Health Services Research Unit, University of Aberdeen, Aberdeen, UK.
Eur J Cancer. 2013 Jan;49(2):416-30. doi: 10.1016/j.ejca.2012.07.016. Epub 2012 Aug 18.
To evaluate the evidence for denosumab for the treatment of bone metastases secondary to solid tumours and, using a network meta-analysis, indirectly compare denosumab with bisphosphonates and best supportive care.
MEDLINE (1948 to April 2011), EMBASE (1980 to March 2011), Cochrane Library (all sections) (issue 1, 2011) and Web of Science with Conference Proceedings (1970 to May 2011) and additional meeting abstracts (2010 and 2011) were searched. STUDY ELIGIBILITY, PARTICIPANTS AND INTERVENTIONS: Only randomised controlled trials assessing denosumab, bisphosphonates or best supportive care in patients with bone metastases from any solid tumour were included.
Direct evidence comparing denosumab and zoledronic acid was assessed for breast cancer, prostate cancer and other solid tumours. Denosumab was compared with pamidronate and best supportive care through a network meta-analysis for each tumour type. The primary outcomes were time to first skeletal related event (SRE) and time to first and subsequent SRE. Secondary outcomes were skeletal morbidity rate, pain, quality of life (QoL) and overall survival.
Denosumab was found to be more effective in delaying the time to first SRE and reducing the risk of first and subsequent SRE compared to zoledronic acid, placebo and pamidronate. In breast and prostate cancer, denosumab was effective in reducing skeletal morbidity rate compared with placebo. The lack of published data on pain and QoL meant that firm conclusions could not be made. Denosumab did not appear to have an affect on overall survival.
Network meta-analyses are subject to uncertainties and potential biases.
Denosumab is effective in preventing SRE, but the effect on pain and QoL is unclear.
评估地舒单抗治疗实体瘤所致骨转移的疗效,并通过网络荟萃分析间接比较地舒单抗与双膦酸盐和最佳支持治疗的疗效。
检索 MEDLINE(1948 年至 2011 年 4 月)、EMBASE(1980 年至 2011 年 3 月)、Cochrane 图书馆(所有部分)(2011 年第 1 期)和 Web of Science with Conference Proceedings(1970 年至 2011 年 5 月)以及其他会议摘要(2010 年和 2011 年)。
研究入选标准、参与者和干预措施:仅纳入评估地舒单抗、双膦酸盐或最佳支持治疗用于治疗任何实体瘤骨转移患者的随机对照试验。
评估了地舒单抗与唑来膦酸治疗乳腺癌、前列腺癌和其他实体瘤的直接证据。通过网络荟萃分析,比较了地舒单抗与帕米膦酸和最佳支持治疗在每种肿瘤类型中的疗效。主要结局指标为首次骨骼相关事件(SRE)时间和首次及随后 SRE 时间。次要结局指标为骨骼发病率、疼痛、生活质量(QoL)和总生存期。
与唑来膦酸、安慰剂和帕米膦酸相比,地舒单抗能更有效地延迟首次 SRE 时间,并降低首次及随后 SRE 的风险。在乳腺癌和前列腺癌中,与安慰剂相比,地舒单抗能有效降低骨骼发病率。由于缺乏关于疼痛和 QoL 的已发表数据,因此无法得出确切结论。地舒单抗似乎对总生存期没有影响。
网络荟萃分析存在不确定性和潜在偏倚。
地舒单抗能有效预防 SRE,但对疼痛和 QoL 的影响尚不清楚。