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Non-myeloablative Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Relapsed and Refractory Mantle Cell Lymphoma: A Single Center Analysis in the Rituximab Era

机译:成人非复发性异基因造血干细胞移植治疗复发性和难治性套细胞淋巴瘤:利妥昔单抗时代的单中心分析。

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摘要

Relapsed and refractory (rel/ref) mantle cell lymphoma (MCL) portends a dismal prognosis. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) represents the only potentially curative therapy in this setting. We analyzed survival outcomes of 29 recipients of non-myeloablative allo-HSCT for rel/ref MCL, and studied possible prognostic factors in this setting. The cumulative incidence of disease progression and non-relapse mortality at 3 years were 28% (95% confidence interval [CI]: 13-46%) and 29% (95%CI: 13-47%), respectively. The cumulative incidence of grade II-IV acute graft-versus-host disease (GVHD) at days +100 and +180 were 34% (95%CI: 18-52%) and 45% (95%CI: 26-62%), respectively. With a median follow-up in survivors of 53 (range 24-83) months, the 3-year overall survival (OS) and progression-free survival (PFS) were 54% (95%CI: 38-76%) and 41% (95%CI: 26-64%), respectively. In vivo T-cell depletion with alemtuzumab (n=6) was associated with inferior 3-year PFS (0% vs. 51%, p=0.007) and OS (17% vs. 64%, p=0.014). Conversely, a second line international prognostic index (sIPI) at transplantation equal to 0 (no risk factors) was associated with an improved 3-year PFS (52% vs. 22%, p=0.020) and OS (71% vs. 22%, p=0.006) compared to sIPI ≥1. Performing an allo-HSCT before 2007 was associated with a decreased 3-year OS (25% vs. 76%, p=0.015) but not with a significantly inferior PFS (17% vs. 59%, p=0.058). In this single center series, we report encouraging results with allo-HSCT for patients with rel/ref MCL. High alemtuzumab doses should probably be avoided in this context.
机译:复发性和难治性(rel / ref)套细胞淋巴瘤(MCL)预后不良。同种异体造血干细胞移植(allo-HSCT)是这种情况下唯一可能治愈的疗法。我们分析了29例非清髓性异体-HSCT受体的rel / ref MCL的生存结果,并研究了这种情况下可能的预后因素。 3年时疾病进展和非复发死亡率的累积发生率分别为28%(95%置信区间[CI]:13-46%)和29%(95%CI:13-47%)。第100天和+180天时,II-IV级急性移植物抗宿主病(GVHD)的累积发生率分别为34%(95%CI:18-52%)和45%(95%CI:26-62%) ), 分别。对幸存者进行的中位随访时间为53(24-83)个月,其3年总生存(OS)和无进展生存(PFS)分别为54%(95%CI:38-76%)和41 %(95%CI:26-64%)。体内使用Alemtuzumab的T细胞耗竭(n = 6)与3年级PFS(0%vs. 51%,p = 0.007)和OS(17%vs. 64%,p = 0.014)相关。相反,移植时的二线国际预后指数(sIPI)等于0(无危险因素)与3年PFS(52%vs. 22%,p = 0.020)和OS(71%vs. 22)改善相关。 %,p = 0.006),而sIPI≥1。在2007年之前进行all-HSCT与3年OS降低有关(25%比76%,p = 0.015),但与PFS明显不佳(17%vs. 59%,p = 0.058)无关。在这个单一中心的系列文章中,我们报道了针对rel / ref MCL患者的allo-HSCT结果令人鼓舞。在这种情况下,应避免使用高剂量的alemtuzumab。

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