Morehouse School of Medicine, Atlanta, Georgia, USA.
Cancer. 2013 Jul 15;119(14):2602-10. doi: 10.1002/cncr.28108. Epub 2013 May 14.
Paranasal sinus squamous cell carcinomas (PNSSCC) account for 3% of all head and neck malignancies. There has been little information on the trends in incidence and survival, and no randomized trials have been conducted to guide therapy.
Patients with PNSSCC reported to the Surveillance, Epidemiology, and End Results (SEER) Program from 1973 through 2009 were categorized by sex, age, year of diagnosis, primary site, stage, and treatment. The incidence and survival were then compared across different demographic and disease-related categories by calculating rate ratios (RRs) and mortality hazard ratios along with the corresponding 95% confidence intervals (CIs).
In total, 2553 patients with PNSSCC were identified. While incidence of PNSSCC showed a gradual decline, survival remained largely unchanged. The proportion of patients with advanced disease decreased from 14.7% during the period from 1983 to 1992 to 12.4% during 1993-2002 and to 9.5% during 2003-2009. Compared with whites, incidence was higher among African Americans (RR 1.63; 95% CI, 1.39, 1.90) and among all other racial groups (RR, 1.78; 95% CI: 1.53-2.07). After adjusting for age, sex, disease stage, tumor site, and treatment, mortality among African American patients also was increased (hazard ratio, 1.22; 95% CI, 1.04-1.43). Among patients with localized disease, the relation between race and mortality was no longer evident once the results were controlled for tumor classification.
The current findings point to racial disparities in the incidence of PNSSCC and, to a lesser extent, in the outcome of patients with PNSSCC. Although there has been a decline in the proportion of patients presenting with advanced PNSSCC, the overall survival remained stable over time.
鼻窦鳞状细胞癌(PNSSCC)占所有头颈部恶性肿瘤的 3%。关于发病率和生存率的趋势,信息很少,也没有进行过随机试验来指导治疗。
1973 年至 2009 年,向监测、流行病学和最终结果(SEER)计划报告的 PNSSCC 患者按性别、年龄、诊断年份、原发部位、分期和治疗进行分类。然后通过计算率比(RR)和死亡率风险比以及相应的 95%置信区间(CI),比较不同人口统计学和疾病相关类别之间的发病率和生存率。
共确定了 2553 例 PNSSCC 患者。尽管 PNSSCC 的发病率呈逐渐下降趋势,但生存率基本保持不变。晚期疾病患者的比例从 1983 年至 1992 年的 14.7%下降到 1993 年至 2002 年的 12.4%,再到 2003 年至 2009 年的 9.5%。与白人相比,非裔美国人的发病率更高(RR1.63;95%CI,1.39,1.90),所有其他种族群体的发病率也更高(RR1.78;95%CI:1.53-2.07)。调整年龄、性别、疾病分期、肿瘤部位和治疗后,非裔美国患者的死亡率也有所增加(风险比,1.22;95%CI,1.04-1.43)。在局部疾病患者中,一旦控制肿瘤分类,种族与死亡率之间的关系就不再明显。
目前的研究结果表明,PNSSCC 的发病率存在种族差异,在一定程度上也存在 PNSSCC 患者预后的种族差异。尽管晚期 PNSSCC 患者的比例有所下降,但总体生存率随时间保持稳定。