Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, California.
Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Biol Blood Marrow Transplant. 2018 Mar;24(3):478-485. doi: 10.1016/j.bbmt.2017.10.024. Epub 2017 Oct 24.
We compared postrelapse overall survival (OS) after autologous/allogeneic (auto/allo) versus tandem autologous (auto/auto) hematopoietic cell transplantation (HCT) in patients with multiple myeloma (MM). Postrelapse survival of patients receiving an auto/auto or auto/allo HCT for MM and prospectively reported to the Center for International Blood and Marrow Transplant Research between 2000 and 2010 were analyzed. Relapse occurred in 404 patients (72.4%) in the auto/auto group and in 178 patients (67.4%) in the auto/allo group after a median follow-up of 8.5 years. Relapse occurred before 6 months after a second HCT in 46% of the auto/allo patients, compared with 26% of the auto/auto patients. The 6-year postrelapse survival was better in the auto/allo group compared with the auto/auto group (44% versus 35%; P = .05). Mortality due to MM was 69% (n = 101) in the auto/allo group and 83% (n = 229) deaths in auto/auto group. In multivariate analysis, both cohorts had a similar risk of death in the first year after relapse (hazard ratio [HR], .72; P = .12); however, for time points beyond 12 months after relapse, overall survival was superior in the auto/allo cohort (HR for death in auto/auto =1.55; P = .005). Other factors associated with superior survival were enrollment in a clinical trial for HCT, male sex, and use of novel agents at induction before HCT. Our findings shown superior survival afterrelapse in auto/allo HCT recipients compared with auto/auto HCT recipients. This likely reflects a better response to salvage therapy, such as immunomodulatory drugs, potentiated by a donor-derived immunologic milieu. Further augmentation of the post-allo-HCT immune system with new immunotherapies, such as monoclonal antibodies, checkpoint inhibitors, and others, merit investigation.
我们比较了多发性骨髓瘤(MM)患者接受自体/异体(auto/allo)与串联自体(auto/auto)造血细胞移植(HCT)后的复发后总体生存(OS)。分析了 2000 年至 2010 年期间向国际血液和骨髓移植研究中心前瞻性报告的接受 auto/auto 或 auto/allo HCT 治疗的 MM 患者的复发后生存情况。在中位随访 8.5 年后,auto/auto 组中有 404 例(72.4%)患者和 auto/allo 组中有 178 例(67.4%)患者发生复发。在 auto/allo 患者中,46%的患者在第二次 HCT 后 6 个月内复发,而在 auto/auto 患者中这一比例为 26%。与 auto/auto 组相比,auto/allo 组的 6 年复发后生存率更好(44% vs 35%;P=0.05)。在 auto/allo 组中,死于 MM 的患者有 101 例(69%),而在 auto/auto 组中,死于 MM 的患者有 229 例(83%)。多变量分析显示,两组患者在复发后第一年的死亡风险相似(危险比[HR],0.72;P=0.12);然而,在复发后 12 个月以上的时间点,auto/allo 队列的总生存率更高(auto/auto 队列中死亡的 HR 为 1.55;P=0.005)。与生存改善相关的其他因素包括参加 HCT 的临床试验、男性和在 HCT 前诱导阶段使用新型药物。我们的研究结果表明,与接受 auto/auto HCT 的患者相比,接受 auto/allo HCT 的患者在复发后有更好的生存。这可能反映了对挽救治疗(如免疫调节剂)的反应更好,这得益于供体来源的免疫环境。用新的免疫疗法(如单克隆抗体、检查点抑制剂等)进一步增强 allo-HCT 后的免疫系统值得进一步研究。