Key result
Exposure to adjuvant fluoropyrimidine-based chemotherapy was associated with a significantly increased risk of cardiovascular disease (HR 2.11) among survivors of high-risk stage II-III colorectal cancer compared to noncancer controls.
Why the study?
With increasing survival of colorectal cancer, many long-term survivors are elderly with comorbidities, requiring assessment of long-term CVD incidence associated with adjuvant fluoropyrimidine-based chemotherapy.
Does adjuvant fluoropyrimidine-based chemotherapy increase the risk of incident cardiovascular disease in survivors of high-risk stage II-III colorectal cancer compared to noncancer controls?
Cohort (n=6,115)
Does adjuvant fluoropyrimidine-based chemotherapy increase the risk of incident cardiovascular disease in survivors of high-risk stage II-III colorectal cancer compared to noncancer controls?
Hazard Ratio: 2.11 (95% CI 1.39–3.2)
Absolute Event Rate: 5.4% vs 3.8%
p-value: p=<0.001
Exposure to adjuvant fluoropyrimidine-based chemotherapy is associated with a 2-fold increased risk of long-term cardiovascular disease among survivors of high-risk stage II-III colorectal cancer.
Supports vigilant CVD monitoring in CRC survivors on adjuvant chemotherapy; leaves open causality versus confounding.
BACKGROUND: The incidence and survival of colorectal cancer (CRC) are increasing. There is an increasing number of long-term survivors, many of whom are elderly and have comorbidities. We conducted a population-based study in Hong Kong to assess the long-term cardiovascular disease (CVD) incidence associated with adjuvant fluoropyrimidine-based chemotherapy among CRC survivors. PATIENTS AND METHODS: Using the population-based electronic medical database of Hong Kong, we identified adults who were diagnosed with high-risk stage II-III CRC and treated with radical surgery followed by adjuvant fluoropyrimidine-based chemotherapy between 2010 and 2019. We evaluated the cause-specific cumulative incidence of CVD (including ischemic heart disease, heart failure, cardiomyopathy, and stroke) using the flexible parametric competing risk modeling framework. The control group without a history of CVD was selected from among a noncancer random sample from primary care clinics in the same geographic area. RESULTS: We analyzed 1,037 treated patients with CRC and 5,078 noncancer controls. The adjusted cause-specific hazard ratio (HR) for CVD in the cancer cohort compared with the control group was 2.11 (95% CI, 1.39-3.20). The 1-, 5-, and 10-year cause-specific cumulative incidences were 2.0%, 4.5%, and 5.4% in the cancer cohort versus 1.2%, 3.0%, and 3.8% in the control group, respectively. Age at cancer diagnosis (HR per 5-year increase, 1.16; 95% CI, 1.08-1.24), male sex (HR, 1.40; 95% CI, 1.06-1.86), comorbidity (HR, 1.88; 95% CI, 1.36-2.61 for 1 comorbidity vs none, and HR, 6.61; 95% CI, 4.55-9.60 for ≥2 comorbidities vs none), diabetes (HR, 1.38; 95% CI, 1.04-1.84), hypertension (HR, 3.27; 95% CI, 2.39-4.50), and dyslipidemia/hyperlipidemia (HR, 2.53; 95% CI, 1.68-3.81) were associated with incident CVD. CONCLUSIONS: Exposure to adjuvant fluoropyrimidine-based chemotherapy was associated with an increased risk of CVD among survivors of high-risk stage II-III CRC. Cardiovascular risk monitoring of this group throughout cancer survivorship is advisable.
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Lee et al. (2022) conducted a cohort in High-risk stage II-III colorectal cancer (n=6,115). Adjuvant fluoropyrimidine-based chemotherapy vs. Noncancer controls without a history of CVD was evaluated on Incident cardiovascular disease (ischemic heart disease, heart failure, cardiomyopathy, and stroke) (HR 2.11, 95% CI 1.39-3.20, p=<0.001). Exposure to adjuvant fluoropyrimidine-based chemotherapy was associated with a significantly increased risk of cardiovascular disease (HR 2.11) among survivors of high-risk stage II-III colorectal cancer compared to noncancer controls.
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