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@ARTICLE{Anker:304276,
author = {M. S. Anker and A. A. Mahabadi and M. Totzeck and M. Tewes
and M. Shahzeb Khan and R. I. Mincu and U. B. Hendgen-Cotta
and L. Michel and B. Mathew and O. Drescher and M. Schuler
and U. Keller$^*$ and K. Rieger and J. Ahn and L.
Bullinger$^*$ and D. P. Modest$^*$ and C. Denecke and L.
Kretzler and L. V. Ramer and D. Krug and U. Landmesser and
L. Lehmann and N. Frey and S. Bercker and U. Laufs and M.
Böhm and F. Mahfoud and B. Merkely and M. Diek and J.
Butler and A. Veiser and T. Heise and M. Hellmich and M.
Placzek and T. Friede and S. D. Anker and T. Rassaf},
title = {{H}eart {F}ailure {T}herapy in {P}atients with {A}dvanced
{C}ancer {R}eceiving {S}pecialized {P}alliative {C}are
({EMPATICC} trial).},
journal = {European heart journal},
volume = {nn},
issn = {0195-668X},
address = {Oxford},
publisher = {Oxford University Press},
reportid = {DKFZ-2025-01817},
pages = {nn},
year = {2025},
note = {epub},
abstract = {Advanced cancer may resemble a heart failure (HF)-like
phenotype marked by cardiac wasting, dyspnoea, congestion,
and/or physical dysfunction. The trial evaluated safety and
efficacy of HF therapy among patients with advanced cancer
receiving specialized palliative care to improve patients'
self-care ability.Patients with stage 4 solid tumours with a
life expectancy of 1-6 months receiving specialized
palliative care were enrolled. Patients were required to
meet at least two cardiovascular risk criteria and at least
one criterion for functional limitation. Participants were
randomized 1:1 to receive optimised HF therapy (up to 4
drugs: sacubitril/valsartan, empagliflozin, ivabradine,
ferric carboxymaltose) or placebo in a double-blind setting.
The primary hierarchical endpoint included: (1) days alive
and able to wash oneself, (2) ability to walk 4 m, (3)
self-reported patient global assessment (PGA) of subjective
well-being, during the 30-day placebo-controlled phase.In 5
centers, 93 patients were randomized. The primary endpoint
did not differ between groups (win ratio 0.95, $95\%$
confidence interval [CI] 0.57-1.58; P=0.83). Overall,
mortality was $32\%$ at 30 days (not different between
groups). In patients alive at 30 days, HF therapy reduced
N-terminal pro-B-type natriuretic peptide levels by $41\%$
(P=0.040), increased left ventricular ejection fraction by
$2.9\%$ (P=0.036), and improved PGA scores (odds ratio 0.22,
$95\%$ CI 0.06-0.75; P=0.016).In a population with advanced
cancer receiving specialized palliative care and high early
mortality, optimised HF therapy did not improve patients'
self-care ability. Among survivors at 30 days, improvements
in quality of life measures and cardiac biomarkers suggest
potential benefit of individualized HF therapy, which is
hypothesis generating and needs validation.},
keywords = {Heart failure therapy (Other) / cardiac wasting (Other) /
clinical trial (Other) / end-stage cancer (Other) /
palliative care (Other)},
cin = {BE01},
ddc = {610},
cid = {I:(DE-He78)BE01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40884070},
doi = {10.1093/eurheartj/ehaf705},
url = {https://inrepo02.dkfz.de/record/304276},
}