Cardiotoxicity in breast cancer patients receiving trastuzumab with or without prior anthracycline-based chemotherapy: A prospective study from a tertiary cancer institute at Guwahati, India

A. Ray, N. Kalita, N. Mahanta, A. Ali, Madhav Kashyap
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Abstract

Background: Trastuzumab (Herceptin) is used in human epidermal growth factor receptor-2 (HER2)-positive breast cancer patients either alone or in combination with various chemotherapeutic agents in the neoadjuvant, adjuvant as well as palliative settings. Cardiotoxicity remains an issue of concern with the use of trastuzumab which may be enhanced with the prior use of anthracycline-based chemotherapeutic agents. Aim: This prospective study was conducted with the aim of identifying the occurrence of cardiotoxicity in patients receiving trastuzumab with or without a history of prior use of anthracycline-based chemotherapy. Materials and Methods: The study was conducted over a period of 1½ years. All the HER2-positive breast cancer patients who received trastuzumab-based therapy in adjuvant as well as maintenance settings and the cardiotoxicity in terms of drop in left ventricular ejection fraction (LVEF) from the lower limit of normal range were evaluated. A significant drop is defined when LVEF drop is >10%. Cardiotoxicity was compared between those who received prior anthracycline-based chemotherapy versus nonanthracycline-based chemotherapy. Results: A total of 62 HER2-positive breast cancer patients who fulfilled the inclusion and exclusion criteria were enrolled for analysis. Thirty-two patients received prior anthracycline-based chemotherapy and 30 patients received nonanthracycline-based chemotherapy. A significant drop in LVEF of >10% was found in 20 out of 62 patients (32.3%). This significant drop in LVEF was found more in those patients who received prior anthracycline-based chemotherapy (n = 15) versus who did not receive prior anthracycline-based chemotherapy (n = 5) (46.9% vs. 16.7%; P = 0.0109). Conclusion: Trastuzumab-induced cardiotoxicity (LVEF drop >10%) is higher among breast cancer patients who received prior anthracycline-based chemotherapy as compared to those who did not receive prior anthracycline. This clinically significant drop in LVEF warranted an interruption in the treatment till stabilization and improvement of the cardiac function.
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接受曲妥珠单抗合并或未接受蒽环类药物化疗的乳腺癌患者的心脏毒性:来自印度Guwahati三级癌症研究所的一项前瞻性研究
背景:曲妥珠单抗(赫赛汀)用于人表皮生长因子受体2 (HER2)阳性乳腺癌患者,可单独使用或与各种化疗药物联合使用,用于新辅助、辅助和姑息治疗。心脏毒性仍然是使用曲妥珠单抗的一个值得关注的问题,这可能会因先前使用蒽环类化疗药物而增强。目的:这项前瞻性研究的目的是确定接受曲妥珠单抗治疗的患者是否有蒽环类药物化疗史。材料与方法:本研究历时1年半。所有接受以曲妥珠单抗为基础的辅助和维持治疗的her2阳性乳腺癌患者以及左心室射血分数(LVEF)从正常范围下限下降的心脏毒性进行了评估。当LVEF下降>10%时为显著下降。比较先前接受蒽环类药物化疗与非蒽环类药物化疗的患者的心脏毒性。结果:共纳入62例符合纳入和排除标准的her2阳性乳腺癌患者进行分析。32例患者先前接受了蒽环类药物化疗,30例患者接受了非蒽环类药物化疗。62例患者中有20例(32.3%)LVEF显著下降>10%。先前接受过蒽环类药物化疗的患者(n = 15)与未接受蒽环类药物化疗的患者(n = 5)相比,LVEF的显著下降更为明显(46.9% vs. 16.7%;P = 0.0109)。结论:曲妥珠单抗诱导的心脏毒性(LVEF下降>10%)在先前接受过蒽环类药物化疗的乳腺癌患者中高于先前未接受蒽环类药物化疗的患者。这种临床上显著的LVEF下降需要中断治疗,直到心功能稳定和改善。
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