Pasvolsky Oren, Abid Muhammad Bilal, Milton Denái R, Tanner Mark R, Bashir Qaiser, Srour Samer, Saini Neeraj, Jatoi Asiya, Khan Hina N, Lin Paul, Ramdial Jeremy, Nieto Yago, Tang Guilin, Siddiqui Umer, Aljawai Yosra, Kebriaei Partow, Lee Hans C, Patel Krina K, Gaballa Mahmoud R, Thomas Sheeba K, Orlowski Robert Z, Champlin Richard E, Shpall Elizabeth J, Qazilbash Muzaffar H
Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Br J Haematol. 2025 Jun;206(6):1730-1736. doi: 10.1111/bjh.20062. Epub 2025 Mar 30.
There are scarce data in the literature focusing on newly diagnosed multiple myeloma (NDMM) patients who undergo autologous haematopoietic cell transplantation (autoHCT) after achieving suboptimal response to induction. To address this, we performed a retrospective, single-centre analysis of patients with NDMM who underwent upfront autoHCT between 2005 and 2021 with a pretransplant response of less than very good partial response (<VGPR). Primary outcomes were progression-free survival (PFS) and overall survival (OS). 1109 patients were included in our analysis. Median PFS and OS for the entire cohort were 38.6 (95% confidence interval [CI], 35.9-41.9) months and 103.8 (95% CI, 96.4-113.2) months, respectively. Patients with high-risk cytogenetic abnormalities (HRCA) had a median PFS and OS of 24.8 months and 69.9 months respectively. In multivariable analysis, the use of post-transplant maintenance (hazard ratio [HR] 0.75, p = 0.001 and HR 0.75, p = 0.008) and achieving complete response (CR) at best post-transplant response (HR 0.60, p < 0.001 and HR 0.51, p < 0.001) were associated with superior PFS and OS respectively. In conclusion, NDMM patients who received upfront autoHCT with a pretransplant response of
文献中关于新诊断的多发性骨髓瘤(NDMM)患者在诱导治疗反应欠佳后接受自体造血细胞移植(autoHCT)的数据很少。为了解决这个问题,我们对2005年至2021年间接受前期autoHCT且移植前反应小于非常好的部分缓解(<VGPR)的NDMM患者进行了一项回顾性单中心分析。主要结局是无进展生存期(PFS)和总生存期(OS)。我们的分析纳入了1109例患者。整个队列的中位PFS和OS分别为38.6(95%置信区间[CI],35.9 - 41.9)个月和103.8(95%CI,96.4 - 113.2)个月。具有高危细胞遗传学异常(HRCA)的患者中位PFS和OS分别为24.8个月和69.9个月。在多变量分析中,移植后维持治疗的使用(风险比[HR] 0.75,p = 0.001和HR 0.75,p = 0.008)以及在移植后最佳反应时达到完全缓解(CR)(HR 0.60,p < 0.001和HR 0.51,p < 0.001)分别与更好的PFS和OS相关。总之,移植前反应为<VGPR的接受前期autoHCT的NDMM患者中位PFS大于3年,中位OS大于8年。移植后维持治疗进一步改善了生存结局。