Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petah-Tikva, Israel.
Bone Marrow Transplant. 2021 Apr;56(4):928-935. doi: 10.1038/s41409-020-01136-2. Epub 2020 Nov 18.
The goal of therapy in AL amyloidosis is to inhibit further production of the amyloidogenic light chains, thereby allowing organ recovery and improving survival. We aimed to assess the impact of depth of hematologic response prior to ASCT on survival. We conducted a retrospective study of 128 newly diagnosed AL amyloidosis patients who received induction prior to ASCT between January 2007 and August 2017 at Mayo Clinic. The overall response rate to induction was 86% (CR 18%, VGPR 31% and PR 38%). With a median follow up of 52 months, the median PFS and OS was 48.5 months and not reached, respectively. Response depth to induction therapy was associated with improved PFS and OS. The median PFS was not reached for patients achieving ≥VGPR prior to ASCT and 34.1 months for patients achieving PR or less (P = 0.0009). The median OS was longer in patients with deeper responses (not reached for ≥VGPR vs. 128 months for PR or less (P = 0.02)). On multivariable analysis, independent predictors of OS were melphalan conditioning dose (RR = 0.42; P = 0.036) and depth of response prior to transplant (RR 0.37; P = 0.0295). Hematologic response prior to transplant predicts improved post transplant outcomes in AL amyloidosis.
淀粉样变多发性骨髓瘤的治疗目标是抑制淀粉样生成轻链的进一步产生,从而使器官恢复并提高生存率。我们旨在评估 ASCT 前血液学反应的深度对生存的影响。我们对 2007 年 1 月至 2017 年 8 月期间在梅奥诊所接受 ASCT 前诱导治疗的 128 例新诊断的淀粉样变性多发性骨髓瘤患者进行了回顾性研究。诱导治疗的总反应率为 86%(完全缓解 18%,非常好的部分缓解 31%,部分缓解 38%)。中位随访 52 个月时,中位无进展生存期和总生存期分别为 48.5 个月和未达到。诱导治疗反应深度与无进展生存期和总生存期改善相关。ASCT 前达到≥非常好的部分缓解的患者中位无进展生存期未达到,而达到部分缓解或更低缓解的患者中位无进展生存期为 34.1 个月(P=0.0009)。反应更深的患者中位总生存期更长(达到≥非常好的部分缓解的患者未达到,而达到部分缓解或更低缓解的患者为 128 个月(P=0.02))。多变量分析显示,总生存期的独立预测因素为马法兰预处理剂量(RR=0.42;P=0.036)和移植前反应深度(RR 0.37;P=0.0295)。移植前血液学反应可预测淀粉样变性多发性骨髓瘤患者移植后的预后改善。