Morsani College of Medicine, University of Southern Florida, Tampa, FL, USA.
Discovery Research Group, College of Medicine and Health, University of Exeter, St Luke's Campus, Exeter, UK.
Fam Pract. 2021 Jul 28;38(4):425-431. doi: 10.1093/fampra/cmaa132.
Pre-existing conditions interfere with cancer diagnosis by offering diagnostic alternatives, competing for clinical attention or through patient surveillance.
To investigate associations between oesophagogastric cancer stage and pre-existing conditions.
Retrospective cohort study using Clinical Practice Research Datalink (CPRD) data, with English cancer registry linkage. Participants aged ≥40 years had consulted primary care in the year before their incident diagnosis of oesophagogastric cancer in 01/01/2010-31/12/2015. CPRD records pre-diagnosis were searched for codes denoting clinical features of oesophagogastric cancer and for pre-existing conditions, including those providing plausible diagnostic alternatives for those features. Logistic regression analysed associations between stage and multimorbidity (≥2 conditions; reference category: no multimorbidity) and having 'diagnostic alternative(s)', controlling for age, sex, deprivation and cancer site.
Of 2444 participants provided, 695 (28%) were excluded for missing stage, leaving 1749 for analysis (1265/1749, 72.3% had advanced-stage disease). Multimorbidity was associated with stage [odds ratio 0.63, 95% confidence interval (CI) 0.47-0.85, P = 0.002], with moderate evidence of an interaction term with sex (1.76, 1.08-2.86, P = 0.024). There was no association between alternative explanations and stage (odds ratio 1.18, 95% CI 0.87-1.60, P = 0.278).
In men, multimorbidity is associated with a reduced chance of advanced-stage oesophagogastric cancer, to levels seen collectively for women.
先前存在的疾病会通过提供诊断替代方案、争夺临床关注或通过患者监测来干扰癌症诊断。
研究食管癌和胃癌分期与先前存在的疾病之间的关系。
使用临床实践研究数据库(CPRD)数据进行回顾性队列研究,并与英国癌症登记处进行链接。参与者年龄≥40 岁,在 2010 年 1 月 1 日至 2015 年 12 月 31 日期间,在其确诊为食管癌和胃癌之前的一年中在初级保健机构就诊过。在 CPRD 记录中搜索表示食管癌和胃癌临床特征的代码,以及先前存在的疾病,包括那些为这些特征提供可能的诊断替代方案的疾病。使用逻辑回归分析分期与多种合并症(≥2 种疾病;参考类别:无多种合并症)和存在“诊断替代方案”之间的关联,并控制年龄、性别、贫困程度和癌症部位。
在所提供的 2444 名参与者中,有 695 名(28%)因分期缺失而被排除,剩余 1749 名用于分析(1265/1749,72.3%患有晚期疾病)。多种合并症与分期相关[比值比 0.63,95%置信区间(CI)0.47-0.85,P=0.002],且与性别存在中度交互作用(1.76,1.08-2.86,P=0.024)。替代解释与分期之间没有关联(比值比 1.18,95%CI 0.87-1.60,P=0.278)。
在男性中,多种合并症与晚期食管癌和胃癌的机会减少有关,与女性的总体水平相当。