Clinical Research Division, Fred Hutchinson Cancer Research Center, USA.
Best Pract Res Clin Haematol. 2012 Dec;25(4):465-71. doi: 10.1016/j.beha.2012.10.009. Epub 2012 Oct 25.
Over the last 2 decades, there have been a number of changes in clinical practice that individually could affect the outcome of allogeneic hematopoietic cell transplantation (HCT), but until recently the collective impact of these changes was unknown. Accordingly, several groups asked the question of whether the outcome of allogeneic HCT has improved, and if so, why. Four large studies including a total of more than 10,000 patients have been performed and have reached very similar conclusions. Compared to transplants performed in the 1990s, the hazard ratio for nonrelapse mortality for transplants performed in the 2000s was roughly 0.5. This remarkable improvement was seen when the analyses were restricted to myeloablative transplants, to recipients of marrow rather than peripheral blood, or to transplants from matched siblings, and persisted after analyses were adjusted for patient risk. Likely explanations for this improvement include the avoidance of the most toxic preparative regimens, use of agents that spare hepatic and renal function, and improved methods for control of infections.
在过去的 20 年中,临床实践发生了许多变化,这些变化可能会单独影响异基因造血细胞移植(HCT)的结果,但直到最近,这些变化的综合影响仍不得而知。因此,有几个小组提出了这样一个问题:异基因 HCT 的结果是否有所改善,如果有,原因是什么。已经进行了四项包括超过 10000 名患者的大型研究,得出了非常相似的结论。与 20 世纪 90 年代进行的移植相比,21 世纪进行的移植中非复发死亡率的风险比约为 0.5。当分析仅限于清髓性移植、骨髓而非外周血供者的移植,或来自匹配同胞的移植时,以及在调整患者风险后进行分析时,都可以看到这种显著的改善。这种改善的可能解释包括避免使用毒性最大的预处理方案、使用可保护肝肾功能的药物,以及改进感染控制方法。