Meharry Medical College, Nashville, Tennessee.
Department of Pathology, Microbiology and Immunology, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee.
Cancer Epidemiol Biomarkers Prev. 2021 Jun;30(6):1149-1155. doi: 10.1158/1055-9965.EPI-20-1505. Epub 2021 Apr 1.
Appendiceal cancer incidence among individuals age < 50 years (early-onset appendiceal cancer) is rising with unknown etiologies. Distinct clinicopathologic/demographic features of early-onset appendiceal cancer remain unexplored. We compared patterns of appendiceal cancer among individuals by age of disease-onset.
Using the NIH/NCI's Surveillance, Epidemiology, and End Results program data, we identified individuals age 20+ years diagnosed with appendiceal cancer from 2007 to 2016. Cochran-Armitage trend tests and multinomial logistic regression models were used to examine age-related differences in clinicopathologic/demographic features of appendiceal cancer.
We identified 8,851 patients with appendiceal cancer during the 10-year study period. Histologic subtype, tumor grade, stage, sex and race/ethnicity all significantly differed by age of appendiceal cancer diagnosis. After adjustment for race/ethnicity, sex, stage, insurance status, and tumor grade, young patients were 82% more likely to be Hispanic [OR, 1.82; 95% confidence interval (CI), 1.48-2.25; < 0.001] and 4-fold more likely to be American Indian or Alaska Native (OR, 4.02; 95% CI, 1.77-9.16; = 0.0009) compared with late-onset cases. Patients with early-onset appendiceal cancer were also 2- to 3.5-fold more likely to be diagnosed with neuroendocrine tumors of the appendix (goblet cell carcinoid: OR, 1.96; 95% CI, 1.59-2.41; < 0.0001; carcinoid: OR, 3.52; 95% CI, 2.80-4.42; < 0.0001) compared with patients with late-onset appendiceal cancer. Among patients with neuroendocrine tumors, early-onset cases were also 45% to 61% less likely to present with high-grade (III-IV) tumors.
Approximately one in every three patients with appendiceal cancer is diagnosed before age 50 years in the United States. Appendiceal cancer in young patients is classified by distinct histologic and demographic features.
Early-onset appendiceal cancer determinants can inform discovery of risk factors and molecular biomarkers of appendiceal cancer in young patients, with implications for appendiceal cancer prevention, detection, and treatment.
50 岁以下人群(早发性阑尾癌)的阑尾癌发病率正在上升,但病因不明。早发性阑尾癌的独特临床病理/人口统计学特征仍未得到探索。我们比较了不同发病年龄人群的阑尾癌发病模式。
利用美国国立卫生研究院(NIH)/国家癌症研究所(NCI)的监测、流行病学和最终结果(SEER)计划数据,我们从 2007 年至 2016 年确定了 20 岁及以上诊断为阑尾癌的患者。采用 Cochran-Armitage 趋势检验和多项逻辑回归模型,研究阑尾癌的临床病理/人口统计学特征与年龄的关系。
在 10 年的研究期间,我们共发现 8851 例阑尾癌患者。组织学亚型、肿瘤分级、分期、性别和种族/民族均与阑尾癌诊断年龄显著相关。在调整种族/民族、性别、分期、保险状况和肿瘤分级后,年轻患者患阑尾癌的风险增加 82%,更有可能为西班牙裔[比值比(OR),1.82;95%置信区间(CI),1.48-2.25;<0.001],患阑尾癌的风险增加 4 倍,更有可能为美洲印第安人或阿拉斯加原住民(OR,4.02;95%CI,1.77-9.16;=0.0009)。与晚期发病病例相比,早发性阑尾癌患者更有可能被诊断为阑尾神经内分泌肿瘤[杯状细胞类癌(OR,1.96;95%CI,1.59-2.41;<0.0001);类癌(OR,3.52;95%CI,2.80-4.42;<0.0001)]。在神经内分泌肿瘤患者中,早发性阑尾癌患者的高级别(III-IV 级)肿瘤发病率也低 45%至 61%。
在美国,大约每 3 例阑尾癌患者中就有 1 例在 50 岁之前被诊断出。年轻患者的阑尾癌表现出独特的组织学和人口统计学特征。
早发性阑尾癌的决定因素可以为年轻患者的阑尾癌风险因素和分子生物标志物的发现提供信息,这对阑尾癌的预防、检测和治疗具有重要意义。