Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, Jiangsu, China.
BMC Pulm Med. 2020 Jun 24;20(1):181. doi: 10.1186/s12890-020-01217-4.
Torsade de pointes (TdP) is a malignant arrhythmia that can be induced by QT internal prolongation due to a variety of factors. Here we report an elderly patient with advanced non-small cell lung cancer (NSCLC) had sudden TdP during hospitalization, which was caused by multiple factors such as osimertinib, moxifloxacin and patient self-factors.
An 85-year-old man with advanced NSCLC with brain andbone metastasis was initially treated with gefitinib targeted therapy. After 4 months treatment, the patient developed drug resistance and a second genetic testing revealed that the T790M mutation was positive. And the patient was then changed to targeted therapy with osimertinib, followed by adverse reactions of varying severity such as diarrhea, electrolyte imbalance, decreased cardiac function, leukopenia, and prolonged QTc interval. Six months after the administration of osimertinib, the patient was admitted to the hospital, chest CT showed the lesion progressed again, and during which hospital-acquired infection occurred. After concomitant use of moxifloxacin, the patient had sudden TdP, and finally died of this cardiac event.
It is suggested that clinicians need to identify patients with high risk factors of TdP, and consider comprehensively in concomitant medication to avoid such events to the greatest extent.
尖端扭转型室性心动过速(TdP)是一种恶性心律失常,可由多种因素引起的 QT 间期延长导致。本文报告了一例晚期非小细胞肺癌(NSCLC)老年患者,在住院期间突发 TdP,其发生与奥希替尼、莫西沙星以及患者自身等多种因素有关。
一名 85 岁男性,患有晚期 NSCLC 伴脑和骨转移,最初接受吉非替尼靶向治疗。治疗 4 个月后,患者出现耐药,第二次基因检测显示 T790M 突变阳性。随后,患者改用奥希替尼进行靶向治疗,随后出现不同严重程度的不良反应,如腹泻、电解质失衡、心功能下降、白细胞减少和 QTc 间期延长。奥希替尼治疗 6 个月后,患者因病情进展再次住院,期间发生医院获得性感染。在合用莫西沙星后,患者突发 TdP,最终死于该心脏事件。
建议临床医生需要识别 TdP 的高危患者,并在联合用药时全面考虑,以最大程度避免此类事件的发生。