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October 28, 2005Journal of Clinical Oncology816 citations

Assessment of Cardiac Dysfunction in a Randomized Trial Comparing Doxorubicin and Cyclophosphamide Followed by Paclitaxel, With or Without Trastuzumab As Adjuvant Therapy in Node-Positive, Human Epidermal Growth Factor Receptor 2–Overexpressing Breast Cancer: NSABP B-31

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ETElizabeth Tan-ChiuGYGreg YothersEREdward H. Romond

Structured PICO

Does adding trastuzumab to paclitaxel after doxorubicin and cyclophosphamide increase the risk of cardiac events in patients with node-positive, HER2-positive breast cancer?

P
Population
1,664 patients with node-positive, HER2-positive breast cancer and normal post-AC left ventricular ejection fraction
I
Intervention
Doxorubicin and cyclophosphamide (AC) followed by paclitaxel plus 52 weeks of trastuzumab beginning concurrently with paclitaxel
C
Comparator
Doxorubicin and cyclophosphamide (AC) followed by paclitaxel
O
Outcome
Cardiac event (CE), defined as New York Heart Association class III or IV congestive heart failure or possible/probable cardiac deathsafety

The addition of trastuzumab to paclitaxel after anthracycline therapy in HER2-positive breast cancer significantly increases the risk of congestive heart failure and cardiac dysfunction.

Abstract

PURPOSE: Trastuzumab is effective in treating human epidermal growth factor receptor 2 (HER2) -positive breast cancer, but it increases frequency of cardiac dysfunction (CD) when used with or after anthracyclines. PATIENTS AND METHODS: National Surgical Adjuvant Breast and Bowel Project trial B-31 compared doxorubicin and cyclophosphamide (AC) followed by paclitaxel with AC followed by paclitaxel plus 52 weeks of trastuzumab beginning concurrently with paclitaxel in patients with node-positive, HER2-positive breast cancer. Initiation of trastuzumab required normal post-AC left ventricular ejection fraction (LVEF) on multiple-gated acquisition scan. If symptoms suggestive of congestive heart failure (CHF) developed, source documents were blindly reviewed by an independent panel of cardiologists to determine whether criteria were met for a cardiac event (CE), which was defined as New York Heart Association class III or IV CHF or possible/probable cardiac death. Frequencies of CEs were compared between arms. RESULTS: Among patients with normal post-AC LVEF who began post-AC treatment, five of 814 control patients subsequently had confirmed CEs (four CHFs and one cardiac death) compared with 31 of 850 trastuzumab-treated patients (31 CHFs and no cardiac deaths). The difference in cumulative incidence at 3 years was 3.3% (4.1% for trastuzumab-treated patients minus 0.8% for control patients; 95% CI, 1.7% to 4.9%). Twenty-seven of the 31 patients in the trastuzumab arm have been followed for > or = 6 months after diagnosis of a CE; 26 were asymptomatic at last assessment, and 18 remained on cardiac medication. CHFs were more frequent in older patients and patients with marginal post-AC LVEF. Fourteen percent of patients discontinued trastuzumab because of asymptomatic decreases in LVEF; 4% discontinued trastuzumab because of symptomatic cardiotoxicity. CONCLUSION: Administering trastuzumab with paclitaxel after AC increases incidence of CHF and lesser CD. Potential cardiotoxicity should be carefully considered when discussing benefits and risks of this therapy.

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Cite This Study

Tan-Chiu et al. (2005) studied this question.

synapsesocial.com/papers/69fbd6c6df6507d4845ddadehttps://doi.org/10.1200/jco.2005.02.4091
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