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首页> 外文期刊>BMC Cancer >Comparative efficacy and safety of adjuvant nivolumab versus other treatments in adults with resected melanoma: a systematic literature review and network meta-analysis
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Comparative efficacy and safety of adjuvant nivolumab versus other treatments in adults with resected melanoma: a systematic literature review and network meta-analysis

机译:佐剂Nivolumab对成年人的比较疗效和安全性与切割黑素瘤的其他治疗方法:系统文献综述和网络元分析

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Abstract Background Immune checkpoint inhibitors and targeted therapies are approved for adjuvant treatment of patients with resected melanoma; however, they have not been compared in randomized controlled trials (RCTs). We compared the efficacy and safety of adjuvant nivolumab with other approved treatments using available evidence from RCTs in a Bayesian network meta-analysis (NMA). Methods A systematic literature review was conducted through May 2019 to identify relevant RCTs evaluating approved adjuvant treatments. Outcomes of interest included recurrence-free survival (RFS)/disease-free survival (DFS), distant metastasis-free survival (DMFS), all-cause grade 3/4 adverse events (AEs), discontinuations, and discontinuations due to AEs. Time-to-event outcomes (RFS/DFS and DMFS) were analyzed both assuming that hazard ratios (HRs) are constant over time and that they vary. Results Of 26 identified RCTs, 19 were included in the NMA following a feasibility assessment. Based on HRs for RFS/DFS, the risk of recurrence with nivolumab was similar to that of pembrolizumab and lower than that of ipilimumab 3?mg/kg, ipilimumab 10?mg/kg, or interferon. Risk of recurrence with nivolumab was similar to that of dabrafenib plus trametinib at 12?months, however, was lower beyond 12?months (HR [95% credible interval] at 24?months, 0.46 [0.27–0.78]; at 36?months, 0.28 [0.14–0.59]). Based on HRs for DMFS, the risk of developing distant metastases was lower with nivolumab than with ipilimumab 10?mg/kg or interferon and was similar to dabrafenib plus trametinib. Conclusion Adjuvant therapy with nivolumab provides an effective treatment option with a promising risk–benefit profile.
机译:摘要背景免疫检查点抑制剂和靶向疗法被批准用于切除黑素瘤患者的辅助治疗;但是,它们尚未在随机对照试验(RCT)中进行比较。我们将佐剂Nivolumab与其他经批准的治疗的疗效和安全性进行了比较了使用来自RCT在贝叶斯网络Meta-Analysis(NMA)中的可用证据进行的现有证据。方法通过2019年5月进行系统文献综述,以确定评估批准的佐剂治疗的相关RCT。感兴趣的结果包括无复发的存活(RFS)/无病生存(DFS),远处转移存活(DMF),由于AES而导致的3/4不良事件(AES),中断和中断。假设危险比(HRS)随着时间的推移,危险比率(HRS)恒定,分析了事件时间结果(RFS / DFS和DMFS)。在可行性评估之后,26个鉴定的RCT,19件包含在NMA中。基于RFS / DF的HRS,与幼肠病的复发风险类似于Pembrolizumab的风险,低于Ipilimalab 3?Mg / kg,Ipilimalab 10?mg / kg或干扰素。与幼虫动物的复发风险类似于Dabrafenib Plus Trametinib在12?几个月的危机中的危险与24个月(HR [95%可靠的间隔] 24个月,0.46 [0.27-0.78];在36?月份,0.28 [0.14-0.59])。基于HRS对于DMFS,患远处转移的风险与Nivolumab较低,而不是Ipilimalab 10?Mg / kg或干扰素,并且类似于Dabrafenib Plus Trametinib。结论Nivolumab的佐剂治疗提供了有效的风险福利概况的有效治疗选择。

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