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Ketoacidosis With Canagliflozin Prescribed for Phosphoinositide 3-Kinase Inhibitor–Induced Hyperglycemia: A Case Report

机译:卡那列净治疗酮症酸中毒为磷酸肌醇3-激酶抑制剂诱导的高血糖症:一例报告

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摘要

Context. Many phosphoinositide-3-kinase (PI3K) inhibitors are under trial for cancer treatment. We present a patient taking taselisib who developed ketoacidosis within 1 week of starting canagliflozin. Case Description. A 69-year-old female patient with no previous history of diabetes mellitus was enrolled in a clinical trial for taselisib therapy in stage IV breast cancer. Hyperglycemia treatment with metformin was insufficient and not tolerated. The addition of canagliflozin daily resulted in ketoacidosis and hospitalization within 1 week. Conclusions. This case report brings together 2 poorly understood and relatively understudied disorders of glucose homeostasis: hyperglycemia due to PI3K inhibition and euglycemic ketoacidosis due to dehydration/SGLT2 inhibition. It demonstrates the complexities of glucose management in the setting of PI3K inhibition. PI3K stimulation (via insulin) in this setting is counterintuitive; therefore, non–insulin-mediated therapies (eg, metformin, thiazolidinediones) might be favored over insulin-mediated therapies.
机译:上下文。许多磷酸肌醇-3-激酶(PI3K)抑制剂正在接受癌症治疗的试验。我们介绍了一位服用taselisib的患者,在开始使用canagliflozin后1周内出现了酮症酸中毒。案例说明。一名没有糖尿病史的69岁女性患者参加了taselisib治疗IV期乳腺癌的临床试验。用二甲双胍治疗高血糖不足,不能耐受。每天添加canagliflozin会导致酮症酸中毒并在1周内住院。结论。该病例报告汇集了2种尚未被了解和相对研究不足的葡萄糖稳态的疾病:由于PI3K抑制而引起的高血糖症和由于脱水/ SGLT2抑制而引起的血糖正常的酮症酸中毒。它证明了在PI3K抑制情况下葡萄糖管理的复杂性。在这种情况下(通过胰岛素)PI3K刺激是违反直觉的;因此,非胰岛素介导的疗法(如二甲双胍,噻唑烷二酮)可能比胰岛素介导的疗法更受青睐。

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