Department of Hematology, CHU, Strasbourg, France.
Blood. 2012 Mar 22;119(12):2943-8. doi: 10.1182/blood-2011-05-352989. Epub 2012 Feb 9.
The LAM2001 phase 3 trial, involving 832 patients with acute myeloid leukemia (AML; median: 46 years) proposed HLA-identical sibling allograft HSCT for all patients with an identified donor. The trial compared reduced-intensity conditioning (RIC) for patients older than 50 years of age (N = 47) and myeloablative conditioning for younger patients (N = 117). BM HSCT was performed in the younger patients, while the older ones received a consolidation course, followed by peripheral blood allo-HSCT using RIC. The incidence of grade II-IV acute GVHD, was 51.9% (95% confidence interval [CI]: 42.1-61.8) and 11.3% (1.6-21.2) after myeloablative or RIC, respectively (P < .0001) and that of chronic GVHD 45.8% (95% CI: 34.8-56.7) and 41.7% (24.7-58.6; NS). Cumulative incidence of nonrelapse mortality at 108 months was 15.8% (95% CI: 9.8-23.2) for myeloablative, and 6.5% (0.2-16.2) for RIC (NS). CI of relapse at 108 months was 21.7% (95% CI: 13.9-28.6) and 28.6% (16.5-43.4; NS). Overall survival at 108 months was 63.4% (95% CI: 54.6-72.2) and 65.8% (52.2-72.2), respectively, after myeloablative or RIC (NS). RIC peripheral blood stem cell allo-HSCT is prospectively feasible for patients between the ages of 51 and 60 years without excess of relapse or nonrelapse mortality, and compares favorably with myeloablative marrow allo-HSCT proposed to younger patients.
LAM2001 期 3 试验纳入 832 例急性髓细胞白血病(AML;中位年龄:46 岁)患者,提出对所有有供者的患者进行 HLA 相同的同胞异基因造血干细胞移植(HSCT)。该试验比较了年龄大于 50 岁患者(n=47)的减低强度预处理(RIC)和年龄较小患者(n=117)的清髓性预处理。年轻患者行 BM HSCT,年龄较大患者先行巩固治疗,然后采用 RIC 行外周血异基因 HSCT。RIC 后,Ⅱ-Ⅳ级急性移植物抗宿主病的发生率为 51.9%(95%CI:42.1-61.8),而清髓性预处理后为 11.3%(1.6-21.2)(P<0.0001),慢性移植物抗宿主病的发生率为 45.8%(95%CI:34.8-56.7)和 41.7%(24.7-58.6;NS)。108 个月时非复发死亡率的累积发生率,清髓性预处理组为 15.8%(95%CI:9.8-23.2),RIC 组为 6.5%(0.2-16.2)(NS)。108 个月时的复发累积发生率,清髓性预处理组为 21.7%(95%CI:13.9-28.6),RIC 组为 28.6%(16.5-43.4;NS)。108 个月时的总生存率,清髓性预处理组为 63.4%(95%CI:54.6-72.2),RIC 组为 65.8%(52.2-72.2),两组之间无统计学差异(NS)。RIC 外周血造血干细胞异基因 HSCT 对于年龄在 51-60 岁的患者是一种可行的方案,不增加复发或非复发死亡率,并且与建议年轻患者进行的清髓性骨髓异基因 HSCT 相比具有优势。