Cancer Therapy–Related Cardiac Dysfunction in Patients With Prostate Cancer Undergoing Androgen Deprivation Therapy

Author:

Chen Dong‐Yi12ORCID,Lee Cheng‐Hung12,Tsai Ming‐Lung32,Hsieh Ming‐Jer12ORCID,Chuang Cheng‐Keng4ORCID,Pang See‐Tong4,Chen Shao‐Wei256ORCID,Tseng Chi‐Nan25ORCID,Chang Shang‐Hung1,Chu Pao‐Hsien12ORCID,Hsieh I‐Chang12,Wu Victor Chien‐Chia12ORCID,Huang Wen‐Kuan27ORCID

Affiliation:

1. Division of Cardiology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou Chang Gung University College of Medicine Taoyuan Taiwan

2. Chang Gung University College of Medicine Taoyuan Taiwan

3. Division of Cardiology New Taipei Municipal TuCheng Hospital New Taipei City Taiwan

4. Division of Urology, Department of Surgery, Chang Gung Memorial Hospital at Linkou Chang Gung University College of Medicine Taoyuan Taiwan

5. Department of Thoracic and Cardiovascular Surgery Chang Gung Memorial Hospital at Linkou Taoyuan Taiwan

6. Center for Big Data Analytics and Statistics, Department of Medical Research and Development, Chang Gung Memorial Hospital at Linkou Taoyuan Taiwan

7. Division of Hematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou Chang Gung University College of Medicine Taoyuan Taiwan

Abstract

Background The risk of cardiac dysfunction for patients with prostate cancer undergoing androgen deprivation therapy (ADT) in the real‐world setting remains unclear. Methods and Results A total of 1120 patients with prostate cancer and a baseline echocardiography scan were identified from Chang Gung Research Database between January 1, 2001 and December 31, 2019. Patients were treated with gonadotropin‐releasing hormone agonist therapy, gonadotropin‐releasing hormone antagonist therapy, or bilateral orchiectomy. Changes in left ventricular ejection fraction (LVEF) were further assessed in 421 patients using repeated measurements of LVEF before and during ADT treatment. The incidence of cancer therapy–related cardiac dysfunction (CT‐RCD) was evaluated and defined as a ≥10% absolute decline in LVEF from baseline to a value of <53%. Among 421 patients undergoing ADT, LVEF declined from 66.3±11.3% to 62.5±13.6% (95% CI of mean difference: −5.0% to −2.7%) after a mean follow‐up period of 1.6±0.8 years. CT‐RCD occurred in 58 patients (13.7%) with a nadir LVEF of 40.3±9.1% after ADT. Lower baseline LVEF was significantly associated with CT‐RCD (odds ratio, 1.07 [95% CI, 1.04–1.10]). The area under the curve of baseline LVEF for discriminating CT‐RCD was 75.6%, with the corresponding optimal cutoff value of 64.5% (sensitivity, 79.3%; specificity, 67.2%). Conclusions ADT with gonadotropin‐releasing hormone agonist therapy, gonadotropin‐releasing hormone antagonist therapy, and bilateral orchiectomy were associated with an increased risk of CT‐RCD in patients with prostate cancer. In addition, lower baseline LVEF was a significant predictor of CT‐RCD in patients with prostate cancer undergoing treatment with ADT.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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