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Long-term survival and polyclonal immunoglobulin reconstitution after allogeneic stem cell transplantation in multiple myeloma

机译:在多种骨髓瘤中同种异体干细胞移植后的长期存活和多克隆免疫球蛋白重构

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Despite significant progress made in the treatment of patients with multiple myeloma (MM) in the last decade, for patients with early relapse or rapidly progressing high-risk disease, allogeneic hematopoietic stem cell transplantation (SCT) might be an option leading to long-term survival. Here, we retrospectively analyzed the outcomes of 90 MM patients who received allogeneic SCT in our center between 1999 and 2017. We specifically assessed the association of impaired humoral immune reconstitution, referred to as immunoparesis, and post-transplant survival. Sixty-four patients received allogeneic SCT in relapse following 2-7 lines of therapy; 26 patients received upfront tandem autologous-allogeneic SCT. With a median follow-up of 76 months, OS and PFS were 52.6% (95% CI 42.9-64.3) and 36.4% (95% CI 27.6-47.9) at 2 years and 38.6% (95% CI 29.2-51.1) and 25.3% (95% CI 17.5-36.4) at 5 years, respectively. Receiving more than two therapy lines prior to transplantation was an independent risk factor for OS (HR 3.68, 95% CI 2.02-6.70) and PFS (HR 3.69, 95% CI 2.09-6.50). In a landmark analysis at day 200, prolonged immunoparesis was associated with reduced OS (HR 3.22, 95% CI 1.14-9.11). Allogeneic stem cell transplantation offers an additional treatment element that may lead to long-term remission in selected patients with poor prognosis, probably exploiting graft-versus-myeloma effects. Immunoparesis could potentially serve as an indicator for impaired survival following allogeneic transplantation, an observation to be further studied prospectively.
机译:尽管在过去十年中治疗多发性骨髓瘤(mm)的患者进行了显着进展,对于早期复发或迅速进展的高危疾病,但同种异体造血干细胞移植(SCT)可能是一个长期的选项生存。在这里,我们回顾性地分析了1999年至2017年期间在我们的中心接受同种异体SCT的90毫米患者的结果。我们特别评估了体液免疫重建受损的关联,称为免疫血清,以及移植后的存活。六十四名患者接受两种治疗后两种术治疗后复发; 26例患者接受前期串联自体相生SCT。在76个月的中间随访中,OS和PFS为52.6%(95%CI 42.9-64.3)和36.4%(95%CI 27.6-47.9),2年,38.6%(95%CI 29.2-51.1)和5年分别为25.3%(95%CI 17.5-36.4)。在移植之前接受两条以上的治疗系是OS的独立危险因素(HR 3.68,95%CI 2.02-6.70)和PFS(HR 3.69,95%CI 2.09-6.50)。在第200天的地标分析中,延长的免疫法与减少的OS(HR 3.22,95%CI 1.14-9.11)有关。同种异体干细胞移植提供了一种额外的治疗组件,可导致选定患者的长期缓解患者预后差,可能是利用移植物与骨髓瘤效应。免疫缺失可能用作同种异体移植后存活损害的指标,预期将进一步研究进一步研究。

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