Ribociclib-Induced hepatotoxicity exacerbated by fenugreek supplement use: A case report.

IF 0.9 4区 医学 Q4 ONCOLOGY
Journal of Oncology Pharmacy Practice Pub Date : 2025-09-01 Epub Date: 2025-05-19 DOI:10.1177/10781552251340911
Yousra Al Harrak, Sihame Lkhoyaali, Oumaima Lamsyah, Marie Monique Tine, Hafsa Bechar, Ghita Benabdallah, Houda Sefiani, Saber Boutayeb, Hassan Errihani
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引用次数: 0

Abstract

BackgroundCyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors, such as ribociclib, are the cornerstone of treatment for estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer. However, ribociclib is known to cause hepatotoxicity, and the role of other dietary supplements in this process is not well understood.Case PresentationA 47-year-old woman with metastatic breast cancer experienced grade III hepatotoxicity shortly after starting ribociclib. Despite discontinuing the drug, transaminase levels remained elevated. Using the the Roussel Uclaf Causality Assessment Method (RUCAM), a probable drug-induced liver injury was identified (score: 6). Upon disclosure of concurrent use of a fenugreek-based supplement, the revised RUCAM score dropped to 4. Further anamnesis revealed concurrent intake of a fenugreek-based supplement, prompting a revised RUCAM score of 4. The Naranjo Adverse Drug Reaction Probability Scale also indicated a possible association (score: 4). In contrast, the Drug Interaction Probability Scale (DIPS) scored 5, suggesting a probable herb-drug interaction between ribociclib and fenugreek.Management and OutcomeTransaminase levels gradually returned to normal within eight weeks of stopping ribociclib and four weeks after discontinuing the fenugreek supplement. The patient was counseled to avoid herbal supplements and initiated on palbociclib as an alternative CDK4/6 inhibitor. Liver function remained stable with no recurrent hepatotoxicity.DiscussionFenugreek modulates CYP3A4, which metabolizes ribociclib. This case highlights underrecognized herb-drug interactions in oncology.

使用胡芦巴补充剂加重了核糖素诱导的肝毒性:1例报告。
细胞周期蛋白依赖性激酶4和6 (CDK4/6)抑制剂,如ribociclib,是雌激素受体阳性(ER+),人表皮生长因子受体2阴性(HER2-)转移性乳腺癌治疗的基础。然而,已知核糖环尼可引起肝毒性,其他膳食补充剂在这一过程中的作用尚不清楚。病例介绍:一名47岁女性转移性乳腺癌患者在开始使用核糖环尼后不久出现III级肝毒性。尽管停药,转氨酶水平仍然升高。采用Roussel - Uclaf因果关系评估法(RUCAM),确定可能的药物性肝损伤(得分:6分)。同时使用葫芦巴补充剂后,修订后的RUCAM评分降至4分。进一步的记忆显示同时摄入葫芦巴为基础的补充剂,促使修订RUCAM评分为4。Naranjo药物不良反应概率量表也显示可能存在关联(得分:4)。相比之下,药物相互作用概率量表(DIPS)得分为5分,表明核糖环尼和胡芦巴之间可能存在草药相互作用。转氨酶水平在停用核糖环尼8周和停用胡芦巴补充剂4周内逐渐恢复正常。建议患者避免服用草药补充剂,并开始使用帕博西尼作为替代的CDK4/6抑制剂。肝功能保持稳定,无肝毒性复发。葫芦巴调节代谢核糖环尼的CYP3A4。这个病例突出了肿瘤中未被充分认识的草药相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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