Alam Salma, Illo Chidi, Ma Yuk Ting, Punia Pankaj
Queen Elizabeth Hospital, Birmingham, United Kingdom.
School of Cancer Sciences, University of Birmingham, Birmingham, United Kingdom.
Case Rep Oncol. 2018 Apr 5;11(1):221-227. doi: 10.1159/000488139. eCollection 2018 Jan-Apr.
Gemcitabine is not considered a cardiotoxic agent generally; so far only very few case reports have been reported in the literature on different aspects of cardiac side effects. Here we report a case series of 3 patients who developed congestive cardiac failure, when treated with gemcitabine monotherapy in the adjuvant setting for pancreatic cancers. Adjuvant chemotherapy with gemcitabine has been the standard of care for pancreatic cancer patients after successful surgery since the results of the CONKO-001 and ESPAC3 study were published. Gemcitabine was administered on days 1, 8, and 15 of a 28-day cycle at 1,000 mg/m. All 3 patients developed symptoms suggestive of cardiac failure with a drop in ejection fraction on echocardiography, and responded to conservative treatment for heart failure after withdrawal of gemcitabine therapy. Early withdrawal of gemcitabine chemotherapy is recommended in addition to a need for studies required to evaluate the mechanism of cardiotoxicity. As per available literature, patients with diabetes and having received a total dose greater than 15,000 mg/m are generally at a higher risk and require close surveillance.
一般认为吉西他滨不是一种心脏毒性药物;到目前为止,文献中仅报道了极少数关于心脏副作用不同方面的病例报告。在此,我们报告一组3例患者的病例系列,这些患者在辅助治疗胰腺癌时接受吉西他滨单药治疗后出现了充血性心力衰竭。自CONKO - 001和ESPAC3研究结果发表以来,吉西他滨辅助化疗一直是胰腺癌患者成功手术后的标准治疗方法。吉西他滨在28天周期的第1、8和15天给药,剂量为1000mg/m²。所有3例患者均出现提示心力衰竭的症状,超声心动图显示射血分数下降,在停用吉西他滨治疗后对心力衰竭的保守治疗有反应。除了需要进行评估心脏毒性机制的研究外,建议早期停用吉西他滨化疗。根据现有文献,糖尿病患者且接受的总剂量大于15000mg/m²通常风险较高,需要密切监测。