Wong Siu-Fun, Jakowatz James G, Taheri Reza
Western University College of Pharmacy, Pomona, CA, USA.
Ann Pharmacother. 2004 Oct;38(10):1655-9. doi: 10.1345/aph.1D546. Epub 2004 Aug 10.
To describe 3 cases of hypertriglyceridemia associated with the use of interferon alfa (IFN-alpha) for the treatment of malignant melanoma and propose a management plan for dyslipidemia associated with interferon therapy.
Three case reports of hypertriglyceridemia with or without elevation of total cholesterol level associated with the use of adjuvant IFN-alpha for the treatment of malignant melanoma are described. These patients received IFN-alpha-based adjuvant therapy with doses ranging from 5-20 million units/m(2) for 1-2 years' duration. The onset and severity of dyslipidemia appeared to occur randomly. Pre-existing cardiovascular disorders did not seem to play a role. The patients were treated with atorvastatin, gemfibrozil, and a combination of lovastatin with niacin, depending on their lipid panel results.
Based on our case reports and published data, hypertriglyceridemia is more frequently associated with longer duration of interferon therapy, although the time of onset is not clearly defined. Presence or absence of baseline dyslipidemia does not seem to play a role in the development of hypertriglyceridemia associated with interferon, and its occurrence and severity are not dependent on the dose. Lifestyle modifications should be encouraged in patients who develop dyslipidemia, and drug treatment should be considered. If drug therapy is indicated, fibric acid derivatives should be considered as first-line therapy. Even at lower doses, this class of drug seems to be effective in managing severe triglyceride elevations in these patients. The Naranjo probability scale of these cases ranged from possible to probable.
Hypertriglyceridemia is a rare but potentially severe adverse consequence of interferon therapy. Patients with malignant melanoma who develop dyslipidemia while receiving interferon should be considered for antidyslipidemic management.
描述3例使用干扰素α(IFN-α)治疗恶性黑色素瘤相关的高甘油三酯血症病例,并提出针对干扰素治疗相关血脂异常的管理方案。
描述了3例使用辅助性IFN-α治疗恶性黑色素瘤相关的高甘油三酯血症病例,总胆固醇水平有或无升高。这些患者接受了基于IFN-α的辅助治疗,剂量为500 - 2000万单位/m²,持续1 - 2年。血脂异常的发作和严重程度似乎是随机发生的。既往心血管疾病似乎未起作用。根据血脂检测结果,患者分别接受阿托伐他汀、吉非贝齐以及洛伐他汀与烟酸的联合治疗。
根据我们的病例报告和已发表的数据,高甘油三酯血症更常与干扰素治疗时间延长相关,尽管发病时间尚无明确界定。基线血脂异常的存在与否似乎对与干扰素相关的高甘油三酯血症的发生没有影响,其发生和严重程度也不依赖于剂量。对于发生血脂异常的患者,应鼓励其改变生活方式,并考虑药物治疗。如果需要药物治疗,应考虑将纤维酸衍生物作为一线治疗药物。即使在较低剂量下,这类药物似乎也能有效控制这些患者严重的甘油三酯升高。这些病例的Naranjo概率量表评分为“可能”到“很可能”。
高甘油三酯血症是干扰素治疗罕见但潜在严重的不良后果。接受干扰素治疗的恶性黑色素瘤患者若发生血脂异常,应考虑进行抗血脂异常管理。