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.


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
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

595-603

Subventions

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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Auteurs

F Lynce (F)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.

A Barac (A)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.
MedStar Heart & Vascular Institute, Washington, DC, USA.

X Geng (X)

Department of Biostatistics, Bioinformatics & Biomathematics, Georgetown University Medical Center, Washington, DC, USA.

C Dang (C)

Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

A F Yu (AF)

Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

K L Smith (KL)

The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
The Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

C Gallagher (C)

Washington Cancer Institute, MedStar Washington Hospital Center, Washington, DC, USA.

P R Pohlmann (PR)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.

R Nunes (R)

The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
The Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

P Herbolsheimer (P)

AstraZeneca, Gaithersburg, MD, USA.

R Warren (R)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.

M B Srichai (MB)

MedStar Heart & Vascular Institute, Washington, DC, USA.
Department of Cardiology, MedStar Georgetown University Hospital, Washington, DC, USA.

M Hofmeyer (M)

MedStar Heart & Vascular Institute, Washington, DC, USA.

A Cunningham (A)

MedStar Health Research Institute, Hyattsville, MD, USA.

P Timothee (P)

MedStar Health Research Institute, Hyattsville, MD, USA.

F M Asch (FM)

MedStar Heart & Vascular Institute, Washington, DC, USA.
MedStar Health Research Institute, Hyattsville, MD, USA.

A Shajahan-Haq (A)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.

M T Tan (MT)

Department of Biostatistics, Bioinformatics & Biomathematics, Georgetown University Medical Center, Washington, DC, USA.

C Isaacs (C)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA.

S M Swain (SM)

Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 4000 Reservoir Road NW, 120 Building D, Washington, DC, 20057-1400, USA. sandra.swain@georgetown.edu.

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Classifications MeSH