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在甲状腺乳头状癌中,使用酪氨酸激酶抑制剂联合治疗 26 个月后发生致命性心力衰竭。

Fatal heart failure after a 26-month combination of tyrosine kinase inhibitors in a papillary thyroid cancer.

机构信息

Department of Nuclear Medicine, APHP-Saint-Louis Hospital, Paris, France.

出版信息

Thyroid. 2011 Apr;21(4):451-4. doi: 10.1089/thy.2010.0270. Epub 2011 Mar 8.

Abstract

BACKGROUND

Patients with progressive refractory thyroid cancer are potential candidates for clinical trials using tyrosine kinase inhibitors (TKIs), and a promising proportion of patients in these trials have achieved stable disease. Here we report an unusual adverse experience in a patient receiving a combination of TKIs.

SUMMARY

The patient was a 62-year-old man with chronic myloid leukemia (CML) and thyroid carcinoma that did not concentrate iodide and had metastases. He was started on imatinib for his CML. About 5 months later he was started on sorafenib for his thyroid cancer. At this time he had no risk factors for cardiac disease except moderate obesity. He had a complete cytogenetic response in his CML, and a partial response in his thyroid cancer. Twenty-one months after starting the combination of TKIs, he manifested signs of coronary artery disease. He received a combination of medications and his TKIs were continued. He died of a sudden myocardial infarction with cardiogenic shock 28 months after starting the combination of TKIs. A retrospective analysis of sequential 18-fludeoxyglucose positron emission tomography scans (18-FDG PET scans) were indicative of cardiac toxicity developing during the period of concomitant administration of TKIs.

CONCLUSION

We report the first case of apparent lethal cardiotoxicity with imatinib-sorafenib combined therapy. Combination TKI treatment may enhance the risk of adverse effects. Our experience with this patient suggests that cardiac PET scan should be monitored closely in these type of patients.

摘要

背景

患有进行性难治性甲状腺癌的患者是使用酪氨酸激酶抑制剂 (TKI) 进行临床试验的潜在候选者,这些试验中的相当一部分患者已实现疾病稳定。在这里,我们报告了一名接受 TKI 联合治疗的患者出现的不常见不良事件。

摘要

患者为 62 岁男性,患有慢性髓性白血病 (CML) 和甲状腺癌,后者不能摄取碘且发生转移。他因 CML 开始服用伊马替尼。大约 5 个月后,他开始服用索拉非尼治疗甲状腺癌。此时,他除了中度肥胖外,没有心脏病的危险因素。他的 CML 完全细胞遗传学反应,甲状腺癌部分缓解。开始联合使用 TKI 21 个月后,他出现了冠心病的迹象。他接受了联合药物治疗,继续使用 TKI。开始联合使用 TKI 28 个月后,他因心肌梗塞合并心源性休克突然死亡。对连续 18 氟脱氧葡萄糖正电子发射断层扫描 (18-FDG PET 扫描) 的回顾性分析表明,在同时使用 TKI 期间发生了心脏毒性。

结论

我们报告了首例伊马替尼-索拉非尼联合治疗明显致命性心脏毒性的病例。联合 TKI 治疗可能会增加不良反应的风险。我们对该患者的经验表明,应密切监测此类患者的心脏 PET 扫描。

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