University of South Australia Allied Health and Human Performance, Adelaide, Australia; University of South Australia, Cancer Epidemiology and Population Health, Adelaide, Australia; Charles Perkins Centre, School of Medical Sciences, University of Sydney, Sydney, Australia.
University of South Australia Allied Health and Human Performance, Adelaide, Australia; University of South Australia, Cancer Epidemiology and Population Health, Adelaide, Australia; Flinders University, Health Data and Clinical Trials, Adelaide, Australia.
Cancer Epidemiol. 2022 Oct;80:102246. doi: 10.1016/j.canep.2022.102246. Epub 2022 Sep 5.
While age and stage at diagnosis are known to affect treatment choices and survival from colorectal cancer (CRC), few studies have investigated the extent to which these effects are influenced by comorbidity. In this study, we describe the occurrence of comorbidity in CRC cases in South Australia and associations of comorbidity with age, stage and the age-stage relationship. Furthermore, we report on the association of individual comorbidities with age and stage at diagnosis.
The South Australian Cancer Registry (SACR) provided CRC data (C18-C20, ICD-10) for 2004-2013 diagnoses. CRC data were linked with comorbidity data drawn from hospital records and health insurance claims. Logistic regression was used to model associations of comorbidity with age and stage.
For the 8462 CRC cases in this study, diabetes, peptic ulcer disease, and previous cancers were the most commonly recorded co-existing conditions. Most comorbidities were associated with older age, although some presented more frequently in younger people. Patients at both ends of the age spectrum (<50 and 80 + years) had an increased likelihood of CRC diagnosis at an advanced stage compared with other ages (50-79 years old). Adjusting for comorbidities moderated the association of older age with advanced stage. Conditions associated with advanced stage included dementia (OR = 1.25 (1.01-1.55)), severe liver disease (OR = 1.68 (1.04-2.70)), and a previous cancer (OR = 1.18 (1.08-1.28)).
Comorbidities are prevalent with CRC, especially in older people. These comorbidities differ in their associations with age at diagnosis and stage. Dementia and chronic heart failure were associated with older age whereas inflammatory bowel disease and alcohol access were associated with younger onset of the disease. Severe liver disease and dementia were associated with more advanced stage and rheumatic disease with less advanced stage. Comorbidities also interact with age at diagnosis and appear to vary the likelihood of advanced-stage disease. CRC patient have different association of age with stage depending on their comorbidity status.
虽然年龄和诊断时的分期已知会影响结直肠癌(CRC)的治疗选择和生存,但很少有研究调查这些影响在多大程度上受到合并症的影响。在这项研究中,我们描述了南澳大利亚 CRC 病例中的合并症发生情况,以及合并症与年龄、分期和年龄分期关系的关联。此外,我们还报告了个别合并症与诊断时年龄和分期的关联。
南澳大利亚癌症登记处(SACR)提供了 2004-2013 年诊断的 CRC 数据(C18-C20,ICD-10)。CRC 数据与从医院记录和健康保险索赔中提取的合并症数据进行了链接。使用逻辑回归模型来模拟合并症与年龄和分期的关联。
在本研究的 8462 例 CRC 病例中,糖尿病、消化性溃疡病和既往癌症是最常见的并存疾病。大多数合并症与年龄较大有关,尽管有些在年轻人中更为常见。与其他年龄组(50-79 岁)相比,年龄处于两端(<50 岁和 80 岁以上)的患者更有可能在晚期诊断出 CRC。调整合并症后,年龄较大与晚期分期的关联得到缓和。与晚期分期相关的疾病包括痴呆(OR=1.25(1.01-1.55))、严重肝脏疾病(OR=1.68(1.04-2.70))和既往癌症(OR=1.18(1.08-1.28))。
CRC 合并症很常见,尤其是在老年人中。这些合并症在与诊断时年龄和分期的关联上存在差异。痴呆和慢性心力衰竭与年龄较大有关,而炎症性肠病和酒精滥用与疾病发病年龄较小有关。严重肝脏疾病和痴呆与更晚期的疾病有关,而风湿性疾病与较晚期的疾病有关。合并症还与诊断时的年龄相互作用,似乎改变了晚期疾病的可能性。CRC 患者的年龄与分期的关联因合并症状态而异。