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达雷妥尤单抗治疗淀粉样变性患者结局的预测因素。

Predictive factors of outcomes in patients with AL amyloidosis treated with daratumumab.

机构信息

Amyloidosis Center, Boston University School of Medicine and Section of Hematology and Oncology, Boston Medical Center, Boston, Massachusetts, USA.

出版信息

Am J Hematol. 2022 Jan 1;97(1):79-89. doi: 10.1002/ajh.26399. Epub 2021 Nov 15.

Abstract

Daratumumab as a single agent (sDARA) or in combination with chemotherapies (cDARA) leads to impressive hematologic and organ responses in AL amyloidosis. However, predictive factors associated with outcomes, and optimal duration of therapy remain unclear. We analyzed 107 patients with AL amyloidosis treated with daratumumab between 2017 and 2020. The median overall survival (OS) was not reached while the median major organ deterioration progression free survival (MOD-PFS) was 36 months in the sDARA cohort and not reached in the cDARA cohort, respectively. Hematologic response > VGPR was achieved in 81% of patients receiving sDARA and 86% of patients treated with cDARA. Several predictive factors were identified on a univariate analysis, including NTproBNP >8500 pg/mL but only achievement of at least VGPR and presence of 1q21 gain were independently associated with MOD-PFS and OS on a multivariate analysis. Finally, patients receiving > 12 cycles had significantly longer MOD-PFS (30 vs.13 months; (p = .0018) and OS (NR vs. 15 months; p < .0001). NTproBNP > 8500 pg/mL, presence of 1q21 gain and shorter duration of therapy (≤ 12 cycles) are strong negative predictive factors for outcomes with daratumumab therapy in AL amyloidosis.

摘要

达雷妥尤单抗单药治疗(sDARA)或与化疗联合治疗(cDARA)可使 AL 淀粉样变性患者获得显著的血液学和器官反应。然而,与结局相关的预测因素以及最佳治疗持续时间仍不清楚。我们分析了 2017 年至 2020 年期间接受达雷妥尤单抗治疗的 107 例 AL 淀粉样变性患者。sDARA 组的中位总生存期(OS)未达到,而 cDARA 组的中位主要器官恶化无进展生存期(MOD-PFS)为 36 个月。sDARA 组有 81%的患者和 cDARA 组有 86%的患者达到了血液学缓解>非常好的部分缓解(VGPR)。单因素分析确定了几个预测因素,包括 NTproBNP>8500pg/mL,但仅至少达到 VGPR 和存在 1q21 增益与多因素分析中的 MOD-PFS 和 OS 相关。最后,接受>12 个周期治疗的患者具有显著更长的 MOD-PFS(30 个月比 13 个月;p=0.0018)和 OS(NR 比 15 个月;p<0.0001)。NTproBNP>8500pg/mL、存在 1q21 增益和较短的治疗持续时间(≤12 个周期)是 AL 淀粉样变性患者接受达雷妥尤单抗治疗结局的强烈负性预测因素。

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