Echocardiographic long-term follow-up of adult survivors of pediatric cancer treated with Dexrazoxane-Anthracyclines association.
Adult
Anthracyclines
/ administration & dosage
Antineoplastic Agents
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Cancer Survivors
Dexrazoxane
/ administration & dosage
Echocardiography
/ drug effects
Female
Follow-Up Studies
Humans
Male
Time Factors
Treatment Outcome
Young Adult
Anthracycline
Cardiotoxicity
Dexrazoxane
Strain echocardiography
Journal
International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291
Informations de publication
Date de publication:
15 01 2020
15 01 2020
Historique:
received:
10
04
2019
revised:
28
06
2019
accepted:
30
07
2019
pubmed:
20
8
2019
medline:
24
11
2020
entrez:
20
8
2019
Statut:
ppublish
Résumé
Cardiovascular disease is a well-recognized cause of increased late morbidity and mortality among survivors of childhood cancer treated with anthracyclines. Co-administration of Dexrazoxane has been shown to significantly reduce short-term and mid-term cardiotoxicity. Aim of this study was to assess cardiac function in long-term (>10 years) survivors of childhood tumors treated with dexrazoxane/anthracycline association. Twenty cancer survivors previously treated with co-administration of anthracyclines-dexrazoxane for childhood renal tumors or sarcoma and a control group of 20 healthy subjects were enrolled in the study. Echocardiographic measurements included 3D left ventricular (LV) ejection fraction (LVEF) and LV and right ventricular (RV) global longitudinal strain (GLS). Among cancer survivors group the median age at diagnosis was 5 years (1-17) and they were evaluated at median follow-up time of 21.5 years (10-26). No evidence of cardiac toxicity, as defined by current guidelines, was reported in all survivors. No significant differences in standard and deformation imaging parameters were observed between survivors and controls (3D LVEF 58 ± 3% vs 60 ± 5% p = NS; LV GLS -21 ± 1% vs -21 ± 2% p = NS; RV GLS -23 ± 2% vs -23 ± 5% p = NS). No second tumor was registered in dexrazoxane-treated survivors. Our findings may support the role of dexrazoxane as a useful strategy for cardio-protection in children undergoing anthracycline based treatment. However, large randomized trials are needed to confirm the cardio-protective role of dexrazoxane in pediatric setting at long-term follow-up.
Identifiants
pubmed: 31422879
pii: S0167-5273(19)31879-0
doi: 10.1016/j.ijcard.2019.07.096
pii:
doi:
Substances chimiques
Anthracyclines
0
Antineoplastic Agents
0
Dexrazoxane
048L81261F
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
271-275Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.