity over the last decade, with the highest percentage increase seen in middle-income countries but the highest absolute growth in the very-high-income countries in Europe. Main indications for HSCT were myeloid malignancies 9413 (25%; 96% allogeneic), lymphoid malignancies 24 304 (67%; 20% allogeneic), solid tumors 1516 (4%; 3% allogeneic) and non-malignant disorders 2208 (6%; 90% allogeneic). Remarkable is the decreasing use of allogeneic HSCT for CLL from 504 patients in 2011 to 255 in 2015, most likely to be due to new drugs. Use of haploidentical donors for allogeneic HSCT continues to grow: 2012 in 2015, a 291% increase since 2005. Growth is seen for all diseases. In AML, haploidentical HSCT increases similarly for patients with advanced disease and for those in CR1. Both marrow and peripheral blood are used as the stem cell source for haploidentical HSCT with higher numbers reported for the latter.Bone Marrow Transplantation advance online publication, 13 March 2017; doi:10.1038/bmt.2017.34.
机译:造血干细胞移植(HSCT)是许多后天性和先天性造血系统疾病的既定程序。 2015年,在48个国家/地区的655个中心报告了37 626例患者中42 171例HSCT的创纪录数量(16 030例同种异体(43%),21 596例自体(57%))。 ,其中中等收入国家的百分比增长率最高,但欧洲超高收入国家的绝对增长率最高。 HSCT的主要适应症是髓系恶性肿瘤9413(25%; 96%同种异体),淋巴恶性肿瘤24 304(67%; 20%同种异体),实体瘤1516(4%; 3%同种异体)和非恶性疾病2208(6% ; 90%同种异体)。值得注意的是,异基因HSCT用于CLL的使用从2011年的504名患者减少到2015年的255名,这很可能是由于新药引起的。单倍体供体用于异基因HSCT的使用持续增长:2012年到2015年,自2005年以来增加了291%。在AML中,单发性HSCT对于晚期疾病患者和CR1患者相似。骨髓和外周血均用作单倍体HSCT的干细胞来源,据报道后者数量更高.2017年3月13日在线出版的《骨髓移植》; doi:10.1038 / bmt.2017.34。

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