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Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood

INTRODUCTION: Late cardiotoxicity is a known complication of anthracycline therapy but the long-term effects of low cumulative doses are not well documented. We studied late cardiotoxicity in survivors of childhood acute lymphoblastic leukemia (ALL) treated with low anthracycline doses 10 to 20 year...

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Autores principales: Vandecruys, Els, Mondelaers, Veerle, De Wolf, Daniel, Benoit, Yves, Suys, Bert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279635/
https://www.ncbi.nlm.nih.gov/pubmed/21630046
http://dx.doi.org/10.1007/s11764-011-0186-6
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author Vandecruys, Els
Mondelaers, Veerle
De Wolf, Daniel
Benoit, Yves
Suys, Bert
author_facet Vandecruys, Els
Mondelaers, Veerle
De Wolf, Daniel
Benoit, Yves
Suys, Bert
author_sort Vandecruys, Els
collection PubMed
description INTRODUCTION: Late cardiotoxicity is a known complication of anthracycline therapy but the long-term effects of low cumulative doses are not well documented. We studied late cardiotoxicity in survivors of childhood acute lymphoblastic leukemia (ALL) treated with low anthracycline doses 10 to 20 years earlier. METHODS: Seventy-seven ALL survivors who received a cumulative anthracycline dose <250 mg/m² and were at least 10 years after treatment were evaluated for signs of clinical heart failure. Cardiac function was assessed by echocardiography including tissue Doppler measurements of the septal mitral annulus in 37 ALL survivors 10.6–18.3 years (median 13.3 years) after anthracycline treatment with cumulative doses of 180 (n = 19) or 240 mg/m² (n = 18). The control group consisted of 30 healthy volunteers matched for age, sex, BSA, and BMI. RESULTS: No clinical relevant cardiotoxicity was found. Left ventricular shortening fraction (SF) was significantly reduced in male ALL survivors. Three of the 19 male ALL survivors had an SF below 30%. Male ALL survivors showed a significantly lower early filling velocity to atrial contraction velocity ratio but myocardial velocity during early filling was comparable between patients and controls. ALL survivors had a significantly longer isovolumetric relaxation time (IVRT). Thirty percent of the ALL survivors have an abnormal IVRT compared to the normal range of the controls. CONCLUSION AND IMPLICATIONS FOR CANCER SURVIVORS: At a median of 13.3 years after exposure to cumulative doses of anthracyclines of 180 or 240 mg/m², no clinical relevant cardiotoxicity was found but subclinical cardiac abnormalities were present in 30% of the patients.
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spelling pubmed-32796352012-03-01 Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood Vandecruys, Els Mondelaers, Veerle De Wolf, Daniel Benoit, Yves Suys, Bert J Cancer Surviv Article INTRODUCTION: Late cardiotoxicity is a known complication of anthracycline therapy but the long-term effects of low cumulative doses are not well documented. We studied late cardiotoxicity in survivors of childhood acute lymphoblastic leukemia (ALL) treated with low anthracycline doses 10 to 20 years earlier. METHODS: Seventy-seven ALL survivors who received a cumulative anthracycline dose <250 mg/m² and were at least 10 years after treatment were evaluated for signs of clinical heart failure. Cardiac function was assessed by echocardiography including tissue Doppler measurements of the septal mitral annulus in 37 ALL survivors 10.6–18.3 years (median 13.3 years) after anthracycline treatment with cumulative doses of 180 (n = 19) or 240 mg/m² (n = 18). The control group consisted of 30 healthy volunteers matched for age, sex, BSA, and BMI. RESULTS: No clinical relevant cardiotoxicity was found. Left ventricular shortening fraction (SF) was significantly reduced in male ALL survivors. Three of the 19 male ALL survivors had an SF below 30%. Male ALL survivors showed a significantly lower early filling velocity to atrial contraction velocity ratio but myocardial velocity during early filling was comparable between patients and controls. ALL survivors had a significantly longer isovolumetric relaxation time (IVRT). Thirty percent of the ALL survivors have an abnormal IVRT compared to the normal range of the controls. CONCLUSION AND IMPLICATIONS FOR CANCER SURVIVORS: At a median of 13.3 years after exposure to cumulative doses of anthracyclines of 180 or 240 mg/m², no clinical relevant cardiotoxicity was found but subclinical cardiac abnormalities were present in 30% of the patients. Springer US 2011-06-01 2012 /pmc/articles/PMC3279635/ /pubmed/21630046 http://dx.doi.org/10.1007/s11764-011-0186-6 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Vandecruys, Els
Mondelaers, Veerle
De Wolf, Daniel
Benoit, Yves
Suys, Bert
Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title_full Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title_fullStr Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title_full_unstemmed Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title_short Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
title_sort late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279635/
https://www.ncbi.nlm.nih.gov/pubmed/21630046
http://dx.doi.org/10.1007/s11764-011-0186-6
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