Medical Research Education and Practice Association (MREP), Cairo, Egypt.
Al-Azhar Medical Students' Association (AMSA), Cairo, Egypt.
Support Care Cancer. 2018 Apr;26(4):1029-1038. doi: 10.1007/s00520-018-4060-1. Epub 2018 Feb 1.
Bone metastasis is reported to be associated with poor quality of life, and increased risk of hospitalization. We aim to synthesize evidence from published randomized controlled trials (RCTs) which compared the efficacy of denosumab versus bisphosphonates in patients with advanced cancers.
We searched for all published RCTs in the following electronic databases: PubMed, Scopus, Web of Science, and Cochrane Central. Retrieved records were screened for eligibility. Time-to-event data were pooled as hazard ratio (HR) using the generic inverse-variance method and dichotomous data were pooled as relative risk (RR) in a random-effect model. We used Review Manager 5.3 for windows.
Six unique RCTs with a total of 7722 patients were included. Overall effect estimates favored denosumab group in comparison to intravenous (IV) bisphosphonates in the following terms: time to first skeletal-related events (HR 0.92, 95% CI [0.86, 0.98], p = 0.01), time to subsequent skeletal-related event (RR 0.92, 95% CI [0.86, 0.99], p = 0.03), and radiation to bone (RR 0.81, 95% CI [0.71, 0.92], p = 0.02). Denosumab group was associated with increased risk of grade 3 or 4 hypocalcaemia (RR 1.99, 95% CI [1.11, 3.54], p = 0.02) and reduced risk of renal impairment or toxicity (RR 0.75, 95% CI [0.61, 0.91], p = 0.003) in comparison to IV bisphosphonates group. Pooled studies were homogenous.
Denosumab showed a favorable significant impact on delaying the time to first skeletal-related event and reducing the incidence of radiation to the bone event in comparison to bisphosphonates, with similar efficacy regarding overall survival and time to disease progression. Further large-scale and long-term studies are needed to clarify the long-term efficacy and safety of both regimens.
据报道,骨转移与生活质量下降和住院风险增加有关。我们旨在综合已发表的随机对照试验(RCT)的证据,比较地舒单抗与双膦酸盐在晚期癌症患者中的疗效。
我们在以下电子数据库中搜索了所有已发表的 RCT:PubMed、Scopus、Web of Science 和 Cochrane Central。筛选检索到的记录以确定其是否符合纳入标准。使用通用倒数方差法将生存时间数据汇总为风险比(HR),使用随机效应模型将二分类数据汇总为相对风险(RR)。我们使用 Review Manager 5.3 for windows 进行分析。
纳入了 6 项独特的 RCT,共有 7722 名患者。总体效应估计表明,与静脉内(IV)双膦酸盐相比,地舒单抗组在以下方面具有优势:首次骨骼相关事件的时间(HR 0.92,95%CI [0.86, 0.98],p=0.01)、随后骨骼相关事件的时间(RR 0.92,95%CI [0.86, 0.99],p=0.03)和骨放疗(RR 0.81,95%CI [0.71, 0.92],p=0.02)。与 IV 双膦酸盐组相比,地舒单抗组更易发生 3 级或 4 级低钙血症(RR 1.99,95%CI [1.11, 3.54],p=0.02),而肾功能损害或毒性(RR 0.75,95%CI [0.61, 0.91],p=0.003)的风险更低。汇总研究具有同质性。
与双膦酸盐相比,地舒单抗在延迟首次骨骼相关事件的时间和减少骨放疗事件的发生方面具有显著的有利影响,在总生存和疾病进展时间方面具有相似的疗效。需要进一步开展大规模和长期研究,以明确两种治疗方案的长期疗效和安全性。