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SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report
BACKGROUND: Hyperglycemia is the most common side-effect of phosphatidylinositol 3-kinase (PI3K) inhibitors that are approved for the treatment of some advanced or metastatic breast cancers. This side-effect is likely due to the central role of PI3K in insulin signalling. Here we report the use of a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290528/ https://www.ncbi.nlm.nih.gov/pubmed/34281618 http://dx.doi.org/10.1186/s40842-021-00125-8 |
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author | Sahakian, Nicolas Cattieuw, Lauranne Ramillon-Cury, Clotilde Corroller, Audrey Bégu-Le Silvestre-Aillaud, Pascale Béliard, Sophie Valéro, René |
author_facet | Sahakian, Nicolas Cattieuw, Lauranne Ramillon-Cury, Clotilde Corroller, Audrey Bégu-Le Silvestre-Aillaud, Pascale Béliard, Sophie Valéro, René |
author_sort | Sahakian, Nicolas |
collection | PubMed |
description | BACKGROUND: Hyperglycemia is the most common side-effect of phosphatidylinositol 3-kinase (PI3K) inhibitors that are approved for the treatment of some advanced or metastatic breast cancers. This side-effect is likely due to the central role of PI3K in insulin signalling. Here we report the use of a sodium-glucose cotransporter 2 (SGLT2) inhibitor to manage severe hyperglycemia. CASE PRESENTATION: We describe a 74-year-old woman who developed severe uncontrolled hyperglycemia after commencing alpelisib, a new oral PI3K inhibitor indicated for a metastatic breast cancer, despite taking oral anti-diabetic drugs, metformin and vildagliptin, combined with intravenous insulin infusion of up to 250 units/day. The introduction of the SGLT2 inhibitor dapagliflozin rapidly improved blood glucose with a drastic reduction in insulin dosage, from 250 to 12 units/day, and without significant side-effects. CONCLUSIONS: We report the successful management of hyperglycemia induced by alpelisib using a SGLT2 inhibitor without the need to discontinue effective cancer treatment. |
format | Online Article Text |
id | pubmed-8290528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82905282021-07-20 SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report Sahakian, Nicolas Cattieuw, Lauranne Ramillon-Cury, Clotilde Corroller, Audrey Bégu-Le Silvestre-Aillaud, Pascale Béliard, Sophie Valéro, René Clin Diabetes Endocrinol Case Report BACKGROUND: Hyperglycemia is the most common side-effect of phosphatidylinositol 3-kinase (PI3K) inhibitors that are approved for the treatment of some advanced or metastatic breast cancers. This side-effect is likely due to the central role of PI3K in insulin signalling. Here we report the use of a sodium-glucose cotransporter 2 (SGLT2) inhibitor to manage severe hyperglycemia. CASE PRESENTATION: We describe a 74-year-old woman who developed severe uncontrolled hyperglycemia after commencing alpelisib, a new oral PI3K inhibitor indicated for a metastatic breast cancer, despite taking oral anti-diabetic drugs, metformin and vildagliptin, combined with intravenous insulin infusion of up to 250 units/day. The introduction of the SGLT2 inhibitor dapagliflozin rapidly improved blood glucose with a drastic reduction in insulin dosage, from 250 to 12 units/day, and without significant side-effects. CONCLUSIONS: We report the successful management of hyperglycemia induced by alpelisib using a SGLT2 inhibitor without the need to discontinue effective cancer treatment. BioMed Central 2021-07-20 /pmc/articles/PMC8290528/ /pubmed/34281618 http://dx.doi.org/10.1186/s40842-021-00125-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Sahakian, Nicolas Cattieuw, Lauranne Ramillon-Cury, Clotilde Corroller, Audrey Bégu-Le Silvestre-Aillaud, Pascale Béliard, Sophie Valéro, René SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title | SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title_full | SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title_fullStr | SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title_full_unstemmed | SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title_short | SGLT2 inhibitors as potentially helpful drugs in PI3K inhibitor-induced diabetes: a case report |
title_sort | sglt2 inhibitors as potentially helpful drugs in pi3k inhibitor-induced diabetes: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290528/ https://www.ncbi.nlm.nih.gov/pubmed/34281618 http://dx.doi.org/10.1186/s40842-021-00125-8 |
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