Wang Xiaoxue, Yan Xiaojing, Li Yan
Department of Hematology, The First Hospital of China Medical University Shenyang 110001, China.
Int J Clin Exp Med. 2015 May 15;8(5):6743-54. eCollection 2015.
The objective of this meta-analysis was to determine the effectiveness and safety of bisphosphonates (BPs) for patients with multiple myeloma (MM).
The study included patients with MM, who were randomly allocated to receive either BPs or control. PubMed/Medline, Embase, the Cochrane Database of Systematic Reviews (CDSR), and the Cochrane Central Register of Controlled Trials were searched up to January 2014, and only published trials were included in the analysis. There was no language restriction. The results were analyzed using RevMan 5.2 software, which was provided by Cochrane Collaboration.
Six randomized controlled trials (RCTs) covering 1951 patients with MM were included in the analysis. The clodronate subgroup showed superior progression-free survival compared to the other groups. The pooled hazard ratio (HR) was 0.57 [95% confidence interval (CI) 0.33-0.99, P = 0.04]. Regarding overall survival (OS), only zoledronic acid showed a clear advantage (HR = 0.51, 95% CI 0.33-0.77, P = 0.002) All BPs were effective at reducing skeletal-related events (SREs). The pooled risk ratios for the outcome of SREs were 0.72 (95% CI: 0.62-0.84, P < 0.0001) for the clodronate subgroup, 0.66 (95% CI: 0.48-0.91, P = 0.007) for the pamidronate subgroup, and 0.65 (95% CI: 0.46-0.91, P = 0.01) for the zoledronic acid subgroup. Several adverse events (AEs) were mentioned in the included RCTs; however, the pooled results showed no statistically significant differences between the BP groups and the control.
The present meta-analysis demonstrated that zoledronic acid may improve the OS of patients with MM. All BPs markedly decreased SREs and were tolerated well.
本荟萃分析的目的是确定双膦酸盐(BPs)对多发性骨髓瘤(MM)患者的有效性和安全性。
该研究纳入了MM患者,这些患者被随机分配接受BPs或对照治疗。检索了截至2014年1月的PubMed/Medline、Embase、Cochrane系统评价数据库(CDSR)和Cochrane对照试验中央注册库,分析仅纳入已发表的试验。无语言限制。使用Cochrane协作网提供的RevMan 5.2软件对结果进行分析。
分析纳入了6项随机对照试验(RCT),共1951例MM患者。氯膦酸盐亚组的无进展生存期优于其他组。合并风险比(HR)为0.57 [95%置信区间(CI)0.33 - 0.99,P = 0.04]。关于总生存期(OS),仅唑来膦酸显示出明显优势(HR = 0.51,95% CI 0.33 - 0.77,P = 0.002)。所有BPs在降低骨相关事件(SREs)方面均有效。氯膦酸盐亚组SREs结局的合并风险比为0.72(95% CI:0.62 - 0.84,P < 0.0001),帕米膦酸亚组为0.66(95% CI:0.48 - 0.91,P = 0.007),唑来膦酸亚组为0.65(95% CI:0.46 - 0.91,P = 0.01)。纳入的RCT中提到了几种不良事件(AE);然而,合并结果显示BP组与对照组之间无统计学显著差异。
本荟萃分析表明唑来膦酸可能改善MM患者的OS。所有BPs均显著降低SREs且耐受性良好