# Diabetic Ketoacidosis With the Use of Alpelisib in a Patient With Metastatic Breast Cancer Without Diabetes

**Authors:** Lakshmi Polisetty, Sneha Teresa Selvin, Jia Wei Tan

PMC · DOI: 10.1210/jcemcr/luae023 · 2024-03-22

## TL;DR

A patient with metastatic breast cancer developed diabetic ketoacidosis (DKA) from alpelisib, a drug used to treat certain breast cancers, despite having no prior diabetes.

## Contribution

This case report highlights alpelisib-induced DKA in a non-diabetic patient and suggests management strategies.

## Key findings

- Alpelisib can cause DKA in non-diabetic patients with metastatic breast cancer.
- Hyperglycemia occurred rapidly after alpelisib initiation and led to permanent drug discontinuation.
- Intravenous insulin and hydration resolved DKA, and sitagliptin was used for post-discharge management.

## Abstract

Diabetic ketoacidosis (DKA) is a life-threatening medical condition. Alpelisib, a new drug used to treat phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha mutated breast cancer, is reported to cause DKA as a rare adverse effect. We present a case of alpelisib-induced DKA in a patient with metastatic breast cancer without diabetes. An 81-year-old female with a history of hormone receptor-positive, human epidermal growth factor receptor 2-negative metastatic breast cancer presented to the emergency room with clinical features and blood work consistent with DKA. She was started on alpelisib 6 weeks before her presentation to the hospital. She did not have a documented history of diabetes. Upon admission, alpelisib was held, and her blood glucose returned to baseline with intravenous insulin and hydration. Post-discharge, she was managed with sitagliptin. Subsequent attempts to reintroduce alpelisib were associated with hyperglycemia, which led to the permanent discontinuation of alpelisib and the transition to alternative treatment options. Alpelisib causes hyperglycemia by inhibiting the phosphatidylinositol 3-kinase/activated protein kinase-B pathway, which regulates blood glucose levels. This case report illustrates DKA as a presenting symptom and provides potential management options for alpelisib-induced DKA. Hyperglycemia is a frequent adverse effect of alpelisib in patients with diabetes. This case report is unique as our patient developed uncontrolled diabetes within a few weeks after initiation of alpelisib.

## Linked entities

- **Chemicals:** alpelisib (PubChem CID 56649450), sitagliptin (PubChem CID 4369359), insulin (PubChem CID 70678557)
- **Diseases:** diabetic ketoacidosis (MONDO:0012819)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** DKA (MESH:D016883), Breast Cancer (MESH:D001943), Diabetes (MESH:D003920), Metastatic (MESH:D000092182), Hyperglycemia (MESH:D006943)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10959061/full.md

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Source: https://tomesphere.com/paper/PMC10959061