Yun Seongseok, Vincelette Nicole D, Green Myke R, Wahner Hendrickson Andrea E, Abraham Ivo
Department of Medicine, University of Arizona, Tucson, Arizona, 85721.
Hematology and Oncology, University of Arizona, Tucson, Arizona, 85721.
Cancer Med. 2016 Jul;5(7):1481-91. doi: 10.1002/cam4.732. Epub 2016 May 11.
Anti-cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) and anti-programmed cell death-1 (PD-1) inhibitors have been shown to significantly improve survival in patients with metastatic cutaneous melanoma. However, there was some heterogeneity as well as some variation in the degree of benefit across studies. We reviewed randomized trials and performed a meta-analysis to determine the efficacy and safety of immune checkpoint inhibitors in comparison with conventional regimens. Eligible studies were limited to randomized controlled trials comparing anti-CTLA-4 or anti-PD-1 inhibitors to chemotherapy or vaccination treatment in adult patients with unresectable cutaneous metastatic melanoma. Progression-free survival (PFS) rate at 6 months was 28.5% versus 17.7% (RR: 0.84, 95% CI: 0.76-0.93), overall survival (OS) rate at 1 year was 51.2% versus 38.8% (RR: 0.72, 95% CI: 0.59-0.88), and overall response rate (ORR) at 6 months was 29.6% versus 17.7% (RR: 0.85, 95% CI: 0.76-0.95) favoring immune check point inhibitors over chemotherapies or vaccination. Immune check point inhibitors were associated with more frequent immune-related adverse events at 13.7% versus 2.4% of treated patients (RR: 6.74, 95% CI: 4.65-9.75). Subgroup analyses demonstrated significant PFS (RR: 0.92 vs. 0.74, P < 0.00001) and ORR (RR: 0.95 vs. 0.76, P = 0.0004) improvement with anti-PD-1 treatment compared to anti-CTLA-4 when each of them was compared to control treatments. Collectively, these results demonstrate that immune checkpoint inhibitors have superior outcomes compared to conventional chemotherapies or vaccination, and support the results of recent randomized trials that showed superior outcomes with anti-PD-1 agents over ipilimumab in unresectable metastatic cutaneous melanoma patients.
抗细胞毒性T淋巴细胞相关抗原4(CTLA-4)和抗程序性细胞死亡蛋白1(PD-1)抑制剂已被证明能显著提高转移性皮肤黑色素瘤患者的生存率。然而,不同研究之间存在一定的异质性,获益程度也有所不同。我们回顾了随机试验并进行了荟萃分析,以确定免疫检查点抑制剂与传统治疗方案相比的疗效和安全性。符合条件的研究仅限于将抗CTLA-4或抗PD-1抑制剂与化疗或疫苗治疗进行比较的随机对照试验,受试对象为患有不可切除皮肤转移性黑色素瘤的成年患者。6个月时的无进展生存率(PFS)分别为28.5%和17.7%(风险比:0.84,95%置信区间:0.76 - 0.93),1年时的总生存率(OS)分别为51.2%和38.8%(风险比:0.72,95%置信区间:0.59 - 0.88),6个月时的总缓解率(ORR)分别为29.6%和17.7%(风险比:0.85,95%置信区间:0.76 - 0.95),表明免疫检查点抑制剂优于化疗或疫苗治疗。免疫检查点抑制剂与更频繁的免疫相关不良事件相关,接受治疗的患者中发生率分别为13.7%和2.4%(风险比:6.74,95%置信区间:4.65 - 9.75)。亚组分析显示,与对照组治疗相比,抗PD-1治疗在PFS(风险比:0.92对0.74,P < 0.00001)和ORR(风险比:0.95对0.76,P = 0.0004)方面均有显著改善,且抗PD-1治疗与抗CTLA-4治疗相比也是如此。总体而言,这些结果表明,与传统化疗或疫苗治疗相比,免疫检查点抑制剂具有更好的疗效,支持了近期随机试验的结果,即在不可切除的转移性皮肤黑色素瘤患者中,抗PD-1药物比伊匹单抗具有更好的疗效。