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