Key result
Risk prediction models incorporating age, sex, smoking, radiotherapy, and anthracycline treatment predicted coronary heart disease and heart failure in Hodgkin lymphoma survivors with moderate discrimination (AUC 0.68-0.74).
Why the study?
Previous efforts to predict treatment-related cardiovascular disease risk mostly focused on childhood cancer survivors, leaving risk prediction models for adolescent and adult Hodgkin lymphoma survivors needed.
Can a risk prediction model accurately estimate the 20- and 30-year risk of coronary heart disease and heart failure in survivors of adolescent/adult Hodgkin lymphoma?
Cohort (n=2,141)
Yes
Can a risk prediction model accurately estimate the 20- and 30-year risk of coronary heart disease and heart failure in survivors of adolescent/adult Hodgkin lymphoma?
Effect estimate: AUC 0.74 (95% CI 0.70 to 0.77)
A newly developed and validated risk prediction model can identify Hodgkin lymphoma survivors at high risk for coronary heart disease and heart failure up to 30 years post-treatment, facilitating targeted screening.
May inform targeted CVD screening in Hodgkin lymphoma survivors; leaves open prospective validation before changing practice.
PURPOSE: Previous efforts to predict absolute risk of treatment-related cardiovascular diseases (CVDs) have mostly focused on childhood cancer survivors. We aimed to develop prediction models for risk of coronary heart disease (CHD) and heart failure (HF) for survivors of adolescent/adult Hodgkin lymphoma (HL). METHODS: For model development, we used a multicenter cohort including 1,433 5-year HL survivors treated between 1965 and 2000 and age 18-50 years at HL diagnosis, with complete data on administered chemotherapy regimens, radiotherapy volumes and doses, and cardiovascular follow-up. Using cause-specific hazard models, covariate-adjusted cumulative incidences for CHD and HF were estimated in the presence of competing risks of death because of other causes than CHD and HF. Age at HL diagnosis, sex, smoking status, radiotherapy, and anthracycline treatment were included as predictors. External validation for the CHD model was performed using a Canadian cohort of 708 HL survivors treated between 1988 and 2004 and age 18-50 years at HL diagnosis. RESULTS: After a median follow-up of 24 years, 341 survivors had developed CHD and 102 had HF. We were able to predict CHD and HF risk at 20 and 30 years after treatment with moderate to good overall calibration and moderate discrimination (areas under the curve: 0.68-0.74), which was confirmed by external validation for the CHD model (areas under the curve: 0.73-0.74). On the basis of our model including prescribed mediastinal radiation dose, 30-year risks ranged from 4% to 78% for CHD and 3% to 46% for HF, depending on risk factors. CONCLUSION: We developed and validated prediction models for CHD and HF with good overall calibration and moderate discrimination. These models can be used to identify HL survivors who might benefit from targeted screening for CVD and early treatment for CVD risk factors.
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Vries et al. (2022) conducted a cohort in Hodgkin lymphoma (5-year survivors) (n=2,141). Hodgkin lymphoma treatment (mediastinal radiotherapy and anthracyclines) and clinical risk factors vs. Lower or no exposure to cardiotoxic treatments and risk factors was evaluated on Discrimination (AUC) of the coronary heart disease dose prediction model at 20 years (AUC 0.74, 95% CI 0.70 to 0.77). Risk prediction models incorporating age, sex, smoking, radiotherapy, and anthracycline treatment predicted coronary heart disease and heart failure in Hodgkin lymphoma survivors with moderate discrimination (AUC 0.68-0.74).
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