[Toxic manifestations of alpelisib in endocrinology. Description of the clinical case].

L M Kudaeva, E E Kozhedub, V O Kupryshina, T Z Aliyev, E A Troshina
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Abstract

Breast cancer (BC) is a serious disease and is considered an important health problem worldwide. The prevalence of the disease in women according to Rosstat was 64,951 cases in the Russian Federation in 2020 (21.7% among all types of cancer).  Hormone-dependent estrogen receptor-positive (HR+), human epidermal growth factor receptor type 2 negative (HER2-) metastatic breast cancer (mBC) accounts for 70% of all cases.  About 40% of patients with ER+/HER2- mBC have mutations in the PIK3CA gene, leading to hyperactivation of the alpha isoform (p110α) of phosphatidylinositol 3-kinase (PI3K). Hormonal therapy with or without cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor is considered the standard treatment for patients with ER+/HER2- mBC. However, acquired resistance to this therapy remains a problem. Innovative methods for the treatment of breast cancer are the use of targeted therapeutic agents aimed at direct inhibition of the PI3K pathway in combination with hormone therapy. Alpelisib is a PI3Kα-specific inhibitor. Hyperglycemia is the most common side effect of alpelisib treatment. Currently, there is a consensus on the prevention and correction of hyperglycemia in patients receiving therapy with alpelisib, which recommends that before starting therapy, in  order to diagnose carbohydrate metabolism disorders and assess the risk of developing hyperglycemia, determine in all patients: the level of glycated hemoglobin (HbA1c), glucose fasting plasma (FPG), body mass index (BMI). And also to evaluate such risk factors as the presence of a family history of type 2 diabetes mellitus (DM 2), the presence of gestational diabetes in the patient's history, or the fact of the birth of children weighing more than 4 kilograms.Recently, new combinations of drugs have been actively used to treat disorders of carbohydrate metabolism, such as pioglitazone + metformin. This paper discusses the mechanism of action of PI3K inhibitors, new therapeutic combinations and their undesirable effects, and presents therapeutic experience.

[阿来替尼在内分泌学中的毒性表现。临床病例描述]。
乳腺癌(BC)是一种严重的疾病,在全世界都被认为是一个重要的健康问题。根据俄罗斯统计局的数据,2020 年俄罗斯联邦妇女的乳腺癌发病率为 64 951 例(在所有癌症类型中占 21.7%)。 激素依赖性雌激素受体阳性(HR+)、人表皮生长因子受体 2 型阴性(HER2-)的转移性乳腺癌(mBC)占所有病例的 70%。 约 40% 的 ER+/HER2- mBC 患者的 PIK3CA 基因发生突变,导致磷脂酰肌醇 3- 激酶(PI3K)α 异构体(p110α)过度激活。激素治疗联合或不联合细胞周期蛋白依赖性激酶4和6(CDK4/6)抑制剂被认为是治疗ER+/HER2- mBC患者的标准疗法。然而,这种疗法的获得性耐药性仍然是一个问题。治疗乳腺癌的创新方法是将旨在直接抑制 PI3K 通路的靶向治疗药物与激素疗法相结合。Alpelisib是一种PI3Kα特异性抑制剂。高血糖是 Alpelisib 治疗最常见的副作用。目前,关于预防和纠正接受阿来替尼治疗的患者的高血糖已达成共识,建议在开始治疗前,为了诊断碳水化合物代谢紊乱和评估发生高血糖的风险,应确定所有患者的糖化血红蛋白(HbA1c)水平、空腹血浆葡萄糖(FPG)、体重指数(BMI)。此外,还要评估风险因素,如是否有 2 型糖尿病(DM 2)家族史、患者是否有妊娠糖尿病史、是否生育过体重超过 4 公斤的孩子等。最近,人们积极使用新的药物组合来治疗碳水化合物代谢紊乱,如吡格列酮+二甲双胍。本文讨论了 PI3K 抑制剂的作用机制、新的治疗组合及其不良反应,并介绍了治疗经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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