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伊曲康唑增强了一名霍奇金淋巴瘤患者的化疗毒性。

Itraconazole-enhanced chemotherapy toxicity in a patient with Hodgkin lymphoma.

作者信息

Bashir Hamid, Motl Susannah, Metzger Monika L, Howard Scott C, Kaste Sue, Krasin Matthew P, Hudson Melissa M

机构信息

Department of Internal Medicine, University of Tennessee Health Science Center, Memphis, 38105, USA.

出版信息

J Pediatr Hematol Oncol. 2006 Jan;28(1):33-5.

Abstract

The authors describe the clinical course of a boy with Hodgkin lymphoma who developed severe myelosuppression and neurotoxicity after the concurrent administration of vinblastine, doxorubicin, methotrexate, and prednisone chemotherapy (VAMP) and itraconazole. Several case reports have identified itraconazole-enhanced chemotherapy toxicity, especially in association with vinca alkaloid chemotherapy. This patient showed similar exacerbation of chemotherapy toxicity related to concurrent administration of itraconazole and vinblastine, doxorubicin, and methotrexate. Inpatient supportive management along with withdrawal of offending drugs resulted in the resolution of myelotoxic and neurotoxic manifestations. Hepatic cytochrome P450 enzyme inhibition and P-glycoprotein pump inhibitors are believed to interfere with the metabolism of several anticancer agents. Appropriate care should be exercised when combining cancer chemotherapy with cytochrome P450 and P-glycoprotein inhibitors, such as itraconazole.

摘要

作者描述了一名患有霍奇金淋巴瘤的男孩的临床病程,该男孩在同时接受长春碱、阿霉素、甲氨蝶呤和泼尼松化疗(VAMP)及伊曲康唑治疗后出现了严重的骨髓抑制和神经毒性。几例病例报告已证实伊曲康唑会增强化疗毒性,尤其是与长春花生物碱化疗联合使用时。该患者在同时使用伊曲康唑与长春碱、阿霉素和甲氨蝶呤后,也出现了类似的化疗毒性加重情况。住院支持治疗并停用相关药物后,骨髓毒性和神经毒性表现得以缓解。肝细胞色素P450酶抑制和P-糖蛋白泵抑制剂被认为会干扰几种抗癌药物的代谢。在将癌症化疗与细胞色素P450和P-糖蛋白抑制剂(如伊曲康唑)联合使用时,应谨慎处理。

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