Key result
Developing heart failure after chemotherapy for breast or haematologic cancer increased the risk of all-cause mortality by 67% compared to patients who did not develop heart failure (HR 1.67).
Why the study?
Does the development of heart failure following chemotherapy for breast or haematologic cancer increase mortality in cancer patients?
Cohort (n=15,987)
Does the development of heart failure following chemotherapy for breast or haematologic cancer increase mortality in cancer patients?
Effect estimate: HR 1.67 (95% CI 1.54-1.81)
p-value: p=<0.001
The development of heart failure following chemotherapy for breast or haematologic cancer occurs rapidly and significantly increases all-cause mortality, highlighting the critical need for cardiovascular monitoring in cancer survivors.
May warrant closer cardiac surveillance in chemotherapy recipients; leaves open whether HF prevention improves survival.
BACKGROUND: Cardiotoxicity resulting in heart failure is a devastating complication of cancer therapy. A patient may survive cancer only to develop heart failure (HF), which has a higher mortality rate than some cancers. AIM: This study aimed to describe the characteristics and outcomes of HF in patients with blood or breast cancer after chemotherapy treatment. METHODS: Queensland Cancer Registry, Death Registry and Hospital Administration records were linked (1996-2009). Patients were categorised as those with an index HF admission (that occurred after cancer diagnosis) and those without an index HF admission (non-HF). RESULTS: A total of 15 987 patients was included, and 1062 (6.6%) had an index HF admission. Median age of HF patients was 67 years (interquartile range 58-75) versus 54 years (interquartile range 44-64) for non-HF patients. More men than women developed HF (48.6% vs 29.5%), and a greater proportion in the HF group had haematological cancer (83.1%) compared with breast cancer (16.9%). After covariate adjustment, HF patients had increased mortality risk compared with non-HF patients (hazard ratios 1.67 (95% confidence interval, 1.54-1.81)), and 47% of the index HF admission occurred within 1 year from cancer diagnosis and 70% within 3 years. CONCLUSION: Cancer treatment may place patients at a greater risk of developing HF. The onset of HF occurred soon after chemotherapy, and those who developed HF had a greater mortality risk.
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Clark et al. (2016) conducted a cohort in Breast or haematologic cancer (n=15,987). Development of heart failure vs. No heart failure was evaluated on All-cause mortality (HR 1.67, 95% CI 1.54-1.81, p=<0.001). Developing heart failure after chemotherapy for breast or haematologic cancer increased the risk of all-cause mortality by 67% compared to patients who did not develop heart failure (HR 1.67).
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