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Trastuzumab-related cardiac events in the treatment of early breast cancer

机译:曲妥珠单抗相关的心脏事件在早期乳腺癌的治疗中

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Trastuzumab is considered a cornerstone in the treatment of human epidermal growth factor receptor-2 (HER2)-positive breast cancer. Cardiac toxicity is an important side effect of treatment and can limit the use of this drug known to act synergistically with cardiotoxicity from anthracyclines. A retrospective study was performed on breast cancer patients with early breast cancer, and HER2 overexpression treated with adjuvanteoadjuvant chemotherapy and trastuzumab between 2005 and 2010. Cardiac events (CE) were recorded if left ventricular ejection fraction (LVEF) reduction was more than 10 % from baseline echocardiography. Treatment-related potential risk and protective factors were recorded. Median age of the 124 patients included in this analysis was 51 years (range 29-70 years). Treatment regimens were anthracycline-cyclophosphamide (AC)-Taxol (105 patients), TCH (12 patients), and CAF/Taxol combination (7 patients). CE were observed in 26 (21 %) patients. Trastuzumab was stopped in 9 (7 %) patients and rechallenged in five after periods ranging from 19 to 120 days. There was a significant decrease in LVEF between baseline/post-AC and during trastuzumab treatment (mean LVEF 64.29 vs. 61.97 %, p < 0.001). Treatment-related risk factors were age and interval since last AC. Trastuzumab loading dose (8 vs. 4 mg) did not influence CE rate. 56 (45 %) patients received left chest wall irradiation with significantly increased CE rates, 16 (31.4 %) versus 10 (15.4 %), in patients without radiotherapy (p < 0.05). The presence of any cardiac risk factor caused a trend toward increased risk, not statistically significant. No connection was found between possible cardioprotective drugs and reduced rates of toxicity. The incidence of cardiac toxicity with trastuzumab adjuvant treatment in our study is similar to other reports. Only radiotherapy to the left chest wall increased the risk for CE. Further prospective studies are needed, including echocardiographic measurement and biochemical data (troponin I), for early recognition and monitoring of high-risk patients.
机译:曲妥珠单抗被认为是治疗人类表皮生长因子受体2(HER2)阳性乳腺癌的基石。心脏毒性是治疗的重要副作用,并且可以限制使用已知与蒽环类药物具有心脏毒性协同作用的药物。对2005年至2010年间乳腺癌的早期乳腺癌患者以及辅助/新辅助化疗和曲妥珠单抗治疗的HER2过表达进行了回顾性研究。如果左室射血分数(LVEF)降低超过10,则记录心脏事件(CE)基线超声心动图的百分比。记录与治疗有关的潜在风险和保护因素。该分析中包括的124位患者的中位年龄为51岁(范围为29-70岁)。治疗方案为蒽环类-环磷酰胺(AC)-紫杉醇(105例),TCH(12例)和CAF / Taxol组合(7例)。在26(21%)位患者中观察到CE。曲妥珠单抗停药9例(占7%),经过19天至120天不等的5个小时后再次发作。在基线/ AC后和曲妥珠单抗治疗期间,LVEF显着降低(LVEF平均为64.29对61.97%,p <0.001)。与治疗相关的危险因素是上次AC以来的年龄和间隔。曲妥珠单抗负荷剂量(8 mg对4 mg)不影响CE发生率。不进行放射治疗的患者中,有56名(45%)接受左胸壁照射,CE率显着提高,分别为16名(31.4%)和10名(15.4%)(p <0.05)。任何心脏危险因素的存在都会导致危险增加的趋势,但无统计学意义。在可能的心脏保护药物与降低的毒性率之间未发现任何联系。本研究中曲妥珠单抗辅助治疗对心脏毒性的发生率与其他报道相似。仅对左胸壁放疗会增加发生CE的风险。需要进行进一步的前瞻性研究,包括超声心动图测量和生化数据(肌钙蛋白I),以早期识别和监测高危患者。

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