Key result
EMPATICC trial tests optimized heart failure therapy to improve function and well-being in advanced cancer.
Why the study?
Does optimized HF therapy improve functional ability and well-being in patients with advanced cancer at risk of cardiac wasting?
RCT (n=93)
Double-blind
1:1
Yes
Does optimized HF therapy improve functional ability and well-being in patients with advanced cancer at risk of cardiac wasting?
The EMPATICC trial is a proof-of-concept study evaluating whether optimized heart failure therapy can improve functional capacity and well-being in patients with end-stage cancer and cardiac wasting.
Aims End‐stage cancer may resemble a heart failure (HF)‐like phenotype marked by cardiac wasting, dysfunction, and symptoms such as dyspnoea, congestion, and impaired physical function. The EMPATICC (EMPower the heArt of patients with TermInal Cancer using Cardiac medicines) trial evaluates the safety and efficacy of optimized HF therapy in patients with advanced cancer to improve self‐care ability. Methods EMPATICC is a multicentre, investigator‐initiated, randomized, double‐blind, controlled, proof‐of‐concept trial employing a joint cardio‐oncology care approach. Patients were randomized 1:1 to optimized HF therapy (sacubitril/valsartan, empagliflozin, ivabradine, ferric carboxymaltose) plus usual care, or usual care alone, for 30 days, followed by a 30‐day open‐label extension. Eligible patients had stage IV solid tumours (per Union for International Cancer Control), were receiving palliative care, had a 1–6 month life expectancy, and were on optimized analgesia. At baseline, first patients had to meet ≥2 criteria of the following indicating cardiovascular risk: heart rate ≥70 bpm, N‐terminal pro‐B‐type natriuretic peptide ≥600 pg/ml, elevated high‐sensitivity troponin, left ventricular ejection fraction <55%, left ventricular mass loss >15%, transferrin saturation <20%, or moderate/high likelihood of HF with preserved ejection fraction (based on the HFA‐PEFF score); and they had to meet at least one criterion of the following indicating functional limitation: ≥6 s to walk 4 m, inability to wash ≥3 days of the last 7 days, or symptoms of dyspnoea at rest. Enrolment ended 30 January 2025; 93 patients completed randomization. The primary endpoint is a hierarchical composite (analysed by win ratio): (1) days alive and able to wash, (2) 4 m walking ability, and (3) patient global assessment of well‐being. Conclusions EMPATICC evaluates whether HF therapy can improve function and well‐being in advanced cancer, potentially reshaping care in this population.
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Anker et al. (2025) conducted an RCT in Advanced cancer (n=93). Optimized HF therapy (sacubitril/valsartan, empagliflozin, ivabradine, ferric carboxymaltose) vs. Usual care alone was evaluated on Hierarchical composite of days alive and able to wash, 4 m walking ability, and patient global assessment of well-being. The EMPATICC trial is designed to evaluate whether optimized heart failure therapy improves function and well-being in 93 patients with advanced cancer, with results pending.
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