C-Peptide and BMi predict anti-hyperglycemic treatment lines in breast cancer patients treated with Alpelisib.

IF 3.7 3区 医学 Q2 Medicine
Endocrine Pub Date : 2024-11-01 Epub Date: 2024-07-04 DOI:10.1007/s12020-024-03924-y
Elena Carrillo-Lopez, Fernando Sebastian-Valles, Carolina Sager La Ganga, Anabel Ballesteros, Victor Navas-Moreno, Dulce Bañón, María Pilar López Martí, Mónica Marazuela, José Alfonso Arranz Martín
{"title":"C-Peptide and BMi predict anti-hyperglycemic treatment lines in breast cancer patients treated with Alpelisib.","authors":"Elena Carrillo-Lopez, Fernando Sebastian-Valles, Carolina Sager La Ganga, Anabel Ballesteros, Victor Navas-Moreno, Dulce Bañón, María Pilar López Martí, Mónica Marazuela, José Alfonso Arranz Martín","doi":"10.1007/s12020-024-03924-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Alpelisib is a PI3K (Phosphoinositide 3-kinases) inhibitor used for breast cancer which develops hyperglycemia based on its action on glucose metabolism regulation. This study aims to identify potential risk factors predicting hyperglycemia development and the need for multiple treatments for hyperglycemia in patients receiving Alpelisib.</p><p><strong>Methods: </strong>Fourteen women diagnosed with metastatic hormone receptor-positive breast cancer carrying PI3K mutations who initiated treatment with Alpelisib were monitored through consultations in the Oncology and Endocrinology departments. Non-parametric ROC curves were generated to assess the need for three or more antidiabetic medications to achieve glycemic control.</p><p><strong>Results: </strong>The study population had a median age of 64 years (range:48-69) with a median body mass index (BMI) of 26.6 kg/m<sup>2</sup> (range: 22.9-29.4). Overweight was observed in 35.7% of the participants and obesity in 21.4%. Fifty percent of the participants had prediabetes, and 85.7% developed hyperglycemia requiring pharmacological treatment, although none of them needed to discontinue treatment for this reason. Baseline C-peptide levels and BMI were associated with the number of antidiabetic drugs used (Spearman's Rho 0.553, p = 0.040; Spearman's Rho 0.581, p = 0.030, respectively). ROC curve analysis showed and area under the curve (AUC) of 0.819 for the variable risk profile (defined as baseline C-peptide >10.5 ng/ml and BMI > 27 kg/m<sup>2</sup>), whereas AUC values were 0.556 and 0.514 for HbA1c and baseline glucose, respectively, (p = 0.012).</p><p><strong>Conclusion: </strong>A joint follow-up by an Oncology department and a Diabetes Unit can prevent treatment discontinuation in patients under Alpelisib therapy. Baseline BMI and plasma C-peptide levels can predict an increased need for anti-hyperglycemic treatment.</p>","PeriodicalId":11572,"journal":{"name":"Endocrine","volume":" ","pages":"470-477"},"PeriodicalIF":3.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11489167/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12020-024-03924-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/4 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: Alpelisib is a PI3K (Phosphoinositide 3-kinases) inhibitor used for breast cancer which develops hyperglycemia based on its action on glucose metabolism regulation. This study aims to identify potential risk factors predicting hyperglycemia development and the need for multiple treatments for hyperglycemia in patients receiving Alpelisib.

Methods: Fourteen women diagnosed with metastatic hormone receptor-positive breast cancer carrying PI3K mutations who initiated treatment with Alpelisib were monitored through consultations in the Oncology and Endocrinology departments. Non-parametric ROC curves were generated to assess the need for three or more antidiabetic medications to achieve glycemic control.

Results: The study population had a median age of 64 years (range:48-69) with a median body mass index (BMI) of 26.6 kg/m2 (range: 22.9-29.4). Overweight was observed in 35.7% of the participants and obesity in 21.4%. Fifty percent of the participants had prediabetes, and 85.7% developed hyperglycemia requiring pharmacological treatment, although none of them needed to discontinue treatment for this reason. Baseline C-peptide levels and BMI were associated with the number of antidiabetic drugs used (Spearman's Rho 0.553, p = 0.040; Spearman's Rho 0.581, p = 0.030, respectively). ROC curve analysis showed and area under the curve (AUC) of 0.819 for the variable risk profile (defined as baseline C-peptide >10.5 ng/ml and BMI > 27 kg/m2), whereas AUC values were 0.556 and 0.514 for HbA1c and baseline glucose, respectively, (p = 0.012).

Conclusion: A joint follow-up by an Oncology department and a Diabetes Unit can prevent treatment discontinuation in patients under Alpelisib therapy. Baseline BMI and plasma C-peptide levels can predict an increased need for anti-hyperglycemic treatment.

Abstract Image

C肽和BMi可预测接受Alpelisib治疗的乳腺癌患者的抗高血糖治疗方案。
目的:Alpelisib是一种用于治疗乳腺癌的PI3K(磷脂酰肌醇3-激酶)抑制剂,由于其对葡萄糖代谢的调节作用,会导致高血糖。本研究旨在确定预测高血糖发生的潜在风险因素,以及接受 Alpelisib 治疗的患者是否需要对高血糖进行多种治疗:方法:通过肿瘤科和内分泌科的会诊,对14名确诊为携带PI3K突变的转移性激素受体阳性乳腺癌并开始接受Alpelisib治疗的女性患者进行监测。研究人员绘制了非参数 ROC 曲线,以评估是否需要使用三种或三种以上的抗糖尿病药物才能达到血糖控制:研究对象的中位年龄为 64 岁(范围:48-69),中位体重指数(BMI)为 26.6 kg/m2(范围:22.9-29.4)。35.7%的参与者超重,21.4%的参与者肥胖。50%的参与者患有糖尿病前期,85.7%的参与者出现了需要药物治疗的高血糖,但没有人因此而停止治疗。基线 C 肽水平和体重指数与使用的抗糖尿病药物数量相关(分别为 Spearman's Rho 0.553,p = 0.040;Spearman's Rho 0.581,p = 0.030)。ROC曲线分析显示,可变风险曲线(定义为基线C肽>10.5纳克/毫升和体重指数>27千克/平方米)的曲线下面积(AUC)为0.819,而HbA1c和基线血糖的AUC值分别为0.556和0.514(p = 0.012):结论:肿瘤科和糖尿病科联合随访可防止接受阿来替尼治疗的患者中断治疗。基线体重指数和血浆C肽水平可预测抗高血糖治疗需求的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Endocrine
Endocrine 医学-内分泌学与代谢
CiteScore
6.40
自引率
5.40%
发文量
0
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信