TY - JOUR
T1 - Early Detection of Acute and Early-Onset Cancer Therapy-Related Cardiac Dysfunction in Children With Cancer Using a Multiparametric Approach
T2 - Methodological Aspects of the EARLY Study
AU - Kouwenberg, Theodorus W.
AU - Grotenhuis, Heynric B.
AU - Kremer, Leontien C.M.
AU - de Baat, Esmée C.
AU - Beishuizen, Auke
AU - van Noesel, Max M.
AU - Kapusta, Livia
AU - Nievelstein, Rutger A.J.
AU - Velthuis, Birgitta K.
AU - Slieker, Martijn G.
AU - Leiner, Tim
AU - Hoeben, Bianca A.W.
AU - Mavinkurve-Groothuis, Annelies M.C.
AU - Feijen, Elizabeth A.M.
N1 - © 2026 The Author(s). Cancer Medicine published by John Wiley & Sons Ltd.
PY - 2026/5
Y1 - 2026/5
N2 - Background: Cancer therapy-related cardiac dysfunction (CTRCD) is among the most important adverse effects of treatment of childhood cancer. In the EARLY study (Early detection of acute and early-onset cARdiovascuLar toxicity in children with cancer using a multiparametric approach), cardiac function in children treated for cancer was monitored during and shortly after treatment, using advanced echocardiography, electrocardiography, and cardiac magnetic resonance (CMR) techniques. Methods: In this prospective pilot study, 100 children newly diagnosed with childhood cancer receiving anthracyclines as part of their cancer treatment were included. A subgroup of 30 children was included in the CMR sub-study. Echocardiography, electrocardiography, and CMR were performed before (T0), three and a half months after (T1), and one year after (T2) start of anthracycline treatment. In this article, we focus on the methodological aspects of the EARLY study, including patient enrollment and characteristics of the study cohort, as well as the feasibility of advanced echocardiography. Current Status: The last patient was included in August 2022. Follow-up for the last patient was finalized in August 2023. Follow-up was completed by 92% of the total study population and 97% of the CMR sub-study. Conclusions: Protocol adherence was high (92%–97%) and a full collection of data on each included individual was achieved. Advanced echocardiography, i.e., 4D ejection fraction and global longitudinal strain, was feasible in 76% and 69% of measurements, respectively. Cardiac outcomes during and shortly after treatment, as well as associations with known risk factors for CTRCD, such as anthracycline dose, dose of radiotherapy involving the heart, childhood cancer disease profile, age at diagnosis and sex will be reported in a future publication. The feasibility of the study allows for future insight into the correlation between early-onset CTRCD and heart failure during long-term follow-up of childhood cancer patients. Trial Registration: ClinicalTrials.gov identifier: NL-OMON22737.
AB - Background: Cancer therapy-related cardiac dysfunction (CTRCD) is among the most important adverse effects of treatment of childhood cancer. In the EARLY study (Early detection of acute and early-onset cARdiovascuLar toxicity in children with cancer using a multiparametric approach), cardiac function in children treated for cancer was monitored during and shortly after treatment, using advanced echocardiography, electrocardiography, and cardiac magnetic resonance (CMR) techniques. Methods: In this prospective pilot study, 100 children newly diagnosed with childhood cancer receiving anthracyclines as part of their cancer treatment were included. A subgroup of 30 children was included in the CMR sub-study. Echocardiography, electrocardiography, and CMR were performed before (T0), three and a half months after (T1), and one year after (T2) start of anthracycline treatment. In this article, we focus on the methodological aspects of the EARLY study, including patient enrollment and characteristics of the study cohort, as well as the feasibility of advanced echocardiography. Current Status: The last patient was included in August 2022. Follow-up for the last patient was finalized in August 2023. Follow-up was completed by 92% of the total study population and 97% of the CMR sub-study. Conclusions: Protocol adherence was high (92%–97%) and a full collection of data on each included individual was achieved. Advanced echocardiography, i.e., 4D ejection fraction and global longitudinal strain, was feasible in 76% and 69% of measurements, respectively. Cardiac outcomes during and shortly after treatment, as well as associations with known risk factors for CTRCD, such as anthracycline dose, dose of radiotherapy involving the heart, childhood cancer disease profile, age at diagnosis and sex will be reported in a future publication. The feasibility of the study allows for future insight into the correlation between early-onset CTRCD and heart failure during long-term follow-up of childhood cancer patients. Trial Registration: ClinicalTrials.gov identifier: NL-OMON22737.
KW - anthracyclines
KW - cardiac dysfunction
KW - cardiac magnetic resonance
KW - childhood cancer
KW - echocardiography
KW - Prospective Studies
KW - Humans
KW - Child, Preschool
KW - Neoplasms/drug therapy
KW - Infant
KW - Male
KW - Heart Diseases/diagnosis
KW - Cardiotoxicity/etiology
KW - Magnetic Resonance Imaging
KW - Pilot Projects
KW - Echocardiography/methods
KW - Adolescent
KW - Electrocardiography
KW - Antineoplastic Agents/adverse effects
KW - Female
KW - Child
KW - Early Diagnosis
KW - Anthracyclines/adverse effects
UR - https://www.scopus.com/pages/publications/105037767726
UR - https://www.mendeley.com/catalogue/917d2904-2bd9-31c4-adcc-17607c07e860/
U2 - 10.1002/cam4.71904
DO - 10.1002/cam4.71904
M3 - Article
C2 - 42070243
AN - SCOPUS:105037767726
SN - 2045-7634
VL - 15
JO - Cancer Medicine
JF - Cancer Medicine
IS - 5
M1 - e71904
ER -