Decline in Left Ventricular Ejection Fraction Following Anthracyclines Predicts Trastuzumab Cardiotoxicity

被引:33
作者
Goel, Shorn [1 ,2 ,3 ,4 ]
Liu, Jia [2 ]
Guo, Hao [1 ]
Barry, William [1 ]
Bell, Richard [5 ]
Murray, Bronwyn [2 ]
Lynch, Jodi [6 ,7 ]
Bastick, Patricia [6 ]
Chantrill, Lorraine [8 ]
Kiely, Belinda E. [9 ]
Abdi, Ehtesham [10 ,11 ]
Rutovitz, Josie [12 ]
Asghari, Ray [13 ]
Sullivan, Anne [9 ]
Harrison, Michelle [2 ]
Kohonen-Corish, Maija [14 ]
Beith, Jane [2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Chris OBrien Lifehouse, Dept Med Oncol, Sydney, NSW, Australia
[3] Peter MacCallum Canc Ctr, 305 Grattan St, Melbourne, Vic 3124, Australia
[4] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic, Australia
[5] Andrew Love Canc Ctr, Barwon Hlth Canc Serv, Geelong, Vic, Australia
[6] St George Hosp, St George Canc Care Ctr, Sydney, NSW, Australia
[7] Sutherland Hosp, Dept Med Oncol, Sydney, NSW, Australia
[8] Liverpool Hosp, Macarthur Canc Therapy Ctr, Sydney, NSW, Australia
[9] Concord Repatriat Gen Hosp, Concord Canc Ctr, Sydney, NSW, Australia
[10] Tweed Hosp, Tweed Heads, Australia
[11] Griffith Univ, Gold Coast, Australia
[12] San Integrated Canc Ctr, Northern Haematol & Oncol Grp, Sydney, NSW, Australia
[13] Bankstown Hosp, Bankstown Canc Ctr, Sydney, NSW, Australia
[14] Garvan Inst Med Res, Kinghorn Canc Ctr, Sydney, NSW, Australia
关键词
biomarkers; breast cancer; cardiotoxicity; supportive care; trastuzumab; EARLY BREAST-CANCER; CARDIAC TOXICITY; HERCEPTIN ADJUVANT; PLUS TRASTUZUMAB; HER2; BIOMARKERS; THERAPY; DOXORUBICIN; PACLITAXEL; SAFETY;
D O I
10.1016/j.jchf.2019.04.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The aim of CATS (Cardiotoxicity of Adjuvant Trastuzumab Study) was to prospectively assess clinical, biochemical, and genomic predictors of trastuzumab-related cardiotoxicity (TRC). BACKGROUND Cardiac dysfunction is a common adverse effect of trastuzumab. Studies to identify predictive biomarkers for TRC have enrolled heterogeneous populations and yielded mixed results. METHODS A total of 222 patients with early-stage human epidermal growth factor receptor 2-positive breast cancer scheduled to receive adjuvant anthracyclines followed by 12 months of trastuzumab were prospectively recruited from 17 centers. Left ventricular ejection fraction (LVEF), troponin T, and N-terminal prohormone of brain natriuretic peptide were measured at baseline, post-anthracycline, and every 3 months during trastuzumab. Germline single-nucleotide polymorphisms in ERBB2, FCGR2A, and FCGR3A were analyzed. TRC was defined as symptomatic heart failure; cardiac death, arrhythmia, or infarction; a decrease in LVEF of > 15% from baseline; or a decrease in LVEF of > 10% to < 50%. RESULTS TRC occurred in 18 of 217 subjects (8.3%). Lower pre-anthracycline LVEF and greater interval decline in LVEF from pre- to post-anthracycline were each associated with TRC on multivariate analyses (odds ratio: 3.9 [p = 0.0001] and 7.9 [p < 0.0001] for a 5% absolute change in LVEF). Higher post-anthracycline N-terminal prohormone of brain natriuretic peptide level was associated with TRC on univariate but not multivariate analyses. There were no associations between troponin T or ERBB2/FGCR polymorphisms and TRC. Baseline LVEF and LVEF change post-anthracycline were used to generate a "low-risk TRC score" to identify patients with low TRC incidence. CONCLUSIONS Low baseline LVEF and greater LVEF decline post-anthracycline were both independent predictors of TRC. The other biomarkers did not further improve the ability to predict TRC. (Cardiotoxicity of Adjuvant Trastuzumab [CATS]; NCT00858039) (C) 2019 by the American College of Cardiology Foundation.
引用
收藏
页码:795 / 804
页数:10
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