Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston.
JAMA Oncol. 2017 Oct 1;3(10):1335-1342. doi: 10.1001/jamaoncol.2017.0589.
The incidence and prevalence of neuroendocrine tumors (NETs) are thought to be rising, but updated epidemiologic data are lacking.
To explore the evolving epidemiology and investigate the effect of therapeutic advances on survival of patients with NETs.
DESIGN, SETTING, AND PARTICIPANTS: A retrospective, population-based study using nationally representative data from the Surveillance, Epidemiology, and End Results (SEER) program was conducted to evaluate 64 971 patients with NETs from 1973 to 2012. Associated population data were used to determine annual age-adjusted incidence, limited-duration prevalence, and 5-year overall survival (OS) rates. Trends in survival from 2000 to 2012 were evaluated for the entire cohort as well as specific subgroups, including distant-stage gastrointestinal NETs and pancreatic NETs. Analyses were conducted between December 2015, and February 2017.
Neuroendocrine tumor incidence, prevalence, and OS rates.
Of the 64 971 cases of NETs, 34 233 (52.7%) were women. The age-adjusted incidence rate increased 6.4-fold from 1973 (1.09 per 100 000) to 2012 (6.98 per 100 000). This increase occurred across all sites, stages, and grades. In the SEER 18 registry grouping (2000-2012), the highest incidence rates were 1.49 per 100 000 in the lung, 3.56 per 100 000 in gastroenteropancreatic sites, and 0.84 per 100 000 in NETs with an unknown primary site. The estimated 20-year limited-duration prevalence of NETs in the United States on January 1, 2014, was 171 321. On multivariable analyses, the median 5-year OS rate varied significantly by stage, grade, age at diagnosis, primary site, and time period of diagnosis. The OS rate for all NETs improved from the 2000-2004 period to the 2009-2012 period (hazard ratio [HR], 0.79; 95% CI, 0.73-0.85). Even larger increases in OS between these periods were noted in distant-stage gastrointestinal NETs (HR, 0.71; 95% CI, 0.62-0.81) and distant-stage pancreatic NETs (HR, 0.56; 95% CI, 0.44-0.70).
The incidence and prevalence of NETs are steadily rising, possibly owing to detection of early-stage disease and stage migration. Survival for all NETs has improved over time, especially for distant-stage gastrointestinal NETs and pancreatic NETs in particular, reflecting improvement in therapies. These data will help to prioritize future research directions.
人们认为神经内分泌肿瘤(NET)的发病率和患病率正在上升,但缺乏最新的流行病学数据。
探讨不断变化的流行病学,并研究治疗进展对 NET 患者生存的影响。
设计、地点和参与者:使用全国代表性数据(SEER 计划)进行了一项回顾性、基于人群的研究,评估了 1973 年至 2012 年间的 64971 例 NET 患者。使用相关人群数据确定了每年年龄调整的发病率、有限持续时间的患病率和 5 年总生存率(OS)。评估了整个队列以及特定亚组(包括远处阶段胃肠 NET 和胰腺 NET)的 2000 年至 2012 年期间的生存趋势。分析于 2015 年 12 月至 2017 年 2 月进行。
神经内分泌肿瘤的发病率、患病率和 OS 率。
在 64971 例 NET 病例中,34233 例(52.7%)为女性。年龄调整后的发病率从 1973 年(1.09/100000)增加到 2012 年(6.98/100000),增加了 6.4 倍。这种增加发生在所有部位、阶段和等级。在 SEER18 登记组(2000-2012 年)中,发病率最高的是肺部的 1.49/100000,胃肠胰腺部位的 3.56/100000,以及未知原发部位的 NET 的 0.84/100000。2014 年 1 月 1 日,美国 NET 的估计 20 年有限持续时间患病率为 171321。在多变量分析中,中位 5 年 OS 率因阶段、分级、诊断时年龄、原发部位和诊断时间段而异。所有 NET 的 OS 率从 2000-2004 年期间到 2009-2012 年期间有所改善(风险比[HR],0.79;95%CI,0.73-0.85)。在这些时期之间,远处阶段胃肠 NET(HR,0.71;95%CI,0.62-0.81)和远处阶段胰腺 NET(HR,0.56;95%CI,0.44-0.70)的 OS 率有更大的提高。
NET 的发病率和患病率稳步上升,可能是由于早期疾病的检出和疾病阶段的迁移。随着时间的推移,所有 NET 的生存率都有所提高,特别是对于远处阶段的胃肠 NET 和胰腺 NET,这反映了治疗的改善。这些数据将有助于确定未来的研究方向。