Prospective evaluation of the cardiac safety of HER2-targeted therapies in patients with HER2-positive breast cancer and compromised heart function: the SAFE-HEaRt study.
Ado-Trastuzumab Emtansine
Adrenergic beta-Antagonists
/ therapeutic use
Adult
Aged
Angiotensin-Converting Enzyme Inhibitors
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ administration & dosage
Breast Neoplasms
/ drug therapy
Female
Humans
Maytansine
/ administration & dosage
Middle Aged
Molecular Targeted Therapy
/ adverse effects
Neoplasm Staging
Pilot Projects
Prospective Studies
Receptor, ErbB-2
/ metabolism
Trastuzumab
/ administration & dosage
Treatment Outcome
Ventricular Dysfunction, Left
/ chemically induced
Breast cancer
Cardiac dysfunction
Cardiac safety
Carvedilol
HER2-targeted therapy
Journal
Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
received:
25
02
2019
accepted:
01
03
2019
pubmed:
11
3
2019
medline:
15
11
2019
entrez:
11
3
2019
Statut:
ppublish
Résumé
HER2-targeted therapies have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectively tests whether these therapies can be safely administered without interruptions in patients with cardiac dysfunction. Patients with stage I-IV HER2-positive breast cancer candidates for trastuzumab, pertuzumab or ado-trastuzumab emtansine (TDM-1), with left ventricular ejection fraction (LVEF) 40-49% and no symptoms of heart failure (HF) were enrolled. All patients underwent cardiology visits, serial echocardiograms and received beta blockers and ACE inhibitors unless contraindicated. The primary endpoint was completion of the planned HER2-targeted therapies without developing either a cardiac event (CE) defined as HF, myocardial infarction, arrhythmia or cardiac death or significant asymptomatic worsening of LVEF. The study was considered successful if planned oncology therapy completion rate was at least 30%. Of 31 enrolled patients, 30 were evaluable. Fifteen patients were treated with trastuzumab, 14 with trastuzumab and pertuzumab, and 2 with TDM-1. Mean LVEF was 45% at baseline and 46% at the end of treatment. Twenty-seven patients (90%) completed the planned HER2-targeted therapies. Two patients experienced a CE and 1 had an asymptomatic worsening of LVEF to ≤ 35%. This study provides safety data of HER2-targeted therapies in patients with breast cancer and reduced LVEF while receiving cardioprotective medications and close cardiac monitoring. Our results demonstrate the importance of collaboration between cardiology and oncology providers to allow for delivery of optimal oncologic care to this unique population.
Identifiants
pubmed: 30852761
doi: 10.1007/s10549-019-05191-2
pii: 10.1007/s10549-019-05191-2
pmc: PMC6534513
doi:
Substances chimiques
Adrenergic beta-Antagonists
0
Angiotensin-Converting Enzyme Inhibitors
0
Antibodies, Monoclonal, Humanized
0
Maytansine
14083FR882
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
pertuzumab
K16AIQ8CTM
Trastuzumab
P188ANX8CK
Ado-Trastuzumab Emtansine
SE2KH7T06F
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
595-603Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA051008
Pays : United States
Organisme : Genentech
ID : ML28685
Organisme : NCI NIH HHS
ID : P30CA051008 [PI: LM Weiner]
Pays : United States
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