Donato Michele L, Siegel David S, Vesole David H, McKiernan Phyllis, Nyirenda Themba, Pecora Andrew L, Baker Melissa, Goldberg Stuart L, Mato Anthony, Goy Andre, Rowley Scott D
John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
Biol Blood Marrow Transplant. 2014 Aug;20(8):1211-6. doi: 10.1016/j.bbmt.2014.04.027. Epub 2014 May 2.
We conducted a study of patients with multiple myeloma (MM) undergoing allogeneic transplantation to evaluate outcome parameters. Fifty-seven consecutive patients with MM received an allogeneic transplantation between 2004 and 2011 at our institution. Patients who had received at least 1 prior autologous transplantation were included. Twenty-six patients underwent allogeneic transplantation for consolidation after a response to their first autograft, and 30 patients received an allogeneic transplantation as salvage therapy. Donor source was evenly distributed between related and unrelated. The median follow-up was 52 months. Thirty-two (57.1%) patients achieved a complete response (CR). At 5 years, 49.2% of all patients were in CR. Sixteen patients received either donor lymphocyte infusions or immune suppression withdrawal for disease progression, with a 62.5% response rate. The 5-year overall survival (OS) for all patients was 59%. The 5-year OS for the 30 patients in the consolidation group was 82% compared with 38% for those in the salvage group. In multivariate analysis, 3 factors remained significantly associated with OS. These include being in the salvage group (hazard ratio [HR], 4.05; P = .0196), acute graft-versus-host disease (aGVHD) (HR, 2.99; P = .034), and chronic graft-versus-host disease (cGVHD), which was highly protective, with a 5-year OS of 78.8% for patients with cGVHD versus 42.6% for patients without cGVHD (HR .17, P = .008). Our data show that allogeneic transplantation for MM can lead to sustained remissions. aGVHD is significantly deleterious to OS and progression-free survival, whereas cGVHD is strongly favorable, supporting an important role for the graft-versus-myeloma effect.
我们对接受异基因移植的多发性骨髓瘤(MM)患者进行了一项研究,以评估预后参数。2004年至2011年期间,我们机构有57例连续的MM患者接受了异基因移植。纳入至少接受过1次自体移植的患者。26例患者在首次自体移植缓解后接受异基因移植巩固治疗,30例患者接受异基因移植作为挽救治疗。供体来源在亲属和非亲属之间均匀分布。中位随访时间为52个月。32例(57.1%)患者达到完全缓解(CR)。5年时,所有患者中有49.2%处于CR状态。16例患者因疾病进展接受了供体淋巴细胞输注或免疫抑制撤除治疗,缓解率为62.5%。所有患者的5年总生存率(OS)为59%。巩固组30例患者的5年OS为82%,而挽救组为38%。在多变量分析中,3个因素仍与OS显著相关。这些因素包括处于挽救组(风险比[HR],4.05;P = .0196)、急性移植物抗宿主病(aGVHD)(HR,2.99;P = .034)以及慢性移植物抗宿主病(cGVHD),后者具有高度保护作用,有cGVHD的患者5年OS为78.8%,无cGVHD的患者为42.6%(HR .17,P = .008)。我们的数据表明,MM的异基因移植可导致持续缓解。aGVHD对OS和无进展生存期有显著不利影响,而cGVHD则非常有利,支持移植物抗骨髓瘤效应的重要作用。