Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.
Clin Epidemiol. 2012;4 Suppl 2(Suppl 2):39-44. doi: 10.2147/CLEP.S33315. Epub 2012 Aug 17.
We examined the completeness of TNM staging of small-cell (SCLC) and nonsmall- cell (NSCLC) lung cancer in the national Danish Cancer Registry (DCR) and whether staging varied by year of diagnosis, gender, age, degree of comorbidity, or presence of histopathological diagnosis.
We identified all patients with SCLCs and NSCLCs registered in the DCR during 2004-2009 and examined the completeness of their TNM registrations. Completeness was defined as the number of recorded individuals with TNM divided by the total number of patients. Completeness was calculated for TNM, T, N, and M individually, overall, and by year of diagnosis, gender, age at diagnosis, and comorbidity. Data regarding comorbidity was obtained from the Danish National Patient Register (DNPR). We performed separate analyses for patients with a histopathologically verified diagnosis of NSCLC. Finally, we designed an algorithm to categorize tumors with missing TNM components as limited, extensive, or distant disease.
Overall TNM staging completeness was 77.5% (95% confidence interval (CI): 76.1%-78.8%) for SCLC and 77.9% (95% CI: 77.3%-78.4%) for NSCLC. Completeness did not vary by gender and increased during the study period. The proportion of staged patients was lower among patients above 80 years of age or with medium to high levels of comorbidity.
Overall TNM completeness for SCLC and NSCLC in the Danish Cancer Registry is high, but decreases with increasing levels of comorbidity and at ages greater than 80 years. Researchers should be aware of these potential sources of bias.
我们检查了丹麦癌症登记处(DCR)中小细胞肺癌(SCLC)和非小细胞肺癌(NSCLC)的 TNM 分期的完整性,以及分期是否因诊断年份、性别、年龄、合并症严重程度或组织病理学诊断的存在而有所不同。
我们确定了 2004-2009 年期间在 DCR 中登记的所有 SCLC 和 NSCLC 患者,并检查了他们的 TNM 登记的完整性。完整性定义为记录的具有 TNM 的个体数量与患者总数的比值。分别计算了 TNM、T、N 和 M 的完整性,以及整体完整性,以及按诊断年份、性别、诊断时的年龄和合并症严重程度计算的完整性。关于合并症的数据来自丹麦国家患者登记处(DNPR)。我们对具有组织病理学证实的 NSCLC 诊断的患者进行了单独的分析。最后,我们设计了一种算法,将缺失 TNM 成分的肿瘤归类为局限性、广泛性或远处疾病。
SCLC 的总体 TNM 分期完整性为 77.5%(95%置信区间(CI):76.1%-78.8%),NSCLC 为 77.9%(95% CI:77.3%-78.4%)。完整性不受性别影响,并在研究期间增加。在 80 岁以上或合并症程度中到高度的患者中,分期患者的比例较低。
丹麦癌症登记处的 SCLC 和 NSCLC 的总体 TNM 完整性较高,但随着合并症严重程度的增加和年龄超过 80 岁而降低。研究人员应该意识到这些潜在的偏倚来源。