Thakker Sach, Belzberg Micah, Jang Sekwon, Al-Mondhiry Jafar
Georgetown University School of Medicine, Washington, DC, United States.
Department of Dermatology, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Oncologist. 2024 Dec 6;29(12):e1783-e1785. doi: 10.1093/oncolo/oyae248.
The use of programmed death-1 (PD-1) inhibitors has been a pivotal advancement in treating advanced melanoma, yet their efficacy is limited. The approval of relatlimab (RELA), a lymphocyte activation gene 3 protein (LAG-3) antibody, in combination with nivolumab (NIVO), a PD-1 inhibitor, marked a significant stride toward enhancing treatment efficacy for metastatic and unresectable stage 3 and 4 melanoma. This combination has been shown to synergistically improve antitumor activity and effector T-cell activity in the tumor microenvironment, despite limited data on real-world outcomes. Our retrospective review at a tertiary cancer center of patients with stage 3 and 4 melanoma treated with NIVO-RELA revealed an overall response rate (ORR) of 39%, with notable improvements in median PFS and ORR, especially in first-line treated patients. Our study highlights the superior efficacy of NIVO-RELA over previous reports, demonstrating its significant potential in the treatment landscape of advanced melanoma.
程序性死亡-1(PD-1)抑制剂的使用是治疗晚期黑色素瘤的一项关键进展,但其疗效有限。淋巴细胞激活基因3蛋白(LAG-3)抗体relatlimab(RELA)与PD-1抑制剂纳武单抗(NIVO)联合使用获得批准,标志着在提高转移性和不可切除的3期和4期黑色素瘤治疗效果方面迈出了重要一步。尽管关于真实世界疗效的数据有限,但这种联合用药已被证明可协同改善肿瘤微环境中的抗肿瘤活性和效应T细胞活性。我们在一家三级癌症中心对接受NIVO-RELA治疗的3期和4期黑色素瘤患者进行的回顾性研究显示,总缓解率(ORR)为39%,中位无进展生存期和ORR有显著改善,尤其是在一线治疗的患者中。我们的研究突出了NIVO-RELA相对于先前报告的卓越疗效,证明了其在晚期黑色素瘤治疗领域的巨大潜力。