Summary
September 2006, Vol. 5, No. 5, Pages 619-629 , DOI 10.1517/14740338.5.5.619

Cardiac dysfunction associated with trastuzumab

Karen Lisa Smith1, Chau Dang2 & Andrew D Seidman2
1Fellow in Medical Oncology/Hematology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA
2Memorial Sloan-Kettering Cancer Center, Department of Medicine, Breast Cancer Medicine Service, 1275 York Avenue, New York, NY 10021, USA.
Author for correspondence



The HER2/neu gene is amplified in 25% of breast cancers, leading to HER2 protein overexpression and shortened overall survival and time to relapse. Trastuzumab is a humanised, monoclonal antibody against HER2, which improves survival for women with metastatic HER2-overexpressing breast cancer and reduces the risk of recurrence in women with early stage HER2-overexpressing breast cancer. Cardiac toxicity was an unexpected finding in the pivotal Phase III trial leading to the approval of trastuzumab, and prospective cardiac monitoring has, therefore, been incorporated into more recent clinical trials of trastuzumab. This article reviews the cardiac toxicity findings in key trastuzumab clinical trials and clinical characteristics of trastuzumab-associated cardiac toxicity.

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Forward Links to Citing Articles

Michael J Baumann, Beda M Stadler, Monique Vogel. (2007) Potential applications of designed ankyrin repeat proteins in diagnostics and therapeutics. Expert Opinion on Medical Diagnostics 1:3, 409-421
Online publication date: 1-Nov-2007.
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Authors:
Karen Lisa Smith
Chau Dang
Andrew D Seidman
Keywords:
breast cancer
cardiac toxicity
trastuzumab