Guangxi Medical University, The Guangxi Zhuang Autonomous Region, Nanning, China.
Cancer Med. 2019 Sep;8(12):5414-5424. doi: 10.1002/cam4.2248. Epub 2019 Aug 8.
Melanoma is a potentially fatal malignancy with poor prognosis. Several recent studies have demonstrated that combination therapy of BRAF and MEK inhibition achieved better curative effect and appeared less toxic effects. We conducted a meta-analysis to evaluate the efficacy and safety between BRAF inhibition plus MEK inhibition combination therapy and BRAF inhibition monotherapy in melanoma patients.
We performed the search in PubMed, EMBASE, and the Cochrane Library from January 2010 to January 2019. Inclusion and exclusion of studies, assessment of quality, outcome measures, data extraction, and synthesis were independently accomplished by two reviewers. Revman 5.3 software was used for the meta-analysis.
Totally, seven randomized controlled trials involving 3146 patients met our inclusion criteria. Comparing the results of combination therapy and monotherapy, combination therapy significantly improved OS (RR = 1.13; 95% CI, 1.08, 1.19; P < 0.00001), ORR (RR = 1.36; 95% CI, 1.28, 1.45; P < 0.00001), PFS (RR = 0.57; 95% CI, 0.52, 0.63; P < 0.00001) and reduced deaths (RR = 0.78; 95% CI, 0.69, 0.88; P < 0.0001). Skin-related adverse events such as hyperkeratosis, cutaneous squamous-cell carcinoma were less compared with monotherapy. However, gastrointestinal events like nausea, diarrhea, and vomiting were at a higher frequency.
Doublet BRAF and MEK inhibition achieved better survival outcomes over single-agent BRAF inhibition and occurred less skin-related events, but gastrointestinal events were more in combination therapy.
黑色素瘤是一种预后不良的潜在致命恶性肿瘤。最近的几项研究表明,BRAF 和 MEK 抑制联合治疗的疗效更好,且毒副作用更小。我们进行了一项荟萃分析,以评估黑色素瘤患者中 BRAF 抑制加 MEK 抑制联合治疗与 BRAF 抑制单药治疗的疗效和安全性。
我们在 PubMed、EMBASE 和 Cochrane 图书馆中进行了搜索,时间范围为 2010 年 1 月至 2019 年 1 月。两名评审员独立完成了研究的纳入和排除、质量评估、结局指标、数据提取和综合分析。Revman 5.3 软件用于荟萃分析。
共有 7 项随机对照试验,涉及 3146 例患者,符合我们的纳入标准。与单药治疗相比,联合治疗显著改善了 OS(RR=1.13;95%CI,1.08,1.19;P<0.00001)、ORR(RR=1.36;95%CI,1.28,1.45;P<0.00001)、PFS(RR=0.57;95%CI,0.52,0.63;P<0.00001)和降低死亡率(RR=0.78;95%CI,0.69,0.88;P<0.0001)。与单药治疗相比,皮肤相关不良反应如角化过度、皮肤鳞状细胞癌的发生率较低。然而,胃肠道不良反应如恶心、腹泻和呕吐的发生率较高。
与单药 BRAF 抑制相比,双重 BRAF 和 MEK 抑制可获得更好的生存结果,且皮肤相关事件发生率较低,但联合治疗胃肠道事件发生率更高。