Weill Cornell Medical Center, New York, NY 10021, USA.
Bristol Myers Squibb, Princeton, NJ 08540, USA.
Future Oncol. 2021 Feb;17(6):689-699. doi: 10.2217/fon-2020-0643. Epub 2020 Oct 21.
To compare effectiveness of nivolumab + ipilimumab (NIVO + IPI) versus BRAF + MEK inhibitors (BRAFi + MEKi) in patients with -mutant advanced melanoma in the real-world setting. This study used the Flatiron Health electronic medical record database. After adjusting for differences in baseline characteristics, NIVO + IPI was associated with a 32% reduction in risk of death versus BRAFi + MEKi. At a mean follow-up of 15-16 months, 64% of NIVO + IPI patients and 43% of BRAFi + MEKi patients were alive; subsequent therapy was administered to 33 and 41% of patients, respectively. After first-line NIVO + IPI, 20% of patients died before subsequent therapy, whereas 32% died after first-line BRAFi + MEKi. In this real-world study, patients treated with first-line NIVO + IPI showed significant survival benefit versus those receiving first-line BRAFi + MEKi.
比较纳武利尤单抗+伊匹单抗(NIVO+IPI)与 BRAF+MEK 抑制剂(BRAFi+MEKi)在真实世界环境中治疗 - 突变型晚期黑色素瘤患者的疗效。本研究使用了 Flatiron Health 电子病历数据库。在调整了基线特征差异后,与 BRAFi+MEKi 相比,NIVO+IPI 降低了 32%的死亡风险。在平均 15-16 个月的随访中,NIVO+IPI 组 64%的患者和 BRAFi+MEKi 组 43%的患者存活;分别有 33%和 41%的患者接受了后续治疗。在一线治疗使用 NIVO+IPI 后,有 20%的患者在接受后续治疗前死亡,而一线使用 BRAFi+MEKi 后有 32%的患者死亡。在这项真实世界研究中,与一线接受 BRAFi+MEKi 治疗的患者相比,一线接受 NIVO+IPI 治疗的患者显示出显著的生存获益。