2D-echocardiography vs cardiac MRI strain: a prospective cohort study in patients with HER2-positive breast cancer undergoing trastuzumab.


Journal

Cardiovascular ultrasound
ISSN: 1476-7120
Titre abrégé: Cardiovasc Ultrasound
Pays: England
ID NLM: 101159952

Informations de publication

Date de publication:
09 Nov 2021
Historique:
received: 10 04 2021
accepted: 18 10 2021
entrez: 10 11 2021
pubmed: 11 11 2021
medline: 12 11 2021
Statut: epublish

Résumé

We aimed to study the predictive value of early two-dimensional echocardiography (2DE) speckle tracking (ST) for left ventricular ejection fraction (LVEF) changes during trastuzumab treatment for HER2-positive breast cancer. HER2-positive breast cancer patients receiving trastuzumab, with or without anthracycline, underwent 2DE-ST at baseline and after 3 and 6 months (m) trastuzumab. Cardiac magnetic resonance (CMR) imaging (with ST) was performed at baseline and 6 m. We studied the correlation between 2DE-ST- and CMR-derived global longitudinal strain (GLS) and global radial strain (GRS) measured at the same time. Additionally, we associated baseline and 3 m 2DE-ST measurements with later CMR-LVEF, and with cardiotoxicity, defined as CMR-LVEF < 45% and/or absolute decline > 10% during trastuzumab. Forty-seven patients were included. Median baseline LVEF was 60.4%. GLS measurements based on 2DE-ST and CMR showed weak correlation (Pearson's r = 0.33; p = 0.041); GRS measurements were uncorrelated (r = 0.09; p = 0.979). 2DE-LVEF at baseline and 3 m, and 2DE-ST-GLS at 3 m were predictive of CMR-LVEF at 6 m. In contrast, the change in 2DE-ST-GLS at 3 m was predictive of the change in CMR-LVEF at 6 m, whereas the change in 2DE-LVEF was not. Importantly, the 11 patients who developed cardiotoxicity (28%) had larger 2DE-ST-GLS change at 3 m than those who did not (median 5.2%-points versus 1.7%-points; odds ratio for 1% difference change 1.81, 95% confidence interval 1.11-2.93; p = 0.016; explained variance 0.34). Correlations between 2DE-ST and CMR-derived measurements are weak. Nevertheless, ST-measurements appeared useful to improve the performance of 2DE in predicting LVEF changes after 6 m of trastuzumab treatment.

Sections du résumé

BACKGROUND BACKGROUND
We aimed to study the predictive value of early two-dimensional echocardiography (2DE) speckle tracking (ST) for left ventricular ejection fraction (LVEF) changes during trastuzumab treatment for HER2-positive breast cancer.
METHODS METHODS
HER2-positive breast cancer patients receiving trastuzumab, with or without anthracycline, underwent 2DE-ST at baseline and after 3 and 6 months (m) trastuzumab. Cardiac magnetic resonance (CMR) imaging (with ST) was performed at baseline and 6 m. We studied the correlation between 2DE-ST- and CMR-derived global longitudinal strain (GLS) and global radial strain (GRS) measured at the same time. Additionally, we associated baseline and 3 m 2DE-ST measurements with later CMR-LVEF, and with cardiotoxicity, defined as CMR-LVEF < 45% and/or absolute decline > 10% during trastuzumab.
RESULTS RESULTS
Forty-seven patients were included. Median baseline LVEF was 60.4%. GLS measurements based on 2DE-ST and CMR showed weak correlation (Pearson's r = 0.33; p = 0.041); GRS measurements were uncorrelated (r = 0.09; p = 0.979). 2DE-LVEF at baseline and 3 m, and 2DE-ST-GLS at 3 m were predictive of CMR-LVEF at 6 m. In contrast, the change in 2DE-ST-GLS at 3 m was predictive of the change in CMR-LVEF at 6 m, whereas the change in 2DE-LVEF was not. Importantly, the 11 patients who developed cardiotoxicity (28%) had larger 2DE-ST-GLS change at 3 m than those who did not (median 5.2%-points versus 1.7%-points; odds ratio for 1% difference change 1.81, 95% confidence interval 1.11-2.93; p = 0.016; explained variance 0.34).
CONCLUSIONS CONCLUSIONS
Correlations between 2DE-ST and CMR-derived measurements are weak. Nevertheless, ST-measurements appeared useful to improve the performance of 2DE in predicting LVEF changes after 6 m of trastuzumab treatment.

Identifiants

pubmed: 34753503
doi: 10.1186/s12947-021-00266-x
pii: 10.1186/s12947-021-00266-x
pmc: PMC8576921
doi:

Substances chimiques

Trastuzumab P188ANX8CK

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

35

Informations de copyright

© 2021. The Author(s).

Références

JAMA Netw Open. 2018 Aug 3;1(4):e181456
pubmed: 30646130
Circ Cardiovasc Imaging. 2017 Nov;10(11):
pubmed: 29138230
Breast Cancer Res Treat. 2021 Apr;186(3):851-862
pubmed: 33394273
J Cardiovasc Magn Reson. 2019 Aug 8;21(1):46
pubmed: 31391036
J Clin Oncol. 2012 Aug 10;30(23):2876-84
pubmed: 22802310
Sci Rep. 2019 Aug 5;9(1):11296
pubmed: 31383914
J Am Soc Echocardiogr. 2018 Sep;31(9):1021-1033.e1
pubmed: 29936007
J Am Coll Cardiol. 2021 Feb 2;77(4):392-401
pubmed: 33220426
Elife. 2019 Oct 09;8:
pubmed: 31596231
Circ Cardiovasc Imaging. 2012 Sep 1;5(5):596-603
pubmed: 22744937
Eur Heart J. 2000 Aug;21(16):1387-96
pubmed: 10952828
J Am Soc Echocardiogr. 2013 May;26(5):493-8
pubmed: 23562088
J Am Coll Cardiol. 2013 Jan 8;61(1):77-84
pubmed: 23199515
JAMA Cardiol. 2019 Oct 1;4(10):1007-1018
pubmed: 31433450
J Am Coll Cardiol. 2010 Jan 19;55(3):213-20
pubmed: 20117401
J Cardiovasc Magn Reson. 2016 Aug 26;18(1):51
pubmed: 27561421
J Am Soc Echocardiogr. 2011 Mar;24(3):277-313
pubmed: 21338865
J Clin Oncol. 2014 Jul 1;32(19):2078-99
pubmed: 24799465
Medicine (Baltimore). 2016 Nov;95(44):e5195
pubmed: 27858859
Br J Cancer. 2009 Mar 10;100(5):684-92
pubmed: 19259090
Am J Cardiol. 2011 May 1;107(9):1375-80
pubmed: 21371685
Ann Oncol. 2020 Feb;31(2):171-190
pubmed: 31959335
Breast. 2020 Aug;52:33-44
pubmed: 32361151
J Am Soc Echocardiogr. 2015 May;28(5):587-96
pubmed: 25577185
Am J Cardiol. 2006 Jun 1;97(11):1661-6
pubmed: 16728234
Rev Port Cardiol. 2017 Jan;36(1):9-15
pubmed: 27955938
J Cardiovasc Magn Reson. 2017 Sep 1;19(1):66
pubmed: 28863780
Eur Heart J Cardiovasc Imaging. 2014 Oct;15(10):1063-93
pubmed: 25239940
Eur J Echocardiogr. 2009 Jan;10(1):82-8
pubmed: 18490270
J Am Soc Echocardiogr. 2015 Oct;28(10):1171-1181, e2
pubmed: 26209911
J Am Coll Cardiol. 2019 Jun 11;73(22):2859-2868
pubmed: 31171092
Acta Cardiol Sin. 2016 Sep;32(5):560-564
pubmed: 27713604
J Am Soc Echocardiogr. 2008 Dec;21(12):1318-25
pubmed: 19041575
Eur Heart J Cardiovasc Imaging. 2016 May;17(5):525-32
pubmed: 26377901
J Am Soc Echocardiogr. 2014 Mar;27(3):292-301
pubmed: 24440110
Breast Cancer Res Treat. 2019 Jun;175(3):595-603
pubmed: 30852761

Auteurs

Nathalie I Bouwer (NI)

Department of Internal Medicine , Albert Schweitzer Hospital, 3300 AK, Dordrecht, The Netherlands. n.i.bouwer@asz.nl.
Department of Cardiology, Albert Schweitzer Hospital, Dordrecht, The Netherlands. n.i.bouwer@asz.nl.

Crista Liesting (C)

Department of Cardiology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

Marcel J M Kofflard (MJM)

Department of Cardiology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

Jasper J Brugts (JJ)

Department of Cardiology, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Marc C J Kock (MCJ)

Department of Radiology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

Jos J E M Kitzen (JJEM)

Department of Internal Medicine , Albert Schweitzer Hospital, 3300 AK, Dordrecht, The Netherlands.

Mark-David Levin (MD)

Department of Internal Medicine , Albert Schweitzer Hospital, 3300 AK, Dordrecht, The Netherlands.

Eric Boersma (E)

Department of Cardiology, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH