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An evaluation of the safety of continuing trastuzumab despite overt left ventricular dysfunction.
Barron, C C; Alhussein, M M; Kaur, U; Cosman, T L; Tyagi, N K; Brown, M; Mukherjee, S D; Ellis, P M; Dhesy-Thind, S; Leong, D P.
Affiliation
  • Barron CC; Department of Medicine, McMaster University, Hamilton, ON.
  • Alhussein MM; Department of Medicine, McMaster University, Hamilton, ON.
  • Kaur U; Department of Medicine, University of Western Ontario, London, ON.
  • Cosman TL; Hamilton Health Sciences, Juravinski Hospital and Cancer Centre, Hamilton, ON.
  • Tyagi NK; School of Nursing, McMaster University, Hamilton, ON.
  • Brown M; Department of Oncology, McMaster University, Hamilton, ON.
  • Mukherjee SD; Hamilton Health Sciences, Juravinski Hospital and Cancer Centre, Hamilton, ON.
  • Ellis PM; Department of Oncology, McMaster University, Hamilton, ON.
  • Dhesy-Thind S; Department of Oncology, McMaster University, Hamilton, ON.
  • Leong DP; Department of Oncology, McMaster University, Hamilton, ON.
Curr Oncol ; 26(4): 240-246, 2019 08.
Article in En | MEDLINE | ID: mdl-31548803
ABSTRACT

Background:

The major limitation in the use of trastuzumab therapy is cardiotoxicity. We evaluated the safety of a strategy of continuing trastuzumab in patients with breast cancer despite mild, asymptomatic left ventricular impairment.

Methods:

Charts of consecutive patients referred to a cardio-oncology clinic from January 2015 to March 2017 for decline in left ventricular ejection fraction (lvef), defined as a fall of 10 percentage points or more, or a value of less than 50% during trastuzumab therapy, were reviewed. The primary outcome of interest was change in lvef, measured before and during trastuzumab exposure and up to 3 times after initiation of cardiac medications during a median of 9 months.

Results:

All 18 patients referred for decline in lvef chose to remain on trastuzumab and were included. All patients were treated with angiotensin converting-enzyme inhibitors or beta-blockers, or both. After initiation of cardiac medications, lvef increased over time by 4.6 percentage points (95% confidence interval 1.9 percentage points to 7.4 percentage points), approaching baseline values. Of the 18 patients, 17 (94%) were asymptomatic at all future visits. No deaths occurred in the group.

Conclusions:

Many patients with mildly reduced lvef and minimal heart failure symptoms might be able to continue trastuzumab without further decline in lvef, adverse cardiac events, or death when treated under the supervision of a cardiologist with close follow-up.
Subject(s)
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Full text: 1 Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / Ventricular Dysfunction, Left / Adrenergic beta-Antagonists / Trastuzumab Type of study: Observational_studies Limits: Aged / Female / Humans / Middle aged Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Angiotensin-Converting Enzyme Inhibitors / Ventricular Dysfunction, Left / Adrenergic beta-Antagonists / Trastuzumab Type of study: Observational_studies Limits: Aged / Female / Humans / Middle aged Language: En Year: 2019 Type: Article