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基于血清游离轻链水平的非固定周期达雷妥尤单抗治疗轻链型淀粉样变性患者的策略

Serum free light chain level-based and non-fixed cycle daratumumab treatment strategy for patients with light chain amyloidosis.

作者信息

Li Zhen, Guo Jinzhou, Chen Wencui, Zhao Liang, Ren Guisheng, Huang Xianghua

机构信息

National Clinical Research Center for Kidney Diseases, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

出版信息

Ann Med. 2025 Dec;57(1):2442075. doi: 10.1080/07853890.2024.2442075. Epub 2024 Dec 19.

Abstract

BACKGROUND

In recent years, daratumumab (DARA) has gained widespread use in the treatment of systemic light chain (AL) amyloidosis. In this study, we assessed the efficacy and safety of a DARA treatment strategy based on serum free light chain (sFLC) levels and non-fixed cycles.

METHODS

The study included 123 patients with Al amyloidosis who received DARA at our center between July 2020 and September 2023. All patients received the standard DARA treatment (16 mg/kg weekly for four weeks) during the first course. Subsequent treatments were adjusted based on sFLC levels and the physician's judgment.

RESULTS

The results demonstrated an impressive overall hematologic response rate (ORR) of 94.3%, with a hematologic very good partial response (VGPR) and complete response (CR) rate of 84.5%. Median time to best hematologic response was 1 months. Cardiac and renal response rates were 39.3% and 60.3%, respectively. Thirty patients experienced grade 1/2 infusion-related reactions after the first infusion. The rate of grade 3/4 adverse events was 21%. The most common adverse events of grade 3 or 4 were pulmonary infection (6.5%), neutropenia and lymphocytopenia (5.7%), elevated transaminases (1.6%), acute kidney injury (1.6%). After a median follow-up of 13 months (range 1-38), The 1-year OS and PFS estimates were 96.5% and 84.4%, respectively.

CONCLUSION

These findings indicate that the sFLC levels based and non-fixed cycle DARA strategy is an efficacious and safe treatment strategy in both newly diagnosed and relapsed/refractory AL amyloidosis.

摘要

背景

近年来,达雷妥尤单抗(DARA)在系统性轻链(AL)淀粉样变性的治疗中得到广泛应用。在本研究中,我们评估了基于血清游离轻链(sFLC)水平和非固定周期的DARA治疗策略的疗效和安全性。

方法

本研究纳入了2020年7月至2023年9月期间在我们中心接受DARA治疗的123例AL淀粉样变性患者。所有患者在第一个疗程中接受标准DARA治疗(每周16mg/kg,共四周)。后续治疗根据sFLC水平和医生的判断进行调整。

结果

结果显示总体血液学缓解率(ORR)高达94.3%,血液学非常好的部分缓解(VGPR)和完全缓解(CR)率为84.5%。达到最佳血液学缓解的中位时间为1个月。心脏和肾脏缓解率分别为39.3%和60.3%。30例患者在首次输注后出现1/2级输注相关反应。3/4级不良事件发生率为21%。最常见的3或4级不良事件为肺部感染(6.5%)、中性粒细胞减少和淋巴细胞减少(5.7%)、转氨酶升高(1.6%)、急性肾损伤(1.6%)。中位随访13个月(范围1-38个月)后,1年总生存率(OS)和无进展生存率(PFS)估计分别为96.5%和84.4%。

结论

这些发现表明,基于sFLC水平和非固定周期的DARA策略在新诊断和复发/难治性AL淀粉样变性中是一种有效且安全的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4983/11660285/b1b121f5fb64/IANN_A_2442075_F0001_C.jpg

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