Dutch Institute for Clinical Auditing, Rijnsburgerweg 10, Leiden, 2333AA, the Netherlands; Department of Medical Oncology, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333ZA, the Netherlands.
Department of Biomedical Data Sciences, Leiden University Medical Center, Einthovenweg 20, Leiden, 2333ZC, the Netherlands.
Eur J Cancer. 2021 Feb;144:242-251. doi: 10.1016/j.ejca.2020.11.028. Epub 2020 Dec 26.
The treatment landscape has completely changed for advanced melanoma. We report survival outcomes and the differential impact of prognostic factors over time in daily clinical practice.
From a Dutch nationwide population-based registry, patients with advanced melanoma diagnosed from 2013 to 2017 were analysed (n = 3616). Because the proportional hazards assumption was violated, a multivariable Cox model restricted to the first 6 months and a multivariable landmark Cox model from 6 to 48 months were used to assess overall survival (OS) of cases without missing values. The 2017 cohort was excluded from this analysis because of the short follow-up time.
Median OS of the 2013 and 2016 cohort was 11.7 months (95% confidence interval [CI]: 10.4-13.5) and 17.7 months (95% CI: 14.9-19.8), respectively. Compared with the 2013 cohort, the 2016 cohort had superior survival in the Cox model from 0 to 6 months (hazard ratio [HR] = 0.55 [95% CI: 0.43-0.72]) and in the Cox model from 6 to 48 months (HR = 0.68 [95% CI: 0.57-0.83]). Elevated lactate dehydrogenase levels, distant metastases in ≥3 organ sites, brain and liver metastasis and Eastern Cooperative Oncology Group performance score of ≥1 had stronger association with inferior survival from 0 to 6 months than from 6 to 48 months. BRAF-mutated melanoma had superior survival in the first 6 months (HR = 0.50 [95% CI: 0.42-0.59]).
CONCLUSION(S): Prognosis for advanced melanoma in the Netherlands has improved from 2013 to 2016. Prognostic importance of most evaluated factors was higher in the first 6 months after diagnosis. BRAF-mutated melanoma was only associated with superior survival in the first 6 months.
晚期黑色素瘤的治疗格局已完全改变。我们报告了在日常临床实践中生存结果和随时间推移的预后因素的差异影响。
从荷兰全国基于人群的登记处,分析了 2013 年至 2017 年诊断为晚期黑色素瘤的患者(n=3616)。由于违反了比例风险假设,因此使用多变量 Cox 模型限制在前 6 个月和多变量地标 Cox 模型从 6 至 48 个月来评估无缺失值病例的总生存(OS)。由于随访时间短,2017 队列未纳入该分析。
2013 年和 2016 年队列的中位 OS 分别为 11.7 个月(95%置信区间[CI]:10.4-13.5)和 17.7 个月(95%CI:14.9-19.8)。与 2013 年队列相比,2016 年队列在 Cox 模型中 0 至 6 个月时的生存优势(风险比[HR]为 0.55 [95%CI:0.43-0.72])和 Cox 模型中 6 至 48 个月时的生存优势(HR 为 0.68 [95%CI:0.57-0.83])更高。乳酸脱氢酶水平升高、≥3 个器官部位的远处转移、脑和肝转移以及东部合作肿瘤组表现评分≥1 与 0 至 6 个月时的生存预后比 6 至 48 个月时的生存预后更差的关联更强。BRAF 突变型黑色素瘤在前 6 个月的生存优势更高(HR=0.50 [95%CI:0.42-0.59])。
荷兰晚期黑色素瘤的预后自 2013 年至 2016 年有所改善。大多数评估因素的预后重要性在诊断后 6 个月内更高。BRAF 突变型黑色素瘤仅与前 6 个月的生存优势相关。