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自体移植失败后首次复发的多发性骨髓瘤患者中供者与非供者比较的长期随访。

Long-Term Follow-Up of a Donor versus No-Donor Comparison in Patients with Multiple Myeloma in First Relapse after Failing Autologous Transplantation.

机构信息

Department of Hematology, DAME, University of Udine, Udine, Italy.

Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy; Department of Oncology, Presidio Molinette, AOU Città della Salute e della Scienza di Torino, Torino, Italy.

出版信息

Biol Blood Marrow Transplant. 2018 Feb;24(2):406-409. doi: 10.1016/j.bbmt.2017.10.014. Epub 2017 Oct 12.

DOI:10.1016/j.bbmt.2017.10.014
PMID:29032267
Abstract

We report the long-term clinical outcomes of a retrospective multicenter study that enrolled 169 patients with multiple myeloma (MM) in first relapse after failing autologous stem cell transplantation (SCT). After HLA typing at relapse, 79 patients with a suitable donor, 72 (91%) of whom eventually underwent salvage allogeneic SCT (allo-SCT), were compared with 90 patients without a donor who were treated with multiple lines of salvage treatment with bortezomib and/or immunomodulatory agents. At a median follow-up of 30 months (range, 2-180 months) for all patients and 110 months (range, 38-180 months) for surviving patients, 7-year progression-free survival (PFS) was 18% in the donor group and 0% in the no-donor group (hazard ratio [HR], 2.495; 95% confidence interval [CI], 1.770-3.517; P < .0001). Seven-year overall survival (OS) was 31% in the donor group and 9% in the no-donor group (HR, 1.835; 95% CI, 1.306-2.577; P < .0001). By multivariate analysis, chemosensitivity to salvage treatments and presence of a suitable donor were significantly associated with better PFS and OS. The long-term follow-up of this study confirms the significant PFS benefit and provides new evidence of an OS advantage for patients with MM who have a suitable donor and undergo allo-SCT. Allo-SCT should be considered as a treatment option in young relapsed patients with high-risk disease features after first-line treatment.

摘要

我们报告了一项回顾性多中心研究的长期临床结果,该研究纳入了 169 例在自体干细胞移植(SCT)后复发的多发性骨髓瘤(MM)患者。在复发时进行 HLA 分型后,79 例有合适供体的患者,其中 72 例(91%)最终接受了挽救性异体 SCT(allo-SCT),与 90 例无供体的患者进行了比较,这些患者接受了硼替佐米和/或免疫调节剂的多线挽救治疗。在所有患者的中位随访 30 个月(范围 2-180 个月)和存活患者的中位随访 110 个月(范围 38-180 个月)中,供体组的 7 年无进展生存率(PFS)为 18%,无供体组为 0%(风险比[HR],2.495;95%置信区间[CI],1.770-3.517;P<0.0001)。供体组的 7 年总生存率(OS)为 31%,无供体组为 9%(HR,1.835;95%CI,1.306-2.577;P<0.0001)。通过多变量分析,挽救治疗的化疗敏感性和合适供体的存在与更好的 PFS 和 OS 显著相关。本研究的长期随访证实了 PFS 的显著获益,并为具有合适供体并接受 allo-SCT 的 MM 患者提供了 OS 优势的新证据。allo-SCT 应被视为一线治疗后具有高危疾病特征的年轻复发患者的治疗选择。

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