Prediction of trastuzumab-induced cardiotoxicity in breast cancer patients receiving anthracycline-based chemotherapy.


Journal

Journal of echocardiography
ISSN: 1880-344X
Titre abrégé: J Echocardiogr
Pays: Japan
ID NLM: 101263153

Informations de publication

Date de publication:
06 2019
Historique:
received: 06 04 2018
accepted: 03 08 2018
revised: 01 08 2018
pubmed: 14 8 2018
medline: 19 6 2020
entrez: 13 8 2018
Statut: ppublish

Résumé

Adjuvant trastuzumab improved overall survival and reduced the risk for disease recurrence in women with breast cancers, because of its potential cardiotoxicity, careful monitoring of left ventricular (LV) function during treatment is required. This study investigates, whether myocardial strain imaging and level of N-terminal pro-brain natriuretic peptide (NT-pro BNP) could predict subsequent reduction in LVEF in breast cancer patients received adjuvant trastuzumab. 61 women with pathologically proven breast cancer HER-2 positive received AC (Doxorubicin-Cyclophosphamide) for 4 cycles, followed by paclitaxel with Trastuzumab were enrolled. Clinical, conventional echocardiographic parameters, myocardial strain imaging [global longitudinal peak systolic strain (GLS), radial and circumferential systolic strain] and level of NT pro-BNP were measured at baseline, after 3, 6, 9 and 12 months of trastuzumab therapy. Of 61 patients, 18 patients (29.5%) developed trastuzumab-induced cardiomyopathy (CM) at 6 and 9 months of therapy (LVEF declines ≥ 10%), GLS and radial strain significantly decreased in CM group at 3 months of trastuzumab treatment, the value of GLS at 3 months was the strongest predictors of cardiotoxicity its area under the curve (AUC 0.98) with an optimal cut-off for GLS (- 18%) having 92.5% sensitivity and 83% specificity. NT-pro BNP levels were not predictive of later trastuzumab-induced cardiac dysfunction. Myocardial strain imaging has been able to predict pre-clinical changes in LV systolic function and GLS is an independent early predictor of subsequent reduction in EF in breast cancer patients treated with trastuzumab.

Sections du résumé

BACKGROUND
Adjuvant trastuzumab improved overall survival and reduced the risk for disease recurrence in women with breast cancers, because of its potential cardiotoxicity, careful monitoring of left ventricular (LV) function during treatment is required.
METHODS
This study investigates, whether myocardial strain imaging and level of N-terminal pro-brain natriuretic peptide (NT-pro BNP) could predict subsequent reduction in LVEF in breast cancer patients received adjuvant trastuzumab. 61 women with pathologically proven breast cancer HER-2 positive received AC (Doxorubicin-Cyclophosphamide) for 4 cycles, followed by paclitaxel with Trastuzumab were enrolled. Clinical, conventional echocardiographic parameters, myocardial strain imaging [global longitudinal peak systolic strain (GLS), radial and circumferential systolic strain] and level of NT pro-BNP were measured at baseline, after 3, 6, 9 and 12 months of trastuzumab therapy.
RESULTS
Of 61 patients, 18 patients (29.5%) developed trastuzumab-induced cardiomyopathy (CM) at 6 and 9 months of therapy (LVEF declines ≥ 10%), GLS and radial strain significantly decreased in CM group at 3 months of trastuzumab treatment, the value of GLS at 3 months was the strongest predictors of cardiotoxicity its area under the curve (AUC 0.98) with an optimal cut-off for GLS (- 18%) having 92.5% sensitivity and 83% specificity. NT-pro BNP levels were not predictive of later trastuzumab-induced cardiac dysfunction.
CONCLUSION
Myocardial strain imaging has been able to predict pre-clinical changes in LV systolic function and GLS is an independent early predictor of subsequent reduction in EF in breast cancer patients treated with trastuzumab.

Identifiants

pubmed: 30099714
doi: 10.1007/s12574-018-0394-4
pii: 10.1007/s12574-018-0394-4
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Trastuzumab P188ANX8CK

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

76-83

Commentaires et corrections

Type : CommentIn

Références

J Am Coll Cardiol. 2014 Mar 4;63(8):809-16
pubmed: 24291281
Int J Cardiol. 2013 Oct 15;168(6):5465-7
pubmed: 24090744
J Clin Oncol. 2008 Mar 10;26(8):1201-3
pubmed: 18227525
J Am Soc Echocardiogr. 2008 Dec;21(12):1290-2
pubmed: 19041570
Am J Cardiol. 2011 May 1;107(9):1375-80
pubmed: 21371685
Circ Res. 2011 Mar 4;108(5):619-28
pubmed: 21372293
Curr Oncol. 2008 Jan;15(1):24-35
pubmed: 18317582
Circ Cardiovasc Imaging. 2012 Sep 1;5(5):596-603
pubmed: 22744937
J Clin Oncol. 2008 Mar 10;26(8):1231-8
pubmed: 18250349
Heart. 2010 May;96(9):701-7
pubmed: 20424152
Ann Oncol. 2012 Apr;23(4):897-902
pubmed: 21828361
J Clin Oncol. 2005 Nov 1;23(31):7811-9
pubmed: 16258083
J Am Coll Cardiol. 2011 May 31;57(22):2263-70
pubmed: 21616287
Eur Heart J. 1997 Mar;18(3):507-13
pubmed: 9076390
CA Cancer J Clin. 2011 Mar-Apr;61(2):69-90
pubmed: 21296855
Cardiovasc Ultrasound. 2007 Aug 30;5:27
pubmed: 17760964
Asia Pac J Clin Oncol. 2011 Sep;7(3):276-80
pubmed: 21884439
J Clin Oncol. 2012 Nov 1;30(31):3792-9
pubmed: 22987084
J Clin Oncol. 2010 Jul 20;28(21):3422-8
pubmed: 20530280
Anticancer Res. 2013 Apr;33(4):1717-20
pubmed: 23564821
Am Heart J. 2009 Aug;158(2):294-301
pubmed: 19619708
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300
pubmed: 20610543
J Clin Oncol. 2002 Mar 1;20(5):1215-21
pubmed: 11870163
J Ultrasound Med. 2011 Jan;30(1):71-83
pubmed: 21193707
N Engl J Med. 2005 Oct 20;353(16):1659-72
pubmed: 16236737
N Engl J Med. 2001 Mar 15;344(11):783-92
pubmed: 11248153
N Engl J Med. 2005 Oct 20;353(16):1673-84
pubmed: 16236738
J Breast Cancer. 2014 Dec;17(4):363-9
pubmed: 25548585
N Engl J Med. 2000 Apr 13;342(15):1077-84
pubmed: 10760308
Pharmacol Res. 2013 Dec;78:41-8
pubmed: 24171840
J Am Soc Echocardiogr. 2013 May;26(5):493-8
pubmed: 23562088

Auteurs

Wafaa S El-Sherbeny (WS)

Cardiovascular Medicine Department, Faculty of Medicine, Tanta University, Tanta, Egypt. Wfelsherbeny@gmail.com.

Nesreen M Sabry (NM)

Clinical Oncology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

Radwa M Sharbay (RM)

Clinical Pathology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.

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