Yu Jun, Blackford Amanda L, Dal Molin Marco, Wolfgang Christopher L, Goggins Michael
Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Department of Oncology, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Gut. 2015 Nov;64(11):1783-9. doi: 10.1136/gutjnl-2014-308653. Epub 2015 Jan 30.
Although pancreatic ductal adenocarcinoma is considered a rapidly progressive disease, mathematical models estimate that it takes many years for an initiating pancreatic cancer cell to grow into an advanced stage cancer. In order to estimate the time it takes for a pancreatic cancer to progress through different tumor, node, metastasis (TNM) stages, we compared the mean age of patients with pancreatic cancers of different sizes and stages.
Patient age, tumour size, stage and demographic information were analysed for 13,131 patients with pancreatic ductal adenocarcinoma entered into the National Cancer Institute's Surveillance, Epidemiology and End Results (SEER) database. Multiple linear regression models for age were generated, adjusting for patient ethnicity, gender, tumour location and neoplastic grades.
African-American ethnicity and male gender were associated with an earlier age at diagnosis. Patients with stage I cancers (mean age 64.8 years) were on average 1.3 adjusted years younger at diagnosis than those with stage IV cancers (p=0.001). Among patients without distant metastases, those with T1 stage cancers were on average 1.06 and 1.19 adjusted years younger, respectively, than patients with T3 or T4 cancers (p=0.03 for both). Among patients with stage IIB cancers, those with T1/T2 cancers were 0.79 adjusted years younger than those with T3 cancers (p=0.06). There was no significant difference in the mean adjusted age of patients with stage IA versus stage IB cancers.
These results are consistent with the hypothesis that once pancreatic ductal adenocarcinomas become detectable clinically progression from low-stage to advanced-stage disease is rapid.
尽管胰腺导管腺癌被认为是一种进展迅速的疾病,但数学模型估计,一个起始的胰腺癌细胞发展为晚期癌症需要数年时间。为了估计胰腺癌进展至不同肿瘤、淋巴结、转移(TNM)分期所需的时间,我们比较了不同大小和分期的胰腺癌患者的平均年龄。
对录入美国国立癌症研究所监测、流行病学和最终结果(SEER)数据库的13131例胰腺导管腺癌患者的年龄、肿瘤大小、分期和人口统计学信息进行分析。生成了年龄的多元线性回归模型,并对患者种族、性别、肿瘤位置和肿瘤分级进行了校正。
非裔美国人种族和男性与诊断时年龄较早相关。I期癌症患者(平均年龄64.8岁)诊断时的校正年龄比IV期癌症患者平均小1.3岁(p = 0.001)。在无远处转移的患者中,T1期癌症患者的校正年龄分别比T3或T4期癌症患者平均小1.06岁和1.19岁(两者p均= 0.03)。在IIB期癌症患者中,T1/T2期癌症患者的校正年龄比T3期癌症患者小0.79岁(p = 0.06)。IA期与IB期癌症患者的平均校正年龄无显著差异。
这些结果与以下假设一致,即一旦胰腺导管腺癌在临床上可被检测到,从低分期到高分期疾病的进展迅速。