[Efficacy and Safety of Ixazomib Combined with Thalidomide and Dexamethasone in Treatment of Multiple Myeloma].

Xiang-Mei Yao, Zhi-Xiang Lu, Jian-Hua Rao, Xiao-Li Gao, Qi Wang, Hai-Tao He
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Abstract

Objective: To investigate the efficacy and safety of ixazomib combined with thalidomide and dexamethasone in the treatment of multiple myeloma (MM).

Methods: The clinical data of 60 MM patients admitted to our center from January 2019 to June 2022 were analyzed retrospectively, including 43 newly diagnosed patients and 17 patients with recurrence and progression. All patients were treated with ixazomib combined with thalidomide and dexamethasone, and completed 2 to 7 treatment cycles.

Results: The overall response rate (ORR) of all patients was 98.3%. Among them, 53 patients completed 4 treatment cycles, and the ORR was 86.8%. Seventeen patients completed the whole treatment cycle, with curative effect reaching 88.2% achieving very good partial response and above, and 52.9% achieving complete response and above. Albumin and β2-microglobulin of all patients had been improved rapidly after treatment. The deadline was August 31, 2022. The median follow-up time was 14(3-24) months, and overall survival (OS) rate was 86.67%. The OS rate of patients with recurrence and progression was significantly lower than that of newly diagnosed patients (P < 0.05). The most common adverse reaction of hematology was lymphopenia (53.3%), followed by anemia (33.3%). The most common non-hematological adverse reaction was fatigue (68.33%), followed by peripheral neuropathy (31.67%).

Conclusion: Ixazomib combined with thalidomide and dexamethasone is effective in the treatment of MM, with good short-term efficacy, survival and safety. However, its long-term efficacy needs further observation.

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[伊沙佐米联合沙利度胺和地塞米松治疗多发性骨髓瘤的疗效和安全性]。
目的研究伊沙佐米联合沙利度胺和地塞米松治疗多发性骨髓瘤(MM)的疗效和安全性:回顾性分析我中心2019年1月至2022年6月收治的60例MM患者的临床资料,其中包括43例新诊断患者和17例复发及病情进展患者。所有患者均接受了伊沙佐米联合沙利度胺和地塞米松治疗,并完成了2至7个治疗周期:所有患者的总反应率(ORR)为98.3%。结果:所有患者的总反应率(ORR)为 98.3%,其中 53 例患者完成了 4 个治疗周期,ORR 为 86.8%。17例患者完成了整个治疗周期,疗效达到88.2%的患者获得了很好的部分反应及以上,52.9%的患者获得了完全反应及以上。所有患者的白蛋白和β2-微球蛋白在治疗后都得到了迅速改善。截止日期为 2022 年 8 月 31 日。中位随访时间为 14(3-24)个月,总生存率(OS)为 86.67%。复发和病情进展患者的 OS 率明显低于新诊断患者(P < 0.05)。最常见的血液学不良反应是淋巴细胞减少(53.3%),其次是贫血(33.3%)。最常见的非血液学不良反应是疲劳(68.33%),其次是周围神经病变(31.67%):结论:伊沙佐米联合沙利度胺和地塞米松治疗MM有效,具有良好的短期疗效、生存率和安全性。结论:伊沙佐米联合沙利度胺和地塞米松治疗 MM 有良好的短期疗效、生存率和安全性,但其长期疗效还需进一步观察。
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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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