First Department of Medical Oncology, Metropolitan Hospital, N. Faliro.
First Department of Medicine, Laiko General Hospital, National and Kapodistrian University of Athens School of Medicine.
Melanoma Res. 2019 Aug;29(4):428-434. doi: 10.1097/CMR.0000000000000562.
This retrospective cohort study assessed the prognostic significance of distant metastasis-free interval (DMFI) in patients with relapsed BRAF-mutant melanoma treated with BRAF with or without MEK inhibitors (BRAFi ± MEKi). Patients with a DMFI of up to 24 months were compared with those with DMFI of more than 24 months, with regard to their postrelapse progression-free survival (PR-PFS) and overall survival (PR-OS). In total, 109 patients were included in the study. Median DMFI was 25.3 (range: 3.4-188.2) months. Median PR-PFS in patients with DMFI of more than 24 months was 7.9 months [95% confidence interval (CI): 6.2-9.7] compared with 5.4 (95% CI: 4.2-6.7) months of those with shorter DMFI (P = 0.016). Median PR-OS was 15.6 months (95% CI: 13.6-17.6) in patients with DMFI of more than 24 months and 12.0 months (95% CI: 9.0-15.0) with DMFI of up to 24 months (P = 0.289). Multivariate Cox regression analysis showed that DMFI was independently and strongly associated with improved PR-PFS (adjusted hazard ratio = 3.21, 95% CI: 1.78-5.77, ≤ 24 vs. > 24 months) and longer PR-OS (adjusted hazard ratio: 2.09, 95% CI: 1.15-3.80, ≤ 24 vs. > 24 months). The present cohort study is one of the first to confirm the association of DMFI of more than 24 months with an indolent disease course, as shown by longer PR-PFS and PR-OS, in patients with relapsed stage IV melanoma treated by BRAF inhibitor/MEK inhibitor.
这项回顾性队列研究评估了在接受 BRAF 加或不加 MEK 抑制剂(BRAFi ± MEKi)治疗的复发性 BRAF 突变黑色素瘤患者中,无远处转移间隔(DMFI)的预后意义。将 DMFI 长达 24 个月的患者与 DMFI 超过 24 个月的患者进行比较,比较其复发后无进展生存期(PR-PFS)和总生存期(PR-OS)。该研究共纳入 109 例患者。DMFI 的中位数为 25.3(范围:3.4-188.2)个月。DMFI 超过 24 个月的患者 PR-PFS 的中位数为 7.9 个月(95%置信区间[CI]:6.2-9.7),而 DMFI 较短的患者为 5.4 个月(95%CI:4.2-6.7)(P = 0.016)。DMFI 超过 24 个月的患者 PR-OS 的中位数为 15.6 个月(95%CI:13.6-17.6),DMFI 达 24 个月的患者为 12.0 个月(95%CI:9.0-15.0)(P = 0.289)。多变量 Cox 回归分析显示,DMFI 与改善的 PR-PFS 独立且密切相关(调整后的危险比=3.21,95%CI:1.78-5.77,≤24 vs. >24 个月)和更长的 PR-OS(调整后的危险比:2.09,95%CI:1.15-3.80,≤24 vs. >24 个月)。本队列研究是第一个确认 DMFI 超过 24 个月与复发性 IV 期黑色素瘤患者疾病进程惰性相关的研究之一,这表现为 PR-PFS 和 PR-OS 更长,这些患者接受 BRAF 抑制剂/MEK 抑制剂治疗。