Medicine A, Rabin Medical Center - Beilinson Hospital, 39 Jabotinski St., 4941492, Petach Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Osteoporos Int. 2021 Mar;32(3):413-424. doi: 10.1007/s00198-020-05704-6. Epub 2020 Nov 3.
The immunomodulatory effects of denosumab have raised concerns for risk of malignancy. This meta-analysis of 25 randomized controlled trials (21,523 patients) shows similar risk of malignancy between denosumab (60 mg every 6 months, up to 48 months) and any comparator. Post-marketing surveillance may detect rare or late-occurring drug effects. Possible increased risk of malignancy in patients treated with denosumab has been concerned due to inhibition of the immune modulator receptor activator of nuclear factor κ-Β ligand (RANKL). We aimed to assess the risk of malignancy associated with denosumab treatment. PubMed and Cochrane Central Register of Controlled Trials were searched up to May 27, 2019 to include all randomized controlled trials of denosumab (60 mg every 6 months) versus any comparator. Trials using higher drug doses for prevention of skeletal-related events were excluded. Data were independently extracted by two reviewers and analyzed using a fixed-effect model to pool risk ratios (RRs) with 95% confidence intervals (CI). Twenty-five trials (21,523 patients) were included. The risk of malignancy was similar between denosumab and other comparators (absolute risk difference 0%, RR 1.08 [95% CI, 0.93-1.24], I = 0%). Sensitivity analysis based on adequate allocation concealment showed similar results. The risk of malignancy did not differ between groups in any of the subgroup analyses, including stratification by race, individual comparators, indications for treatment, and longer drug exposure (≥ 24 months, 9 studies). The risk ratio of malignancy-related death was similar between groups. Early concerns about a potential increased risk of malignancy resulting from an immunomodulatory effect of denosumab are not supported by evidence from this meta-analysis of 25 RCTs with drug exposure of up to 48 months. Since RCTs with longer observation for safety outcomes are not expected, post-marketing surveillance will be the main means for detection of rare or late-occurring events.
地舒单抗的免疫调节作用引发了对恶性肿瘤风险的担忧。本项纳入 25 项随机对照试验(21523 例患者)的荟萃分析显示,地舒单抗(每 6 个月 60mg,最长 48 个月)与任何对照药物的恶性肿瘤风险相似。上市后监测可能会发现罕见或迟发的药物效应。由于抑制免疫调节剂核因子 κB 配体受体激活剂(RANKL),接受地舒单抗治疗的患者恶性肿瘤风险可能增加,这引起了人们的关注。我们旨在评估与地舒单抗治疗相关的恶性肿瘤风险。检索了截至 2019 年 5 月 27 日的 PubMed 和 Cochrane 对照试验中心注册库,以纳入所有地舒单抗(每 6 个月 60mg)与任何对照药物的随机对照试验。排除了用于预防骨骼相关事件的较高药物剂量的试验。由两位评审员独立提取数据,并使用固定效应模型分析以汇总风险比(RR)及其 95%置信区间(CI)。共纳入 25 项试验(21523 例患者)。地舒单抗与其他对照药物的恶性肿瘤风险相似(绝对风险差异 0%,RR 1.08[95%CI,0.93-1.24],I = 0%)。基于充分的分配隐匿的敏感性分析结果相似。在任何亚组分析中,包括按种族、个别对照药物、治疗指征和更长的药物暴露(≥24 个月,9 项研究)分层,两组间的恶性肿瘤风险均无差异。两组间恶性肿瘤相关死亡的风险比相似。这项纳入 25 项 RCT 的荟萃分析显示,长达 48 个月的药物暴露并未证实地舒单抗的免疫调节作用会导致恶性肿瘤风险增加的早期担忧。由于预计不会进行更长时间的安全性结果观察 RCT,上市后监测将是发现罕见或迟发事件的主要手段。