Ceritinib Aggravates Glycemic Control in Insulin-treated Patients with Diabetes and Metastatic ALK-positive Lung Cancer.


Journal

Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241

Informations de publication

Date de publication:
15 Mar 2019
Historique:
pubmed: 20 11 2018
medline: 6 5 2019
entrez: 20 11 2018
Statut: ppublish

Résumé

We herein report a 75-year-old woman with insulin-treated diabetes and metastatic anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer who received ceritinib, a second-generation ALK inhibitor, and achieved dramatic tumor reduction. However, her fasting blood glucose increased, particularly markedly in the first two weeks after ceritinib administration, and did not normalize even increasing the total insulin dose. After discontinuing ceritinib, her glucose levels rapidly reduced. Ceritinib can aggravate hyperglycemia in patients with diabetes who lack compensatory insulin secretion, due to its inhibitory effects on the insulin receptor. Careful monitoring for ceritinib-induced hyperglycemia should be performed, especially in the first two weeks after ceritinib administration.

Identifiants

pubmed: 30449809
doi: 10.2169/internalmedicine.1870-18
pmc: PMC6465015
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers 0
Biomarkers, Tumor 0
Blood Glucose 0
Hypoglycemic Agents 0
Insulins 0
Pyrimidines 0
Sulfones 0
ALK protein, human EC 2.7.10.1
Anaplastic Lymphoma Kinase EC 2.7.10.1
ceritinib K418KG2GET

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

817-820

Références

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pubmed: 17625570
N Engl J Med. 2014 Mar 27;370(13):1189-97
pubmed: 24670165
Clin Cancer Res. 2015 Jun 1;21(11):2436-9
pubmed: 25754348
Cancer Discov. 2016 Oct;6(10):1118-1133
pubmed: 27432227
J Clin Oncol. 2016 Aug 20;34(24):2866-73
pubmed: 27432917
Pharmacol Res. 2017 Mar;117:343-356
pubmed: 28077299
Lancet. 2017 Mar 4;389(10072):917-929
pubmed: 28126333
Cancer Treat Rev. 2017 Apr;55:181-189
pubmed: 28427013

Auteurs

Ikki Sakuma (I)

Department of Clinical Cell Biology & Medicine, Chiba University Graduate School of Medicine, Japan.
Division of Endocrinology & Metabolism, Chiba University Hospital, Japan.

Hidekazu Nagano (H)

Department of Clinical Cell Biology & Medicine, Chiba University Graduate School of Medicine, Japan.
Division of Endocrinology & Metabolism, Chiba University Hospital, Japan.

Ichiro Yoshino (I)

Department of General Thoracic Surgery, Chiba University Graduate School of Medicine, Japan.

Koutaro Yokote (K)

Department of Clinical Cell Biology & Medicine, Chiba University Graduate School of Medicine, Japan.
Division of Endocrinology & Metabolism, Chiba University Hospital, Japan.

Tomoaki Tanaka (T)

Division of Endocrinology & Metabolism, Chiba University Hospital, Japan.
Department of Molecular Diagnosis, Chiba University Graduate School of Medicine, Japan.

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Classifications MeSH