Vigouroux Stéphane, Michallet Mauricette, Porcher Raphaël, Attal Michel, Ades Lionel, Bernard Marc, Blaise Didier, Tabrizi Reza, Garban Frédéric, Cassuto Jill-Patrice, Chevalier Patrice, Facon Thierry, Ifrah Norbert, Renaud Marc, Tilly Hervé, Vernant Jean-Paul, Kuentz Mathieu, Bourhis Jean-Henri, Bordigoni Pierre, Deconinck Eric, Lioure Bruno, Socié Gérard, Milpied Noël
Service d'Hématologie Clinique, Centre Hospitalier Universitaire (CHU) Pontchaillou, Rennes, France.
Haematologica. 2007 May;92(5):627-34. doi: 10.3324/haematol.10924.
High-dose chemotherapy with allogeneic stem cell transplantation (SCT) has proven to be a successful treatment for low-grade lymphoma (LGL), but is associated with considerable transplant-related mortality (TRM). In an effort to reduce toxic mortality while maintaining the graft-versus-leukemia effect, allogeneic SCT has been combined with a reduced-intensity conditioning (RIC) regimen. The aim of this study was to determine the outcome of patients with LGL treated with RIC allogeneic SCT.
This retrospective multicenter study included 73 patients with relapsed or refractory LGL allografted after a RIC regimen between 1998 and 2005 whose data were recorded in a French registry.
Patients received a median of three lines of therapy prior to RIC allogeneic SCT. The most widely used conditioning regimens were fludarabine + busulfan + antithymocyte globulin (n=43) and fludarabine + total body irradiation (n=21). Prior to allografting, patients were in complete response (CR; n=21), partial response (PR; n=33) or had chemoresistant disease (n=19). The median follow-up was 37 months (range, 16 to 77 months). In patients in CR, PR and chemoresistant disease, the 3-year overall survival rates were 66%, 64% and 32%, respectively, while the 3-year event-free survival rates were 66%, 52% and 32%, respectively. The 3-year cumulative incidences of TRM were 32%, 28% and 63%, respectively. The incidence of relapse was 9.6%.
Although associated with significant TRM, RIC allogeneic SCT in advanced chemosensitive disease leads to long-term survival.
高剂量化疗联合异基因干细胞移植(SCT)已被证明是治疗低度淋巴瘤(LGL)的一种成功方法,但与相当高的移植相关死亡率(TRM)相关。为了在维持移植物抗白血病效应的同时降低毒性死亡率,异基因SCT已与降低强度预处理(RIC)方案联合使用。本研究的目的是确定接受RIC异基因SCT治疗的LGL患者的预后。
这项回顾性多中心研究纳入了1998年至2005年间接受RIC方案后进行异基因移植的73例复发或难治性LGL患者,其数据记录在法国的一个登记处。
患者在接受RIC异基因SCT之前接受的治疗中位数为三线。最常用的预处理方案是氟达拉滨+白消安+抗胸腺细胞球蛋白(n = 43)和氟达拉滨+全身照射(n = 21)。在进行同种异体移植之前,患者处于完全缓解(CR;n = 21)、部分缓解(PR;n = 33)或化疗耐药疾病(n = 19)状态。中位随访时间为37个月(范围为16至77个月)。在CR、PR和化疗耐药疾病患者中,3年总生存率分别为66%、64%和32%,而3年无事件生存率分别为66%、52%和32%。TRM的3年累积发生率分别为32%、28%和63%。复发率为9.6%。
尽管与显著的TRM相关,但在晚期化疗敏感疾病中,RIC异基因SCT可导致长期生存。