Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
PLoS One. 2021 May 18;16(5):e0250939. doi: 10.1371/journal.pone.0250939. eCollection 2021.
The long-term survival of uveal melanoma patients in the US is not known. We compared long-term survival estimates using relative survival, excess absolute risk (EAR), Kaplan-Meier (KM), and competing risk analyses.
Population based cohort study.
Pooled databases from Surveillance, Epidemiology, and End Results data (SEER, SEER-9+SEER-13+SEER-18).
Overall Survival (OS), Metastasis Free Survival (MFS) and relative survival, computed directly or estimated via a model fitted to excess mortality.
There were 10678 cases of uveal melanoma spanning a period of 42 years (1975-2016). The median age at diagnosis was 63 years (range 3-99). Over half the patients were still alive at the end of 2016 (53%, 5625). The KM estimates of MFS were 0.729 (0.719, 0.74), 0.648 (0.633, 0.663), and 0.616 (0.596, 0.636) at 10, 20, and 30 years, respectively. The cumulative probabilities of melanoma metastatic death at 10, 20 and 30 years were 0.241 (0.236, 0.245), 0.289 (0.283, 0.294), and 0.301 (0.295, 0.307). In the first 5 years since diagnosis of uveal melanoma, the proportion of deaths attributable to uveal melanoma were 1.3 with rapid fall after 10 years. Death due to melanoma were rare beyond 20 years. Relative survival (RS) plateaued to ~60% across 20 to 30 years. EAR parametric modeling yielded a survival probability of 57%.
Relative survival methods can be used to estimate long term survival of uveal melanoma patients without knowing the exact cause of death. RS and EAR provide more realistic estimates as they compare the survival to that of a normal matched population. Death due to melanoma were rare beyond 20 years with normal life expectancy reached at 25 years after primary therapy.
目前尚不清楚美国葡萄膜黑色素瘤患者的长期生存情况。我们使用相对生存率、超额绝对风险(EAR)、Kaplan-Meier(KM)和竞争风险分析比较了长期生存估计。
基于人群的队列研究。
来自监测、流行病学和最终结果数据(SEER、SEER-9+SEER-13+SEER-18)的汇总数据库。
总生存(OS)、无转移生存(MFS)和相对生存率,直接计算或通过拟合超额死亡率的模型估计。
共有 10678 例葡萄膜黑色素瘤患者,随访时间为 42 年(1975-2016 年)。诊断时的中位年龄为 63 岁(范围 3-99 岁)。截至 2016 年底,仍有一半以上的患者存活(53%,5625 例)。KM 估计的 MFS 在 10、20 和 30 年时分别为 0.729(0.719,0.74)、0.648(0.633,0.663)和 0.616(0.596,0.636)。10、20 和 30 年时黑色素瘤转移死亡的累积概率分别为 0.241(0.236,0.245)、0.289(0.283,0.294)和 0.301(0.295,0.307)。在诊断后 5 年内,葡萄膜黑色素瘤导致的死亡比例为 1.3%,10 年后迅速下降。20 年以上黑色素瘤导致的死亡罕见。相对生存率(RS)在 20 至 30 年内稳定在 60%左右。EAR 参数模型得出的生存概率为 57%。
无需知道确切的死亡原因,相对生存率方法可用于估计葡萄膜黑色素瘤患者的长期生存情况。RS 和 EAR 提供了更现实的估计,因为它们将生存情况与正常匹配人群进行了比较。20 年以上黑色素瘤导致的死亡罕见,首次治疗后 25 年即可达到正常预期寿命。