Key result
Modified HFA-ICOS tool predicts cardiovascular complications in cancer patients with a ~0.70 C-statistic.
Why the study?
The Heart Failure Association and International Cardio-Oncology Society risk tool was developed from expert consensus, leaving its quantitative prognostic value uncertain in unselected cancer populations.
Does a modified HFA-ICOS tool predict cardiovascular complications in cancer patients?
Cohort (n=2,290)
No
Does a modified HFA-ICOS tool predict cardiovascular complications in cancer patients?
A modified HFA-ICOS risk tool effectively stratifies cardiovascular risk in cancer patients, providing quantitative validation for the expert consensus-based method.
May support CV risk stratification in cancer patients; extends expert consensus but remains hypothesis-generating pending prospective validation.
BACKGROUND: The 2022 European Society of Cardiology Cardio-oncology Guidelines recommend the Heart Failure Association and International Cardio-Oncology Society risk stratification tool to predict cardiovascular disease (CVD) risk in cancer patients. Developed from expert consensus rather than mathematical derivation, its quantitative prognostic value in unselected cancer populations remains uncertain. OBJECTIVES: The objective of the study was to assess the prognostic utility of a modified Heart Failure Association and International Cardio-Oncology Society tool, excluding biomarkers and imaging, in predicting CVD complications in cancer patients, thereby providing a quantitative correlate to an expert consensus-based method. METHODS: We included 2,290 cancer patients from the third follow-up of the Trøndelag Health study, diagnosed within 4 years of participation, and followed through 2023. Cancer therapy details were obtained from the Norwegian Cancer Registry. The primary outcome was a composite of myocardial infarction, heart failure hospitalization, stroke, or CVD mortality, identified via national registries. RESULTS: The mean age was 65.8 years; 48% were female. The most common cancers were gastrointestinal (23%), prostate (19%), and breast (12%). The median follow-up was 6.9 years. The modified tool classified 28% as low-, 35% moderate-, 34% high-, and 3% very high-risk. CVD incidence rose across categories: 7%, 21%, 29%, and 37% (P < 0.001). The C-statistic was 0.696 (95% CI: 0.674-0.718), and 0.746 (95% CI: 0.676-0.812) among anthracycline-treated patients. Within the low-to-moderate group, event rates ranged from 6% to 8% (0-1 points) to 24% to 27% (3-4 points). CONCLUSIONS: The tool stratifies CVD risk in cancer patients and may guide tailored follow-up and cardioprotection. Heterogeneity within moderate-risk patients highlights the need for refinement to improve individualized assessment.
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Gynnild et al. (2025) conducted a cohort in Cancer (n=2,290). Modified HFA-ICOS risk stratification tool was evaluated on Composite of myocardial infarction, heart failure hospitalization, stroke, or CVD mortality (C-statistic 0.696, 95% CI 0.674-0.718, p=<0.001). A modified HFA-ICOS risk stratification tool predicted cardiovascular complications in cancer patients with a C-statistic of 0.696, showing progressively higher event rates across risk categories.
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