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BRAF 抑制剂或联合 MEK 抑制剂治疗后复发黑色素瘤患者无远处转移间期的预后意义。

Prognostic significance of distant metastasis-free interval in patients with relapsed melanoma treated with BRAF with or without MEK inhibitors.

机构信息

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.

出版信息

Melanoma Res. 2019 Aug;29(4):428-434. doi: 10.1097/CMR.0000000000000562.

Abstract

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.

摘要

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。

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