Dutch Institute for Clinical Auditing.
Department of Medical Oncology, Amsterdam UMC, VU University Medical Center, Cancer Center Amsterdam.
Am J Clin Oncol. 2021 Feb 1;44(2):82-89. doi: 10.1097/COC.0000000000000786.
The aim of this study was to evaluate treatment patterns and overall survival (OS) of patients with BRAFV600 wild-type and BRAFV600-mutant advanced melanoma in the Netherlands.
We selected patients of 18 years and over, diagnosed between 2016 and 2017 with unresectable stage IIIC or IV melanoma, registered in the Dutch Melanoma Treatment Registry. To assess the association of BRAFV600-mutation status with OS we used the Cox proportional-hazards model.
A total of 642 BRAFV600 wild-type and 853 mutant patients were included in the analysis. Median OS did not differ significantly between both groups, 15.2 months (95% confidence interval [CI]: 13.2-19.2) versus 20.6 months (95% CI: 18.3-25.0). Survival rates at 6 and 12 months were significantly lower for BRAFV600 wild-type patients compared with BRAFV600-mutant patients, 72.0% (95% CI: 68.6-75.6) and 56.0% (95% CI: 52.2-60.0) versus 83.4% (95% CI: 80.9-85.9) and 65.7% (95% CI: 62.6-69.0). Two-year survival was not significantly different between both groups, 41.1% (95% CI: 37.2-45.3) versus 47.0% (95% CI: 43.6-60.6). Between 0 and 10 months, BRAFV600 wild-type patients had a decreased survival with a hazard ratio for OS of 2.00 (95% CI: 1.62-2.46) but this effect disappeared after 10 months. At 12 months, BRAFV600-mutant patients had started with second-line systemic treatment more often compared with BRAFV600 wild-type patients (50% vs. 19%).
These results suggest that advanced BRAFV600 wild-type melanoma patients have worse survival than BRAFV600-mutated patients during the first 10 months after diagnosis because of less available treatment options.
本研究旨在评估荷兰 BRAFV600 野生型和 BRAFV600 突变型晚期黑色素瘤患者的治疗模式和总生存期(OS)。
我们选择了 2016 年至 2017 年间诊断为不可切除 III C 期或 IV 期黑色素瘤、年龄在 18 岁及以上的患者,并在荷兰黑色素瘤治疗登记处进行了登记。为了评估 BRAFV600 突变状态与 OS 的关联,我们使用了 Cox 比例风险模型。
共纳入 642 例 BRAFV600 野生型和 853 例突变型患者进行分析。两组患者的中位 OS 无显著差异,分别为 15.2 个月(95%CI:13.2-19.2)和 20.6 个月(95%CI:18.3-25.0)。BRAFV600 野生型患者的 6 个月和 12 个月生存率明显低于 BRAFV600 突变型患者,分别为 72.0%(95%CI:68.6-75.6)和 56.0%(95%CI:52.2-60.0),而 83.4%(95%CI:80.9-85.9)和 65.7%(95%CI:62.6-69.0)。两组患者的 2 年生存率无显著差异,分别为 41.1%(95%CI:37.2-45.3)和 47.0%(95%CI:43.6-60.6)。在 0 至 10 个月期间,BRAFV600 野生型患者的生存率下降,OS 的风险比为 2.00(95%CI:1.62-2.46),但在 10 个月后这种效应消失。在 12 个月时,BRAFV600 突变型患者开始接受二线系统治疗的比例明显高于 BRAFV600 野生型患者(50%比 19%)。
这些结果表明,在诊断后的前 10 个月,晚期 BRAFV600 野生型黑色素瘤患者的生存状况比 BRAFV600 突变型患者差,这是由于治疗选择较少。