Alpelisib-Induced Diabetic Ketoacidosis.

adverse drug events alpelisib breast cancer diabetic ketoacidosis hyperglycemia intensive care oncology piqray

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
01 May 2021
Historique:
entrez: 4 6 2021
pubmed: 5 6 2021
medline: 5 6 2021
Statut: epublish

Résumé

We present the third case of alpelisib-induced diabetic ketoacidosis. Alpelisib is an antineoplastic agent that inhibits phosphatidylinositol 3-kinase (PI3K), which plays a key role in multiple biological processes such as cell differentiation, proliferation, and survival. Thereby, the inhibition of this pathway should cause antitumor activity. Alpelisib was recently approved by the Food and Drug Administration (FDA) for use in PIK3CA-mutated breast cancer. This mutation is a common indicator of poor prognosis and is also the most commonly mutated gene in hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer. During its trial, ketoacidosis was reported in only 0.7% of patients, with the more common side effects (>20%) being diarrhea (58%), rash (52%), nausea (45%), fatigue (42%), decreased appetite (36%), stomatitis (30%), vomiting (27%), weight loss (27%), and alopecia (20%). As breast cancer is the second most common cancer in women and approximately 40% of HR+/HER2- advanced breast cancer patients have a PIK3CA mutation, alpelisib will be prescribed more by oncologists and, therefore, appropriate screening with fasting plasma glucose, hemoglobin A1c (HbA1C), and monitoring during drug administration is of utmost importance.

Identifiants

pubmed: 34084688
doi: 10.7759/cureus.14796
pmc: PMC8166359
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e14796

Informations de copyright

Copyright © 2021, Nguyen et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Nature. 2018 Aug;560(7719):499-503
pubmed: 30051890
J Clin Invest. 2004 Oct;114(7):928-36
pubmed: 15467831
N Engl J Med. 2019 May 16;380(20):1929-1940
pubmed: 31091374
MMWR Morb Mortal Wkly Rep. 2018 Mar 30;67(12):362-365
pubmed: 29596400
Int J Biol Sci. 2018 Aug 6;14(11):1483-1496
pubmed: 30263000
Cancer. 2019 Apr 1;125(7):1185-1199
pubmed: 30582752
Cell. 2017 Apr 20;169(3):381-405
pubmed: 28431241
Cell Metab. 2007 Apr;5(4):237-52
pubmed: 17403369

Auteurs

Paul Nguyen (P)

Internal Medicine, Wayne State University School of Medicine, Detroit, USA.

Aya Musa (A)

Endocrinology, Diabetes and Metabolism, Wayne State University School of Medicine, Detroit, USA.

Julie Samantray (J)

Endocrine Oncology, Karmanos Cancer Center, Detroit, USA.
Endocrinology, Diabetes and Metabolism, Wayne State University School of Medicine, Detroit, USA.

Classifications MeSH