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Cardiotoxicity and Cardiac Monitoring During Adjuvant Trastuzumab in Daily Dutch Practice: A Study of the Southeast Netherlands Breast Cancer Consortium

机译:荷兰日常实践中辅助曲妥珠单抗期间的心脏毒性和心脏监测:荷兰东南部乳腺癌协会的一项研究

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Introduction. We assessed the incidence and timing of first cardiac events, impact on trastuzumab prescription, and role of left ventricular ejection fraction (LVEF) monitoring in daily practice of trastuzumab-treated patients with human epidermal growth receptor 2 (HER2)-positive early breast cancer. Methods. We included all patients with stage Ia??III breast cancer diagnosed in the early years (2005a??2007) after the introduction of adjuvant trastuzumab in five hospitals in Southeast Netherlands. We studied the incidence and timing of cardiotoxicity in patients treated with adjuvant trastuzumab, using similar cardiac endpoints as in the Herceptin Adjuvant (HERA) trial. Results. Of 2,684 included patients, 476 (17.7%) had a HER2-positive tumor. Of these, 269 (56.9%) were treated with adjuvant chemotherapy, and of these, 230 (85.5%) also received trastuzumab. Cardiotoxicity was observed in 29 of 230 patients (12.6%). Twenty of the 230 patients (8.7%) had symptomatic cardiotoxicity, defined as a drop in LVEF of at least 10 percentage points and to below 50%, accompanied by symptoms of congestive heart failure. Trastuzumab was definitely discontinued because of supposed cardiotoxicity in 36 patients (15.6%), of whom only 15 (6.5%) had a significant LVEF drop. Of the 36 patients who prematurely discontinued trastuzumab (including the 29 in whom cardiotoxicity was observed), 84.8% stopped in the first 6 months. No cardiac deaths were seen. Conclusion. In the first years after implementation of trastuzumab for treatment of early breast cancer, physicians frequently based their decision to discontinue treatment on patient symptoms apart from LVEF outcome. We suggest that focusing LVEF monitoring on the first 6 months might be more cost-effective without compromising patient safety. Nonetheless, further research is needed. Implications for Practice: Knowledge of when cardiotoxicity occurs in daily practice will help shape the best follow-up method for cardiac monitoring in trastuzumab-treated patients with human epidermal growth receptor 2-positive early breast cancer. In the first years after implementation of trastuzumab for treatment of early breast cancer, physicians frequently based their decision to discontinue treatment on patient symptoms apart from left ventricular ejection fraction (LVEF) outcome. When cardiotoxicity was found in daily practice, it occurred mainly in the first 6 months after start of trastuzumab. This study suggests that focusing LVEF monitoring on the first 6 months might be more cost-effective without compromising patient safety. This insight stresses the relevance of performing real-world analyses.
机译:介绍。我们评估了首次心脏事件的发生率和时机,对曲妥珠单抗处方的影响以及左室射血分数(LVEF)监测在曲妥珠单抗治疗的人表皮生长受体2(HER2)阳性早期乳腺癌患者的日常实践中的作用。方法。我们纳入了在荷兰东南部的五家医院中引入曲妥珠单抗辅助治疗后(2005a-2007年)在早期(2005a-2007年)诊断出的所有Ia-III期乳腺癌患者。我们使用与赫赛汀佐剂(HERA)试验相似的心脏终点研究了接受曲妥珠单抗辅助治疗的患者的心脏毒性发生率和时机。结果。在2,684名患者中,有476名(17.7%)患有HER2阳性肿瘤。其中,有269例(56.9%)接受了辅助化疗,其中230例(85.5%)也接受了曲妥珠单抗治疗。 230名患者中有29名(12.6%)出现心脏毒性。 230名患者中有20名(8.7%)有症状性心脏毒性,定义为LVEF下降至少10个百分点至50%以下,并伴有充血性心力衰竭症状。曲妥珠单抗肯定因36名患者(15.6%)的心脏毒性而终止使用,其中只有15名(6.5%)的LVEF明显降低。在36例过早停用曲妥珠单抗的患者中(包括29例观察到心脏毒性的患者),有84.8%的患者在头6个月内停止了治疗。未见心脏死亡。结论。在将曲妥珠单抗用于早期乳腺癌的治疗后的头几年,医生通常根据患者的症状(LVEF结果除外)决定停止治疗。我们建议在不影响患者安全的情况下,将LVEF监测重点放在头6个月可能更具成本效益。尽管如此,仍需要进一步的研究。实践的意义:日常实践中何时发生心脏毒性的知识将有助于制定最佳的随访方法,用于接受曲妥珠单抗治疗的人表皮生长受体2阳性的早期乳腺癌患者的心脏监测。在将曲妥珠单抗用于早期乳腺癌的治疗后的头几年,医生经常根据他们的决定(除左心室射血分数(LVEF)结果以外)根据患者症状中止治疗。在日常实践中发现心脏毒性时,主要发生在曲妥珠单抗开始后的前6个月。这项研究表明,在不影响患者安全的前提下,将LVEF监测重点放在头6个月可能更具成本效益。这种见解强调了执行真实世界分析的相关性。

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