Real-world data of cardiotoxicity during long-term therapy with trastuzumab in human epidermal growth factor receptor-2-positive metastatic breast cancer

Author:

Iljovska Marina1,Lazareva Emilija1,Smichkoska Snezhana1,Klisarovska Violeta2,Stojkovski Igor3,Petkovska Gordana1,Mitreski Nenad4

Affiliation:

1. University Clinic for Radiotherapy and Oncology, Department of Breast and Thorax Malignancies, Skopje, North Macedonia + Ss. Cyril and Methodius University, Faculty of Medicine, Skopje, North Macedonia

2. Ss. Cyril and Methodius University, Faculty of Medicine, Skopje, North Macedonia + University Clinic for Radiotherapy and Oncology, Department of Gynecologic Oncology and Brachytherapy, Skopje, North Macedonia

3. Ss. Cyril and Methodius University, Faculty of Medicine, Skopje, North Macedonia + University Clinic for Radiotherapy and Oncology, Department of CNS, Bone Tumors and Skin Cancer, Skopje, North Macedonia;

4. Ss. Cyril and Methodius University, Faculty of Medicine, Skopje, North Macedonia + University Clinic for Radiotherapy and Oncology, Department of Gastrointestinal Malignancies, Skopje, North Macedonia

Abstract

Introduction/Objective. This study aims to investigate the cardiotoxicity of long-term therapy with trastuzumab in patients with HER-2-positive metastatic breast cancer. Methods. A total of 48 patients with metastatic HER-2-positive breast cancer were analyzed. The patients received long-term trastuzumab (time of application was longer than 20 months). The analyzed characteristics of the patients were the following: age, initial stage of the disease, application of anti-HER-2 therapy and anthracyclines in the adjuvant setting, the number and type of applied systemic therapies concomitant with trastuzumab in the metastatic setting. Cardiac toxicity was assessed using left ventricular ejection fraction (LVEF) values at three time-points: at the beginning, in the middle, and at the end of treatment period for each patient separately. Results. In 17 (35.4%) patients the trastuzumab treatment was temporary discontinued. The average time of trastuzumab therapy interval was 52.2 ? 23.5 months. The mean LVEF values were 66.73 ? 7.02%, 64.62 ? 5.7%, and 63.44 ? 6.1%, respectively. The mean values of LVEF differed significantly in the three observed time-points (F = 4.9 p = 0.009). Post hoc pairwise comparison, using Bonferroni correction, confirmed significantly lower mean LVEF values at the end point (at the end of treatment) compared with the mean LVEF values at the beginning of anti-HER-2 treatment (p = 0.019), but within the reference range of LVEF ? 50%. Conclusion. The data confirm good safety profile of long-term trastuzumab therapy in HER-2 positive metastatic breast cancer patients considering cardiotoxicity.

Publisher

National Library of Serbia

Subject

General Medicine

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