Myeloma and Lymphoma Service, West Virginia University Hospitals, Morgantown, WV, USA.
Biol Blood Marrow Transplant. 2013 Apr;19(4):625-31. doi: 10.1016/j.bbmt.2013.01.009. Epub 2013 Jan 17.
Patients with chemorefractory mantle cell lymphoma (MCL) have a poor prognosis. We used the Center for International Blood and Marrow Transplant Research database to study the outcome of 202 patients with refractory MCL who underwent allogeneic hematopoietic cell transplantation (allo-HCT) using either myeloablative (MA) or reduced-intensity/nonmyeloablative conditioning (RIC/NST), during 1998-2010. We analyzed nonrelapse mortality (NRM), progression/relapse, progression-free survival (PFS), and overall survival (OS). Seventy-four patients (median age, 54 years) received MA, and 128 patients (median age, 59 years) received RIC/NST. Median follow-up after allo-HCT was 35 months in the MA group and 43 months in the RIC/NST group. At 3 years post-transplantation, no significant between-group differences were seen in terms of NRM (47% in MA versus 43% in RIC/NST; P = .68), relapse/progression (33% versus 32%; P = .89), PFS (20% versus 25%; P = .53), or OS (25% versus 30%; P = .45). Multivariate analysis also revealed no significant between-group differences in NRM, relapse, PFS, or OS; however, receipt of a bone marrow or T cell-depleted allograft was associated with an increased risk of NRM and inferior PFS and OS. Our data suggest that despite a refractory disease state, approximately 25% of patients with MCL can attain durable remission after allo-HCT, and conditioning regimen intensity does not influence outcome of allo-HCT.
对于化疗耐药的套细胞淋巴瘤(MCL)患者,其预后较差。我们利用国际血液和骨髓移植研究中心的数据库,分析了 1998 年至 2010 年间 202 例难治性 MCL 患者接受异基因造血细胞移植(allo-HCT)的结果,这些患者采用了清髓性(MA)或减低强度/非清髓性预处理(RIC/NST)。我们分析了非复发死亡率(NRM)、进展/复发、无进展生存(PFS)和总生存(OS)。74 例患者(中位年龄 54 岁)接受 MA 预处理,128 例患者(中位年龄 59 岁)接受 RIC/NST 预处理。在 MA 组中,allo-HCT 后中位随访时间为 35 个月,在 RIC/NST 组中为 43 个月。移植后 3 年,MA 组和 RIC/NST 组在 NRM(47% vs. 43%;P=0.68)、复发/进展(33% vs. 32%;P=0.89)、PFS(20% vs. 25%;P=0.53)或 OS(25% vs. 30%;P=0.45)方面无显著组间差异。多变量分析也显示,NRM、复发、PFS 和 OS 无显著组间差异;然而,接受骨髓或 T 细胞耗竭的异基因移植物与 NRM 风险增加和 PFS 及 OS 降低相关。我们的数据表明,尽管存在难治性疾病状态,约 25%的 MCL 患者在 allo-HCT 后可获得持久缓解,预处理方案强度并不影响 allo-HCT 的结果。