Fred Hutchinson Cancer Research Center and the University of Washington School of Medicine, Seattle, WA, USA.
Expert Rev Hematol. 2010 Jun;3(3):285-99. doi: 10.1586/ehm.10.21.
Allogeneic hematopoietic cell transplantation (HCT) is a potentially curative procedure for a variety of hematologic malignancies. The field has evolved substantially over the past decade, with advances in patient and donor selection, stem cell sources, supportive care, prevention of complications and reduced-toxicity preparative regimens. As a result, the indications for HCT and the pool of eligible patients have expanded significantly. In this article, we provide an overview of the major aspects of allogeneic HCT, and focus specifically on areas of active research and on novel approaches to challenges in the field. Specifically, we will discuss approaches to reduce the toxicity of the preparative regimen, with the goal of increasing the safety and applicability of HCT. The availability of suitable donors may be an obstacle to wider application of HCT. We review three major approaches to broadening the donor pool: the use of HLA-mismatched unrelated donors, umbilical cord blood and HLA-haploidentical family donors. Graft-versus-host disease remains a major cause of morbidity and mortality after HCT. We review recent advances in the understanding of this phenomenon, and novel prophylactic and therapeutic approaches that hold the promise of further improving the safety of the procedure. We conclude with a speculative outline of the next 5 years of research in the field of HCT.
异基因造血细胞移植(HCT)是治疗多种血液系统恶性肿瘤的潜在治愈方法。在过去的十年中,该领域取得了实质性的进展,包括患者和供者选择、干细胞来源、支持性护理、并发症预防以及降低毒性的预处理方案等方面的进步。因此,HCT 的适应证和合格患者群体显著扩大。在本文中,我们概述了异基因 HCT 的主要方面,并特别关注该领域的活跃研究领域和新的挑战方法。具体而言,我们将讨论降低预处理方案毒性的方法,以提高 HCT 的安全性和适用性。合适供者的可用性可能是限制 HCT 更广泛应用的一个障碍。我们回顾了扩大供者群体的三种主要方法:使用 HLA 不合的无关供者、脐带血和 HLA 半相合家族供者。移植物抗宿主病仍然是 HCT 后发病率和死亡率的主要原因。我们回顾了对这种现象的理解的最新进展,以及有希望进一步提高该过程安全性的新型预防和治疗方法。最后,我们对 HCT 领域未来 5 年的研究进行了推测性概述。