Leung Mova, Rodrigues Paulina, Roitman Daryl
Cancer Care Program, North York General Hospital, Toronto, Ontario, Canada.
Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.
Onco Targets Ther. 2022 Oct 28;15:1309-1315. doi: 10.2147/OTT.S370244. eCollection 2022.
Diabetic ketoacidosis (DKA) is a rare complication of alpelisib, but cases of DKA are reported. Alpelisib's safety in patients with long-standing, suboptimally controlled diabetes is unclear since clinical trials of alpelisib did not include them.
A case is presented on a patient with metastatic breast cancer and type 2 diabetes admitted for DKA eleven days after starting alpelisib. Since DKA is implicated in antihyperglycemics that inhibit sodium-glucose cotransporter-2 (SGLT2) inhibitors, her empagliflozin was discontinued. Alpelisib was also held since it was recently initiated. After the DKA resolved, she was discharged and restarted alpelisib. Within 4 hours of taking the first dose, the patient developed a second episode of DKA, and alpelisib treatment was stopped permanently.
Patients with long-standing type 2 diabetes are at high risk of alpelisib-induced Grade 3 and 4 hyperglycemia, including DKA. It is essential to communicate with non-oncology stakeholders about the risk of DKA with alpelisib as it can be overlooked for more common causes. Restarting alpelisib can result in severe hyperglycemia or DKA within 24 hours of the first dose. In this population, the risks associated with rechallenging alpelisib must be heavily weighed against its benefits. Before restarting alpelisib, a thorough evaluation of the appropriateness of the patient's antihyperglycemics and diet must occur to anticipate and mitigate a second event. Antihyperglycemics independent of the PI3K/AKT/mTOR pathway may be preferred agents. A plan should be in place to quickly respond to rising glycemia and early referral to a diabetologist or endocrinologist is recommended. Continuous glucose monitoring and hospital admission are recommended during rechallenge. A better understanding of alpelisib-induced hyperglycemia, especially in patients with diabetes, is required to navigate alpelisib treatment safely. Emphasis should be placed on patient education of symptoms and monitoring parameters.
糖尿病酮症酸中毒(DKA)是阿哌利西布罕见的并发症,但有DKA病例的报道。由于阿哌利西布的临床试验未纳入长期血糖控制不佳的糖尿病患者,其在这类患者中的安全性尚不清楚。
本文介绍了一名转移性乳腺癌合并2型糖尿病患者,在开始使用阿哌利西布11天后因DKA入院。由于DKA与抑制钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂的降糖药有关,她停用了恩格列净。阿哌利西布也因最近开始使用而停用。DKA缓解后,她出院并重新开始使用阿哌利西布。在服用首剂后的4小时内,患者出现了第二次DKA发作,阿哌利西布治疗被永久停止。
长期2型糖尿病患者发生阿哌利西布诱发的3级和4级高血糖(包括DKA)的风险很高。必须与非肿瘤学利益相关者沟通阿哌利西布导致DKA的风险,因为它可能因更常见的原因而被忽视。重新开始使用阿哌利西布可能会在首剂后的24小时内导致严重高血糖或DKA。在这一人群中,重新使用阿哌利西布的风险必须与其益处进行权衡。在重新开始使用阿哌利西布之前,必须对患者降糖药和饮食的适宜性进行全面评估,以预测和减轻再次发作。独立于PI3K/AKT/mTOR途径的降糖药可能是首选药物。应制定应对血糖升高的快速反应计划,建议尽早转诊给糖尿病专家或内分泌专家。重新用药期间建议进行持续血糖监测并住院。为了安全地进行阿哌利西布治疗,需要更好地了解阿哌利西布诱发的高血糖,尤其是糖尿病患者。应重点对患者进行症状和监测参数的教育。