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January 13, 2004Journal of Clinical Oncology283 citations

Clinical Cardiac Tolerability of Trastuzumab

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EPEdith A. PerezRRRichard J. Rodeheffer

Key Points

  • To provide an updated assessment of the incidence, clinical course, mechanisms, and management of trastuzumab-induced cardiac dysfunction in HER2-positive breast cancer.
  • Synthesized data from pivotal trials and prospective clinical studies evaluating cardiac safety in advanced and early-stage HER2-overexpressing breast cancer.

Structured PICO

Does trastuzumab increase the risk of cardiac dysfunction in patients with breast cancer?

P
Population
Patients with advanced or earlier stages of breast cancer overexpressing or amplifying HER2
I
Intervention
Trastuzumab
O
Outcome
Incidence and natural history of trastuzumab-associated cardiac dysfunction (decreases in ejection fraction and congestive heart failure)safety

Trastuzumab therapy in breast cancer patients carries a risk of cardiotoxicity, primarily asymptomatic LVEF decline and occasionally reversible CHF, especially when combined with anthracyclines.

Limitations

  • More data are needed to help elucidate the pathophysiology of this syndrome

Abstract

PURPOSE: This review provides an update on the current understanding of the clinical cardiac tolerability of trastuzumab, a humanized monoclonal antibody effective in the treatment of patients with advanced breast cancer overexpressing or amplifying HER2. METHODS AND RESULTS: We produced a summary of currently available information regarding the incidence and natural history of trastuzumab-associated cardiac dysfunction. Data from new, prospective clinical studies that incorporate close cardiac monitoring and standardized follow-up in patients with either advanced or earlier stages of breast cancer are also presented, and hypotheses regarding potential mechanisms of trastuzumab-related cardiotoxicity are discussed. Patients treated with trastuzumab in the pivotal trials were found to have increased risk for cardiac dysfunction, mostly when used concurrent with anthracyclines. Recent trials have required more stringent and consistent cardiac monitoring criteria and excluded patients with abnormal cardiac function, pre-existing heart disease, and/or high cumulative doses of anthracyclines. Decreases of ejection fraction and a few cases of congestive heart failure (CHF) requiring medical therapy have been detected. Improvements in ejection fraction and the symptoms of CHF have been subsequently noted in a significant number of these patients. CONCLUSION: Trastuzumab is associated with an increased risk of asymptomatic decreases in ejection fraction, and, in a small number of patients, CHF that is almost always responsive to medical management. This risk is greatest in patients receiving concurrent anthracyclines. More data are needed to help elucidate the pathophysiology of this syndrome.

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Cite This Study

Perez et al. (2004) studied this question.

synapsesocial.com/papers/69fbd6c6df6507d4845ddadfhttps://doi.org/10.1200/jco.2004.01.120
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Chemotherapy-Induced Cardiotoxicity: Current Practice and Prospects of Prophylaxis2002 · 201 citations
  2. 2Human Breast Cancer: Correlation of Relapse and Survival with Amplification of the HER-2/ neu Oncogene1987 · 11,806 citations
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  4. 4Differential influence of antiestrogens on the in vitro release of gelatinases (type IV collagenases) by invasive and non-invasive breast cancer cells1997 · 28 citations
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