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dc.contributor.authorMulla, K
dc.contributor.authorFarag, S
dc.contributor.authorMoore, B
dc.contributor.authorMatharu, S
dc.contributor.authorYoung, K
dc.contributor.authorLarkin, J
dc.contributor.authorPopat, S
dc.contributor.authorMorganstein, DL
dc.coverage.spatialEngland
dc.date.accessioned2023-05-02T09:29:28Z
dc.date.available2023-05-02T09:29:28Z
dc.date.issued2023-04-01
dc.identifier.citationDiabetic Medicine, 2023, 40 (4), pp. e15053 -en_US
dc.identifier.issn0742-3071
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5772
dc.identifier.eissn1464-5491
dc.identifier.eissn1464-5491
dc.identifier.doi10.1111/dme.15053
dc.description.abstractAIMS: We systematically studied the presence of hyperglycaemia during treatment with Immune Checkpoint Inhibitors (ICPI) for cancer, in those with and without diabetes at baseline, and determined the cause of new-onset hyperglycaemia, METHODS: Retrospective review of electronic records of those receiving an ICPI for melanoma, lung or renal cancer. RESULTS: Overall, 959 participants were included. In this study, 103 had diabetes at baseline (10.7%). Those with lung cancer had the highest frequency of diabetes; 131 people had hyperglycaemia (defined as at least one glucose ≥11.1 mmol/L) in the year after starting an ICPI. The incidence was 55% in those with diabetes at baseline, and 8.6% in those without baseline diabetes. Among 74 with new-onset hyperglycaemia (without pre-existing diabetes) 76% was attributable to steroid induced diabetes, with 9.5% due to ICPI Induced diabetes resembling type 1 diabetes. CONCLUSIONS: Hyperglycaemia is common in persons receiving an ICPI for cancer, including 8.6% of those without known diabetes. While much of this is due to glucocorticoid use, care is needed to avoid missing those with ICPI-induced diabetes who are at risk of diabetic ketoacidosis, which is a medical emergency.
dc.formatPrint-Electronic
dc.format.extente15053 -
dc.languageeng
dc.language.isoengen_US
dc.publisherWILEYen_US
dc.relation.ispartofDiabetic Medicine
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0en_US
dc.subjectcancer
dc.subjectclinical diabetes
dc.subjectHumans
dc.subjectHyperglycemia
dc.subjectImmune Checkpoint Inhibitors
dc.subjectIncidence
dc.subjectDiabetes Mellitus, Type 1
dc.subjectLung Neoplasms
dc.titleHyperglycaemia following immune checkpoint inhibitor therapy-Incidence, aetiology and assessment.en_US
dc.typeJournal Article
dcterms.dateAccepted2023-01-23
dc.date.updated2023-05-02T09:28:58Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1111/dme.15053en_US
rioxxterms.licenseref.startdate2023-04-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36696014
pubs.issue4
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1111/dme.15053
pubs.volume40
dc.contributor.icrauthorPopat, Sanjay
icr.provenanceDeposited by Mr Arek Surman (impersonating Prof Robert Huddart) on 2023-05-02. Deposit type is initial. No. of files: 1. Files: Diabetic Medicine - 2023 - Mulla - Hyperglycaemia following immune checkpoint inhibitor therapy Incidence aetiology and.pdf


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