Abstract
Background
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.
Methods
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.
Results
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)).
Conclusion
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.
Highlights
- • Most comorbidities are more likely to be present in older CRC cases.
- • Cases at both ends of the age spectrum tend to have more advanced stages.
- • Comorbidities weaken the association of older age with advanced stage of CRC.
- • Dementia, liver disease and previous cancer are associated with advanced stage CRC.
1Background
CRC is more common among older people and, with an ageing world population, increases in the prevalence of CRC and other co-existing chronic conditions are expected . Comorbidities are more prevalent in older cases and can significantly impact the course of CRC by reducing resilience, and affecting treatment choices and outcomes . Additionally, several studies have highlighted an increasing proportion of people younger than 50 years with CRC . Some comorbidities such as Inflammatory bowel disease (IBD) can be risk factors for CRC. Diagnosis of CRC in this population can be delayed where other diagnoses are considered earlier . It’s well-established that comorbidities are more common among CRC cases of more advanced age, but the association of individual comorbidities with age has not been thoroughly investigated.
Population-based bowel screening has been implemented in Australia and many other countries to detect CRC at an earlier stage and improve survival . Still, almost half of CRCs are diagnosed at advanced stages . Few studies have investigated the impact of age and comorbidity on CRC stage, but available data indicate that both young and old ages (younger than 50 and older than 60 years) increase the likelihood of diagnosis at an advanced stage . Comorbidities can also impact on the cancer diagnostic process and stage through a number of mechanisms . Results of different studies on associations of comorbidities with CRC advanced stage have been inconsistent .
The purpose of this study is: to describe the occurrence of common comorbidities within CRC in South Australia; and to use population-based data to investigate how age at diagnosis varies with presence of comorbidities. Subsequently, we explore the presence, if any, of interactions between age and comorbidity, with advanced stage CRC.
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