[Efficacy of a Daltuzumab-containing Regimen in Patients with mSMART High-Risk Multiple Myeloma].

Q4 Medicine
Zhen-Lun Qi, Ya-Qin Luo, Shu-Min Ding, Zhao-Xia Liu
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引用次数: 0

Abstract

Objective: To investigate the efficacy and safety of a treatment regimen based on daratumumab in patients with high-risk relapsed refractory multiple myeloma(MM) with mSMART 3.0 score.

Methods: Clinical data were collected from 16 patients with mSMART3.0 score high-risk relapsed refractory MM treated at the Affiliated Hospital of Shandong University of Traditional Chinese Medicine from May 2020 to May 2023, all of whom received daltezumab-based regimen (regimen drugs including dexamethasone, isazomib, bortezomib, lenalidomide). The efficacy and safety of the treatment were retrospectively analyzed.

Results: The median age of 16 patients was 63.5 (47-70) years old, including 10 cases of IgG type, 2 cases of IgA type, and 4 cases of light chain type. The curative efficacy was judged in all 16 patients, with an overall response rate of 93.75% (15/16), including 4 cases of strict complete remission (sCR), 1 case of complete remission (CR), 2 case of very good partial remission (VGPR), partial remission (PR) in 5 cases, and minor remission (MR) in 3 cases. The median follow-up time was 11(2-30) months, and the median progression-free survival and median overall survival were not achieved in 16 patients at the median follow-up period. The hematologic adverse effects of the treatment regimen using daratumumab-based were mainly neutropenia, and the non-hematologic adverse effects were mainly infusion-related adverse reactions and infections.

Conclusion: Daratumumab-based regimen for the treatment of relapsed refractory MM patients with high risk of mSMART3.0 score has better efficacy and safety.

[含达妥珠单抗方案对 mSMART 高危多发性骨髓瘤患者的疗效】。]
目的研究基于达拉单抗的治疗方案对mSMART3.0评分的高危复发难治性多发性骨髓瘤(MM)患者的疗效和安全性:收集山东中医药大学附属医院2020年5月至2023年5月收治的16例mSMART3.0评分高危复发难治性多发性骨髓瘤患者的临床资料,所有患者均接受达拉单抗为基础的治疗方案(方案药物包括地塞米松、伊沙佐米、硼替佐米、来那度胺)。对治疗的有效性和安全性进行了回顾性分析:16例患者的中位年龄为63.5(47-70)岁,其中IgG型10例,IgA型2例,轻链型4例。16 例患者均判定为治愈,总反应率为 93.75%(15/16),其中严格完全缓解(sCR)4 例,完全缓解(CR)1 例,很好部分缓解(VGPR)2 例,部分缓解(PR)5 例,轻微缓解(MR)3 例。中位随访时间为 11(2-30)个月,16 例患者在中位随访期间未达到中位无进展生存期和中位总生存期。基于达拉单抗的治疗方案的血液学不良反应主要是中性粒细胞减少,非血液学不良反应主要是输液相关不良反应和感染:结论:以达拉单抗为基础的方案治疗mSMART3.0评分高风险的复发难治性MM患者具有更好的疗效和安全性。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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