Efficacy and safety of ixazomib maintenance therapy for patients with multiple myeloma: a meta-analysis

被引:2
|
作者
Chen, Huixian [1 ]
Wang, Yongjing [1 ,3 ,4 ]
Shao, Chunchun [2 ]
Sun, Chenxi [1 ]
Zheng, Chengyun [1 ,3 ,4 ]
机构
[1] Shandong Univ, Hosp 2, Cheeloo Coll Med, Dept Hematol, Jinan, Peoples R China
[2] Shandong Univ, Hosp 2, Cheeloo Coll Med, Ctr Evidence Based Med,Inst Med Sci, Jinan, Peoples R China
[3] Shandong Univ Karolinska Inst Collaborat Lab Stem, Jinan, Peoples R China
[4] Shandong Univ, Inst Biotherapy Hematol Malignancies, Jinan, Peoples R China
关键词
Multiple myeloma; ixazomib; maintenance therapy; meta-analysis; STEM-CELL TRANSPLANTATION; MINIMAL RESIDUAL DISEASE; ORAL IXAZOMIB; SURVIVAL; RISK; LENALIDOMIDE; BORTEZOMIB;
D O I
10.1080/16078454.2021.2009648
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Multiple myeloma(MM) is a malignant plasma cell disease. Maintenance treatment is beneficial to prolong survival time in patients with MM. Ixazomib was approved for the treatment of relapsed or refractory MM in combination with lenalidomide and dexamethasone. Here, we carried out a meta-analysis to determine the efficacy and safety of ixazomib maintenance therapy. Methods Several databases were searched including PubMed, Web of Science, Embase, the Cochrane Library, etc. The last search dated back to July, 2020. Three clinical trials with a total of 1440 participants with newly diagnosed MM were included. Results and conclusion The pooled HR of progression-free survival (PFS) was 0.69 (95% CI = 0.59-0.79), which suggested ixazomib maintenance therapy could prolong PFS remarkably. In addition, ixazomib was effective in deepening remission (RR = 1.57, 95% CI = 1.26-1.96). But it could not significantly prolong PFS in cytogenetic high-risk patients (HR = 0.74, 95% CI = 0.47-1.00). In terms of adverse reactions, our analysis revealed higher incidences of grade 3-4 thrombocytopenia (RR = 7.47, 95% CI = 2.06-27.06), neuropathy (RR = 1.48, 95% CI = 1.14-1.92), grade 3-4 infections (RR = 1.77, 95% CI = 1.21-2.59) and gastrointestinal disorders (RR = 1.48, 95% CI = 1.32-1.66). There was no significant correlation between the use of ixazomib and grade 3-4 neutropenia (RR = 1.46, 95% CI = 0.77-2.78, p = 0.25) or the occurrence of new primary malignant tumor (RR = 0.88, 95% CI = 0.53-1.46, p = 0.62). Additionally, more RCTs are needed for better choice of treatment regimen.
引用
收藏
页码:1031 / 1039
页数:9
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