Hallböök H, Hägglund H, Stockelberg D, Nilsson P-G, Karlsson K, Björkholm M, Linderholm M, Wahlin A, Linder O, Smedmyr B
Department of Haematology, University Hospital, Uppsala, Sweden.
Bone Marrow Transplant. 2005 Jun;35(12):1141-8. doi: 10.1038/sj.bmt.1704974.
Adult patients with acute lymphoblastic leukaemia (ALL) have been treated according to national protocols in Sweden since 1986. Stem cell transplantation (SCT) has been recommended in first remission for patients with risk factors for relapse, and for standard risk patients only after relapse. In this retrospective study, the results of autologous and allogeneic SCT in these populations were evaluated. In total, 187 patients with a median age of 34 years (17-66 years) underwent SCT. The 5-year disease-free survival (DFS), for all patients, was 26% (Confidence intervals (CI) 20-32%). The 5-year DFS was higher for patients transplanted in first remission 32% (CI 24-40%) compared to 14% (CI 5-23%; P<0.0001) in patients transplanted beyond first remission. No significant differences in DFS (P=0.06) were determined between autologous, related donor and unrelated donor SCT in the whole cohort. A lower relapse rate was counterbalanced by higher treatment-related mortality in patients undergoing allogeneic SCT. In Philadelphia-positive ALL, allogeneic SCT was superior to autologous SCT, with a 5-year DFS of 30% (CI 12-47%) vs 0% (P=0.04). Limited chronic graft-versus-host-disease (GVHD) was associated with an improved DFS of 53% (CI 38-69%) compared to no chronic GVHD of 22% (CI 10-36%; P=0.0008), indicating a clinically important graft-versus-leukaemia effect.
自1986年以来,瑞典的成年急性淋巴细胞白血病(ALL)患者一直按照国家方案进行治疗。对于有复发风险因素的患者,建议在首次缓解期进行干细胞移植(SCT),而标准风险患者仅在复发后进行。在这项回顾性研究中,评估了这些人群中自体和异基因SCT的结果。共有187例患者接受了SCT,中位年龄为34岁(17 - 66岁)。所有患者的5年无病生存率(DFS)为26%(置信区间(CI)20 - 32%)。首次缓解期接受移植的患者5年DFS较高,为32%(CI 24 - 40%),而首次缓解期后接受移植的患者为14%(CI 5 - 23%;P<0.0001)。在整个队列中,自体、相关供体和无关供体SCT之间的DFS无显著差异(P = 0.06)。异基因SCT患者的复发率较低,但治疗相关死亡率较高。在费城染色体阳性的ALL中,异基因SCT优于自体SCT,5年DFS分别为30%(CI 12 - 47%)和0%(P = 0.04)。与无慢性移植物抗宿主病(GVHD)的患者22%(CI 10 - 36%)相比,有限的慢性GVHD与改善的DFS 53%(CI 38 - 69%)相关(P = 0.0008),表明存在临床上重要的移植物抗白血病效应。