Tabbara Imad A, Zimmerman Kathy, Morgan Connie, Nahleh Zeina
Bone Marrow Transplant Program, University of Virginia Health System, PO Box 800716, Charlottesville, VA 22908-0716, USA.
Arch Intern Med. 2002 Jul 22;162(14):1558-66. doi: 10.1001/archinte.162.14.1558.
Acute complications such as veno-occlusive disease of the liver, acute and chronic graft-vs-host disease (GVHD), and infectious conditions remain major obstacles for the success of allogeneic hematopoietic stem cell transplantation (HSCT). Progress in allogeneic HSCT depends on several factors, including the adequate prevention and management of associated complications, advances in the conventional management of diseases currently treated with allogeneic HSCT, expansion of the donor pool, selective control of GVHD, development of more effective preparative regimens to eradicate the neoplastic cell population, characterization of a new generation of hematopoietic growth factors and cytokines, and development of newer techniques for ex vivo manipulation of stem cells. Hematopoietic growth factor-mobilized donor progenitor cells collected from peripheral blood have been shown to be associated with rapid hematopoietic engraftment without an increase in the incidence of acute GVHD compared with allogeneic bone marrow transplantation. Implementation of this approach will enhance donor acceptance, eliminate the risk of general anesthesia, decrease cost, and reduce the risk of infectious complications by reducing the duration of neutropenia. Nonmyeloablative allogeneic stem cell transplantation represents a novel treatment approach that may lead to reduced toxic effects and extended use of this treatment in older patients and in those with malignant and nonmalignant disorders. However, GVHD and disease recurrence remain a challenge. Promising results have been reported in patients with refractory hematologic malignancies and in metastatic renal cell cancer. Because late complications are commonly encountered in patients receiving allogeneic HSCT, lifelong observation is needed.
急性并发症,如肝静脉闭塞病、急慢性移植物抗宿主病(GVHD)和感染性疾病,仍然是异基因造血干细胞移植(HSCT)成功的主要障碍。异基因HSCT的进展取决于多个因素,包括相关并发症的充分预防和管理、目前采用异基因HSCT治疗的疾病传统管理方法的进展、供者库的扩大、GVHD的选择性控制、开发更有效的预处理方案以根除肿瘤细胞群体、新一代造血生长因子和细胞因子的特性鉴定,以及开发更新的体外干细胞操作技术。与异基因骨髓移植相比,从外周血收集的造血生长因子动员的供者祖细胞已被证明与快速造血植入相关,且急性GVHD的发生率没有增加。采用这种方法将提高供者的接受度,消除全身麻醉的风险,降低成本,并通过缩短中性粒细胞减少的持续时间降低感染并发症的风险。非清髓性异基因干细胞移植是一种新的治疗方法,可能会减少毒性作用,并扩大该治疗在老年患者以及患有恶性和非恶性疾病患者中的应用。然而,GVHD和疾病复发仍然是一个挑战。在难治性血液系统恶性肿瘤患者和转移性肾细胞癌患者中已报道了有希望的结果。由于接受异基因HSCT的患者常出现晚期并发症,因此需要终身观察。