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达雷妥尤单抗预处理对接受自体移植的多发性骨髓瘤患者的影响。

The impact of daratumumab pretreatment on multiple myeloma patients undergoing autologous transplantation.

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Kyoto Innovation Center for Next Generation Clinical Trials and iPS Cell Therapy, Kyoto University Hospital, Kyoto, Japan.

出版信息

Cancer Sci. 2024 Jul;115(7):2384-2395. doi: 10.1111/cas.16198. Epub 2024 May 16.

Abstract

The anti-CD38 antibody daratumumab (Dara) has been reported to improve the prognosis of multiple myeloma (MM) patients, but its use before autologous stem cell transplantation (ASCT) remains controversial. To clarify the prognostic impact of Dara before ASCT on MM, we performed a retrospective observational analysis. We analyzed 2626 patients who underwent ASCT between 2017 and 2020. In the comparison between patients not administered Dara (Dara- group) and those administered Dara (Dara+ group), the 1-year progression-free survival (PFS) rates were 87.4% and 77.3% and the 1-year overall survival (OS) rates were 96.7% and 90.0%, respectively. In multivariate analysis, age <65 years (p = 0.015), low international staging system (ISS) stage (p < 0.001), absence of unfavorable cytogenic abnormalities (p < 0.001), no Dara use before ASCT (p = 0.037), and good treatment response before ASCT (p < 0.001) were independently associated with superior PFS. In matched pair analysis, the PFS/OS of the Dara- group were also significantly superior. For MM patients who achieved complete or very good partial response (CR/VGPR) by Dara addition before ASCT, both PFS and OS significantly improved. However, in patients who did not achieve CR/VGPR before ASCT, the PFS/OS of the Dara+ group were significantly inferior to those of the Dara- group.

摘要

抗 CD38 抗体达雷妥尤单抗(Dara)已被报道可改善多发性骨髓瘤(MM)患者的预后,但在自体造血干细胞移植(ASCT)前使用仍存在争议。为了阐明 ASCT 前 Dara 对 MM 的预后影响,我们进行了一项回顾性观察性分析。我们分析了 2626 例在 2017 年至 2020 年间接受 ASCT 的患者。在未接受 Dara 治疗的患者(Dara-组)和接受 Dara 治疗的患者(Dara+组)之间,1 年无进展生存(PFS)率分别为 87.4%和 77.3%,1 年总生存(OS)率分别为 96.7%和 90.0%。多变量分析显示,年龄<65 岁(p=0.015)、低国际分期系统(ISS)分期(p<0.001)、无不良细胞遗传学异常(p<0.001)、ASCT 前未使用 Dara(p=0.037)和 ASCT 前治疗反应良好(p<0.001)与 PFS 改善独立相关。在匹配对分析中,Dara-组的 PFS/OS 也明显更好。对于 ASCT 前因 Dara 加用而达到完全或非常好的部分缓解(CR/VGPR)的 MM 患者,PFS 和 OS 均显著改善。然而,在 ASCT 前未达到 CR/VGPR 的患者中,Dara+组的 PFS/OS 明显劣于 Dara-组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b0/11247619/55386150d863/CAS-115-2384-g003.jpg

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