Department of Internal Medicine, UC Davis School of Medicine, Sacramento, CA.
Public Health Institute, Cancer Registry of Greater California, Sacramento, CA.
Clin Lung Cancer. 2019 Nov;20(6):477-483. doi: 10.1016/j.cllc.2019.06.005. Epub 2019 Jun 14.
Thymic malignancies are rare and there are limited contemporary population-based epidemiological studies for this uncommon cancer.
Adults aged 20 years and older diagnosed with thymic malignancies between 1988 and 2015 were identified from the California Cancer Registry (n = 1588). Trends in age-adjusted incidence rates were examined overall and according to race/ethnicity, and the proportion diagnosed according to stage was evaluated over time. Cox proportional hazards regression was used to estimate hazard ratios (HRs) for overall survival (OS), and Fine and Gray competing risks regression for cause-specific survival (CSS).
Age-adjusted incidence increased on average 2.08% per year over the study period (95% confidence interval [CI], 1.30%-2.86%; P < .0001), with an incidence of 0.277 cases per 100,000 in 2015. Incidence was highest among Asian/Pacific Islander and non-Hispanic black individuals. The proportion of unknown stage at diagnosis declined as localized diagnoses increased over time. Compared with patients with thymoma, those with thymic carcinoma had significantly worse OS (HR, 1.63; 95% CI, 1.33-2.01; P < .0001) and CSS (subdistribution HR, 2.99; 95% CI, 2.29-3.91; P < .0001). Advanced stage at diagnosis was also associated with worse survival. Surgical intervention was associated with better prognosis for patients with localized (HR, 0.08; 95% CI, 0.02-0.30; P = .0002) or regional disease (HR, 0.14; 95% CI, 0.06-0.34; P < .0001).
Thymic malignancy incidence is increasing in California. There was incidence variation across race/ethnicity, which warrants future study. These findings provide contemporary insight into the incidence and prognostic factors of thymic malignancies.
胸腺恶性肿瘤较为罕见,目前针对这种罕见癌症的当代人群流行病学研究有限。
从加利福尼亚癌症登记处(n=1588)中确定了 1988 年至 2015 年间诊断为胸腺恶性肿瘤的 20 岁及以上成年人。总体上以及根据种族/族裔检查了年龄调整发病率趋势,并随着时间的推移评估了按阶段诊断的比例。使用 Cox 比例风险回归估计总生存率(OS)的风险比(HR),并使用 Fine 和 Gray 竞争风险回归估计特定原因生存率(CSS)。
研究期间,年龄调整发病率平均每年增加 2.08%(95%置信区间[CI],1.30%-2.86%;P<0.0001),2015 年发病率为每 10 万人 0.277 例。发病率在亚洲/太平洋岛民和非西班牙裔黑人群体中最高。随着局部诊断的增加,诊断时未知阶段的比例下降。与胸腺瘤患者相比,胸腺癌患者的 OS(HR,1.63;95%CI,1.33-2.01;P<0.0001)和 CSS(亚分布 HR,2.99;95%CI,2.29-3.91;P<0.0001)明显更差。诊断时的晚期阶段也与生存不良相关。手术干预与局部(HR,0.08;95%CI,0.02-0.30;P=0.0002)或区域疾病(HR,0.14;95%CI,0.06-0.34;P<0.0001)患者的预后较好相关。
加利福尼亚州的胸腺恶性肿瘤发病率正在增加。种族/族裔之间存在发病率差异,这值得进一步研究。这些发现为胸腺恶性肿瘤的发病率和预后因素提供了当代的见解。