Department for Stem Cell Transplantation, University of Hamburg, 20246 Hamburg, Germany.
Blood. 2012 Nov 15;120(20):4256-62. doi: 10.1182/blood-2012-06-436725. Epub 2012 Sep 24.
The best conditioning regimen before allogeneic transplantation for high-risk diffuse large B-cell lymphoma (DLBCL) remains to be clarified. We analyzed data from 396 recipients of allotransplants for DLBCL receiving myeloablative (MAC; n = 165), reduced intensity (RIC; n = 143), or nonmyeloablative conditioning (NMAC; n = 88) regimens. Acute and chronic GVHD rates were similar across the groups. Five-year nonrelapse mortality (NRM) was higher in MAC than RIC and NMAC (56% vs 47% vs 36%; P = .007). Five-year relapse/progression was lower in MAC than in RIC/NMAC (26% vs 38% vs 40%; P = .031). Five-year progression-free survival (15%-25%) and overall survival (18%-26%) did not differ significantly between the cohorts. In multivariate analysis, NMAC and more recent transplant year were associated with lower NRM, whereas a lower Karnofsky performance score (< 90), prior relapse resistant to therapy, and use of unrelated donors were associated with higher NRM. NMAC transplants, no prior use of rituximab, and prior relapse resistant to therapy were associated with a greater risk of relapse/progression. In conclusion, allotransplantation with RIC or NMAC induces long-term progression-free survival in selected DLBCL patients with a lower risk of NRM but with higher risk of lymphoma progression or relapse.
在接受异基因移植治疗高危弥漫性大 B 细胞淋巴瘤 (DLBCL) 之前,哪种预处理方案最佳尚不清楚。我们分析了 396 例接受异基因移植治疗 DLBCL 患者的数据,这些患者接受了清髓性(MAC;n = 165)、减低强度(RIC;n = 143)或非清髓性(NMAC;n = 88)预处理方案。各组患者的急性和慢性移植物抗宿主病(GVHD)发生率相似。MAC 组的 5 年非复发死亡率(NRM)高于 RIC 和 NMAC 组(56%比 47%比 36%;P =.007)。MAC 组的 5 年复发/进展率低于 RIC/NMAC 组(26%比 38%比 40%;P =.031)。5 年无进展生存率(15%-25%)和总生存率(18%-26%)在各队列间无显著差异。多变量分析显示,NMAC 和较晚的移植年份与较低的 NRM 相关,而 Karnofsky 表现评分较低(< 90)、先前治疗抵抗的复发以及使用无关供者与较高的 NRM 相关。NMAC 移植、先前未使用利妥昔单抗以及先前治疗抵抗的复发与更高的复发/进展风险相关。总之,RIC 或 NMAC 异基因移植在选择的 DLBCL 患者中诱导长期无进展生存,NRM 风险较低,但淋巴瘤进展或复发风险较高。