Farah Stephanie J, Masri Nohad, Ghanem Hady, Azar Madona
AACE Clin Case Rep. 2020 Sep 24;6(6):e349-e351. doi: 10.4158/ACCR-2020-0452. eCollection 2020 Nov-Dec.
Alpelisib-induced diabetic ketoacidosis (DKA) is a rare, but life-threatening, adverse event. There have been only 2 reported cases in the literature. We describe such a case, with emphasis on the importance of screening and achieving adequate glycemic control prior to and after initiation of therapy.
A 49-year-old woman, known to have advanced breast cancer, presented with a 3-day history of nausea, vomiting, and diffuse abdominal pain. She had started alpelisib at 300 mg/day 2 months prior to presentation, after failing other options. She was diagnosed with DKA using her clinical and laboratory features, leading to treatment with hydration and intravenous insulin therapy.
Laboratory data showed high anion gap metabolic acidosis, hyperglycemia, and ketonemia with negative GAD-65 antibodies, leading to the diagnosis of alpelisib-associated DKA. Alpelisib was held, and she was treated with intravenous insulin and hydration. When DKA and hyperglycemia resolved, alpelisib was resumed at a lower dose (200 mg/day) and her blood glucose was managed using a regimen combining insulin and metformin.
Phosphatidylinositol-3 kinase signaling is important for the metabolic actions of insulin, and alpelisib has been associated with severe hyperglycemia. Metformin is the first-line treatment, however when DKA is the presenting syndrome, insulin needs to be considered. Blood glucose and hemoglobin A should be checked prior to treatment initiation and monitored closely after drug initiation. DKA, albeit rare, must be considered in an acutely ill, alpelisib-treated patients presenting with metabolic acidosis, and if drug discontinuation is not an option, insulin treatment may be required to control glycemia.
阿哌利西布诱发的糖尿病酮症酸中毒(DKA)是一种罕见但危及生命的不良事件。文献中仅报道过2例。我们描述了这样一个病例,重点强调在治疗开始前和开始后进行筛查以及实现充分血糖控制的重要性。
一名49岁的女性,已知患有晚期乳腺癌,出现了3天的恶心、呕吐和弥漫性腹痛病史。在其他治疗方案失败后,她于就诊前2个月开始服用阿哌利西布,剂量为每日300毫克。根据其临床和实验室特征,她被诊断为DKA,随后接受了补液和静脉胰岛素治疗。
实验室数据显示高阴离子间隙代谢性酸中毒、高血糖和酮血症,谷氨酸脱羧酶65抗体阴性,从而诊断为阿哌利西布相关的DKA。停用阿哌利西布,她接受了静脉胰岛素和补液治疗。当DKA和高血糖症状缓解后,以较低剂量(每日200毫克)恢复使用阿哌利西布,并采用胰岛素和二甲双胍联合方案控制她的血糖。
磷脂酰肌醇-3激酶信号传导对胰岛素的代谢作用很重要,阿哌利西布与严重高血糖有关。二甲双胍是一线治疗药物,然而当出现DKA综合征时,则需要考虑使用胰岛素。在治疗开始前应检查血糖和糖化血红蛋白,并在药物开始使用后密切监测。对于患有代谢性酸中毒的急性病、接受阿哌利西布治疗的患者,尽管DKA罕见,但必须予以考虑,如果不能停用药物,则可能需要胰岛素治疗来控制血糖。