异基因造血干细胞移植治疗慢性淋巴细胞白血病:20 年队列研究结果。
Allogeneic haematopoietic stem cell transplantation for chronic lymphocytic leukaemia: outcome in a 20-year cohort.
机构信息
Division of Hematology, Leukemia/BMT Program of British Columbia, Vancouver General Hospital, BC Cancer Agency, University of British Columbia, Vancouver, BC.
Cytogenetics Laboratory, Department of Pathology and Laboratory Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC.
出版信息
Br J Haematol. 2012 Jul;158(2):174-185. doi: 10.1111/j.1365-2141.2012.09170.x. Epub 2012 May 29.
The curative potential of allogeneic haematopoietic stem cell transplant (allo HSCT) in chronic lymphocytic leukaemia CLL is established, with a demonstrated role for graft-versus-leukaemia and less certainty for other factors in determining outcome. The first two decades of CLL patients proceeding to allo HSCT at the Leukaemia/Bone Marrow Transplant Program of British Columbia (n = 49 consecutive, 1991-2009) were studied to clarify factors predicting outcome. The donor was related in 29 (59%) and unrelated in 20 (41%). Conditioning was reduced-intensity in 27 (55%) and myeloablative in 22 (45%). Thirty-one of 49 patients survive with median follow-up of 5 years (0·2-15). Cumulative incidence of non-relapse mortality; complete remission (CR); clearance of fluorescence in situ hybridization (FISH) abnormality and progression at 10 years was 36%; 69%; 55% and 22%. Overall survival (OS) was 63% at 2 years; 55% at 5 years and beyond. Factors predicting OS (P value by log rank <0·05) were: comorbidity index <3, FISH rank (Dohner) and 17p deletion, alemtuzumab pre-HSCT, achievement of CR post-HSCT, donor chimerism >90%, clearance of FISH abnormality post-HSCT and absence of high-grade (3-4) graft-versus-host disease. Results from this province-wide, two-decade cohort demonstrated that a substantial proportion of patients with high-risk CLL become long term disease-free survivors.
同种异体造血干细胞移植 (allo HSCT) 在慢性淋巴细胞白血病 (CLL) 中的治疗潜力已得到证实,移植物抗白血病作用已得到证明,而其他因素在确定预后方面的作用则不太确定。为了阐明预测结果的因素,对不列颠哥伦比亚白血病/骨髓移植项目 (n = 49 例连续患者,1991-2009 年) 中进行 allo HSCT 的前 20 年 CLL 患者进行了研究。供者在 29 例(59%)中为亲属,在 20 例(41%)中为无关供者。预处理方案为低强度 27 例(55%),高强度 22 例(45%)。49 例患者中有 31 例存活,中位随访时间为 5 年(0.2-15 年)。非复发死亡率、完全缓解 (CR)、荧光原位杂交 (FISH) 异常清除和 10 年进展的累积发生率分别为 36%、69%、55%和 22%。2 年时总生存率 (OS) 为 63%,5 年及以上时为 55%。预测 OS 的因素(对数秩检验 P 值<0.05)为:合并症指数 <3、FISH 分级(多纳)和 17p 缺失、allo HSCT 前阿仑单抗、allo HSCT 后获得 CR、供者嵌合率 >90%、allo HSCT 后 FISH 异常清除和无高级(3-4 级)移植物抗宿主病。这项全省范围内、为期 20 年的队列研究结果表明,相当一部分高危 CLL 患者成为长期无病幸存者。