Sahakian Nicolas, Cattieuw Lauranne, Ramillon-Cury Clotilde, Corroller Audrey Bégu-Le, Silvestre-Aillaud Pascale, Béliard Sophie, Valéro René
Department of Nutrition, Metabolic Diseases and Endocrinology, University Hospital La Conception, 147 boulevard Baille, 13005, Marseille, France.
Aix Marseille Univ, APHM, INSERM, INRAE, C2VN, 27 boulevard Jean Moulin, 13005, Marseille, France.
Clin Diabetes Endocrinol. 2021 Jul 20;7(1):17. doi: 10.1186/s40842-021-00125-8.
Hyperglycemia is the most common side-effect of phosphatidylinositol 3-kinase (PI3K) inhibitors that are approved for the treatment of some advanced or metastatic breast cancers. This side-effect is likely due to the central role of PI3K in insulin signalling. Here we report the use of a sodium-glucose cotransporter 2 (SGLT2) inhibitor to manage severe hyperglycemia.
We describe a 74-year-old woman who developed severe uncontrolled hyperglycemia after commencing alpelisib, a new oral PI3K inhibitor indicated for a metastatic breast cancer, despite taking oral anti-diabetic drugs, metformin and vildagliptin, combined with intravenous insulin infusion of up to 250 units/day. The introduction of the SGLT2 inhibitor dapagliflozin rapidly improved blood glucose with a drastic reduction in insulin dosage, from 250 to 12 units/day, and without significant side-effects.
We report the successful management of hyperglycemia induced by alpelisib using a SGLT2 inhibitor without the need to discontinue effective cancer treatment.
高血糖是已获批用于治疗某些晚期或转移性乳腺癌的磷脂酰肌醇3激酶(PI3K)抑制剂最常见的副作用。这种副作用可能是由于PI3K在胰岛素信号传导中的核心作用。在此,我们报告使用钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂来控制严重高血糖。
我们描述了一名74岁女性,在开始使用阿哌利西布(一种用于转移性乳腺癌的新型口服PI3K抑制剂)后出现严重的、难以控制的高血糖,尽管服用了口服降糖药二甲双胍和维格列汀,并联合每日高达250单位的静脉胰岛素输注。引入SGLT2抑制剂达格列净后,血糖迅速改善,胰岛素剂量从250单位/天大幅降至12单位/天,且无明显副作用。
我们报告了使用SGLT2抑制剂成功控制阿哌利西布诱导的高血糖,且无需中断有效的癌症治疗。