Spanjaard Pamela, Petit Jean Michel, Schmitt Antonin, Vergès Bruno, Bouillet Benjamin
Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, Dijon, France.
Department of Endocrinology, Diabetes and Metabolic Disorders, Dijon University Hospital, Dijon, France; Inserm Unit, LNC-UMR 1231, University of Burgundy, Dijon, France.
Ann Endocrinol (Paris). 2024 Jul;85(4):263-268. doi: 10.1016/j.ando.2023.11.003. Epub 2023 Dec 1.
Inhibitors of mTOR (mTORi) are frequently used as anticancer treatment. They were responsible for metabolic side-effects in phase 3 studies, which provided only an incomplete picture of these metabolic complications. The aim of our study was therefore to evaluate, in a real-life setting, outcomes for patients with dyslipidemia or diabetes under mTORi, and the incidence and management of metabolic abnormalities occurring under mTORi in the absence of known metabolic history.
This single-center retrospective study included all 177 patients receiving everolimus in the Cancer Center of Dijon, France, between May 2015 and November 2018.
Diabetes was diagnosed in 15 patients (9%), with an estimated mean time to onset of 160±173 days. Antidiabetic treatment was introduced in 41% of these patients. After mTORi discontinuation, diabetes persisted in 60% of patients in whom it had been diagnosed. Dyslipidemia was diagnosed in 22 patients (14%): 55% with hypercholesterolemia and 45% with hypertriglyceridemia. 18% were placed on lipid-lowering therapy. While all patients were screened for hyperglycemia and monitored for known diabetes, only 42% of patients without dyslipidemia were screened for lipids, and only 8% of patients with known dyslipidemia were monitored for lipids.
Our study is one of the few to look at metabolic complications secondary to mTORi in a real-life situation. The incidence of diabetes was high, but the use of antidiabetic treatment was variable. Normalization of glucose homeostasis after mTORi discontinuation is possible, particularly in patients who have not been placed on antidiabetic therapy. Screening for dyslipidemia was clearly inadequate in our study, making the data on this point more difficult to interpret. It appears that adherence to guidelines needs to be improved to optimize the management of patients treated with mTORi.
mTOR抑制剂(mTORi)常被用作抗癌治疗药物。在3期研究中,它们会引发代谢副作用,但这些研究对这些代谢并发症的描述并不完整。因此,我们研究的目的是在实际临床环境中评估接受mTORi治疗的血脂异常或糖尿病患者的治疗结果,以及在无已知代谢病史的情况下接受mTORi治疗时发生的代谢异常的发生率和管理情况。
这项单中心回顾性研究纳入了2015年5月至2018年11月期间在法国第戎癌症中心接受依维莫司治疗的所有177例患者。
15例患者(9%)被诊断为糖尿病,估计平均发病时间为160±173天。其中41%的患者开始接受抗糖尿病治疗。在停用mTORi后,60%已被诊断为糖尿病的患者糖尿病仍持续存在。22例患者(14%)被诊断为血脂异常:55%为高胆固醇血症,45%为高甘油三酯血症。18%的患者接受了降脂治疗。虽然所有患者都接受了高血糖筛查并对已知糖尿病患者进行了监测,但只有42%的无血脂异常患者接受了血脂筛查,只有8%的已知血脂异常患者接受了血脂监测。
我们的研究是少数几项在实际临床环境中观察mTORi继发代谢并发症的研究之一。糖尿病的发生率较高,但抗糖尿病治疗的使用情况不一。停用mTORi后血糖稳态有可能恢复正常,尤其是那些未接受抗糖尿病治疗的患者。在我们的研究中,血脂异常筛查明显不足,使得这方面的数据更难解读。似乎需要加强对指南的遵循,以优化接受mTORi治疗患者的管理。