2026
Long-term Subclinical Cardiotoxicity of Modern Cardiotoxic Treatment Protocols in Childhood Cancer Survivors Assessed by Cardiovascular Magnetic Resonance T1 Mapping and Circulatory Biomarkers
PANOVSKÝ, Roman; Marie TOMANDLOVÁ; Mary Luz MOJICA-PISCIOTTI; Tomáš KEPÁK; Jan MÁCHAL et al.Základní údaje
Originální název
Long-term Subclinical Cardiotoxicity of Modern Cardiotoxic Treatment Protocols in Childhood Cancer Survivors Assessed by Cardiovascular Magnetic Resonance T1 Mapping and Circulatory Biomarkers
Autoři
PANOVSKÝ, Roman; Marie TOMANDLOVÁ; Mary Luz MOJICA-PISCIOTTI; Tomáš KEPÁK; Jan MÁCHAL; Vera FEITOVA; Jan FRIČ; Marcela HORTOVÁ KOHOUTKOVÁ; Tomáš HOLEČEK; Josef TOMANDL ORCID; Lukáš OPATŘIL a Vladimír KINCL
Vydání
Cardiovascular Toxicology, Totowa, Humana Press, 2026, 1530-7905
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.700 v roce 2024
Označené pro přenos do RIV
Ne
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Cardiac magnetic resonance; Childhood cancer survivors; Anthracyclines; T1 mapping; Circulatory biomarkers
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 25. 2. 2026 09:47, Mgr. Tereza Miškechová
Anotace
V originále
Childhood cancer survivors (CCS) are at increased risk of developing heart disease due to the cardiotoxic effects of oncological treatment. This study aimed to investigate the long-term cardiotoxic effects of cancer therapy in CCS using a multimodal approach combining cardiac magnetic resonance (CMR) imaging and circulating blood biomarkers. A total of 117 CCS (mean age 24.7 +/- 5.2 years), at least five years post-treatment and in complete remission, were prospectively enrolled. All participants underwent CMR, including T1 mapping, and blood analysis for biomarkers of endothelial damage and oxidative stress. Parameters were compared with sex- and age-matched healthy control groups. Anthracycline treatment was administered in 82.9% of CCS (mean cumulative doxorubicin equivalent dose 231.7 +/- 92.0 mg/m(2)). Left ventricular ejection fraction and mitral annular plane systolic excursion were significantly reduced in CCS compared to controls (59.0 +/- 5.5% vs. 67.2 +/- 6.9%, p < 0.001; 12.5 +/- 1.7 mm vs. 13.9 +/- 2.2 mm, p = 0.001). Late gadolinium enhancement was detected in four CCS. No significant differences in global native T1 relaxation time or extracellular volume were observed. N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels remained within normal limits but correlated with native T1, ECV, and MAPSE. Levels of myeloperoxidase, big endothelin-1, and ischemia-modified albumin were significantly higher than in controls. Subclinical myocardial changes were detected in long-term CCS using CMR and circulating biomarkers. These findings support the utility of a multimodal approach for the early identification of individuals at increased cardiovascular risk after childhood cancer treatment.
Návaznosti
| LX22NPO5104, projekt VaV |
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