Early versus Deferred Treatment for Smoldering Multiple Myeloma: A Meta-Analysis of Randomized, Controlled Trials

被引:3
|
作者
Gao, Minjie [1 ]
Yang, Guang [1 ]
Tompkins, Van S. [2 ]
Gao, Lu [1 ]
Wu, Xiaosong [1 ]
Tao, Yi [1 ]
Hu, Xiaojing [1 ]
Hou, Jun [1 ]
Han, Ying [1 ]
Xu, Hongwei [3 ]
Zhan, Fenghuang [3 ]
Shi, Jumei [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Hematol, Shanghai 200092, Peoples R China
[2] Univ Iowa, Carver Coll Med, Dept Pathol, Iowa City, IA USA
[3] Univ Iowa, Carver Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
来源
PLOS ONE | 2014年 / 9卷 / 10期
基金
中国国家自然科学基金;
关键词
UNDETERMINED SIGNIFICANCE; MONOCLONAL GAMMOPATHY; STAGE-I; THERAPY; CHEMOTHERAPY; THALIDOMIDE; PROGRESSION; STRATEGIES; DIAGNOSIS; DISEASE;
D O I
10.1371/journal.pone.0109758
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: Whether patients with smoldering multiple myeloma (SMM) needed to receive early interventional treatment remains controversial. Herein, we conducted a meta-analysis comparing the efficacy and safety of early treatment over deferred treatment for patients with SMM. Methods: MEDLINE and Cochrane Library were searched to May 2014 for randomized controlled trials (RCTs) that assessed the effect of early treatment over deferred treatment. Primary outcome measure was mortality, and secondary outcome measures were progression, response rate, and adverse events. Results: Overall, 5 trials including 449 patients were identified. There was a markedly reduced risk of disease progression with early treatment (Odds Ratio [OR] = 0.13, 95% confidence interval [CI] = 0.07 to 0.24). There were no significant differences in mortality and response rate (OR = 0.85, 95%CI = 0.45 to 1.60, and OR = 0.63, 95%CI = 0.32 to 1.23, respectively). More patients in the early treatment arm experienced gastrointestinal toxicities (OR = 10.02, 95%CI = 4.32 to 23.23), constipation (OR = 8.58, 95%CI = 3.20 to 23.00) and fatigue or asthenia (OR = 2.72, 95%CI = 1.30 to 5.67). No significant differences were seen with the development of acute leukemia (OR = 2.80, 95%CI = 0.42 to 18.81), hematologic cancer (OR = 2.07, 95%CI = 0.43 to 10.01), second primary tumors (OR = 3.45, 95%CI = 0.81 to 14.68), nor vertebral compression (OR = 0.18, 95%CI = 0.02 to 1.59). Conclusions: Early treatment delayed disease progression but increased the risk of gastrointestinal toxicities, constipation and fatigue or asthenia. The differences on vertebral compression, acute leukemia, hematological cancer and second primary tumors were not statistically significant. Based on the current evidence, early treatment didn't significantly affect mortality and response rate. However, further much larger trials were needed to provide more evidence.
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页数:8
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