Department of Dermatology and Allergy, University Hospital, LMU Munich, Frauenlobstr. 9-11, 80337 Munich, Germany.
Department of Dermatology and Allergy, University Hospital, LMU Munich, Frauenlobstr. 9-11, 80337 Munich, Germany.
Eur J Cancer. 2018 Nov;103:41-51. doi: 10.1016/j.ejca.2018.08.005. Epub 2018 Sep 8.
BRAF and MEK inhibitors have demonstrated significant survival benefits for patients with cutaneous melanoma. However, their use for uveal melanoma (UM) is less established. The aim of this systematic review was to summarise the current evidence on the efficacy and safety of MEK inhibitors in metastatic UM.
We performed a systematic literature search in MEDLINE, Embase and the Cochrane Library CENTRAL from 1946 through 17 April 2018. Abstracts of oncologic conferences, trial registers and reference lists were handsearched for relevant publications. The risk of bias was assessed with the Cochrane Risk of Bias Tool.
Of 590 records identified, six studies met the eligibility criteria and were included in the qualitative synthesis. Data were available for selumetinib ± dacarbazine (n = 3), trametinib ± AKT inhibitor (n = 2) and binimetinib plus sotrastaurin (n = 1) from three open-label phase II, two open-label phase I and one placebo-controlled phase III trial. The overall response rate was available in five studies and ranged from 0 to 14% with an average of 2.5%. The median progression-free survival ranged from 3.1 weeks to 16 weeks. Data on overall survival and 1-year survival rates were not consistently reported. Severe treatment-related adverse events were observed most commonly for the combination use of selumetinib plus dacarbazine (62%) and binimetinib plus sotrastaurin (75%).
UM is little responsive to MEK inhibition, regardless of the inhibiting agent and combination partner. Our results do not support the use of MEK inhibitors in UM. Novel treatment options are urgently needed in this patient population.
BRAF 和 MEK 抑制剂已被证实可显著改善皮肤黑色素瘤患者的生存获益。然而,其在葡萄膜黑色素瘤(UM)中的应用尚不确定。本系统评价的目的是总结目前关于 MEK 抑制剂在转移性 UM 中的疗效和安全性的证据。
我们在 MEDLINE、Embase 和 Cochrane Library CENTRAL 中进行了系统的文献检索,检索时间从 1946 年到 2018 年 4 月 17 日。检索肿瘤学会议摘要、试验登记册和参考文献列表,以查找相关出版物。使用 Cochrane 偏倚风险工具评估偏倚风险。
在 590 篇记录中,有 6 项研究符合纳入标准,并进行了定性综合分析。有 3 项研究纳入了 selumetinib ± 达卡巴嗪的数据(n=3),2 项研究纳入了 trametinib ± AKT 抑制剂的数据(n=2),1 项研究纳入了 binimetinib 联合 sotrastaurin的数据(n=1),这些数据分别来自 3 项开放标签 II 期、2 项开放标签 I 期和 1 项安慰剂对照 III 期试验。有 5 项研究报告了总缓解率,范围为 0 至 14%,平均为 2.5%。中位无进展生存期从 3.1 周到 16 周不等。总生存数据和 1 年生存率数据未得到一致报告。最常见的严重治疗相关不良事件发生在 selumetinib 联合达卡巴嗪(62%)和 binimetinib 联合 sotrastaurin(75%)的联合用药中。
UM 对 MEK 抑制反应不佳,与抑制剂和联合用药伙伴无关。我们的结果不支持在 UM 中使用 MEK 抑制剂。在该患者人群中迫切需要新的治疗选择。