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dc.contributor.authorAndres, MS
dc.contributor.authorRamalingam, S
dc.contributor.authorRosen, SD
dc.contributor.authorBaksi, J
dc.contributor.authorKhattar, R
dc.contributor.authorKirichenko, Y
dc.contributor.authorYoung, K
dc.contributor.authorYousaf, N
dc.contributor.authorOkines, A
dc.contributor.authorHuddart, R
dc.contributor.authorHarrington, K
dc.contributor.authorFurness, AJS
dc.contributor.authorTurajlic, S
dc.contributor.authorPickering, L
dc.contributor.authorPopat, S
dc.contributor.authorLarkin, J
dc.contributor.authorLyon, AR
dc.coverage.spatialEngland
dc.date.accessioned2023-02-21T13:37:01Z
dc.date.available2023-02-21T13:37:01Z
dc.date.issued2022-11-24
dc.identifierARTN 21
dc.identifier10.1186/s40959-022-00147-w
dc.identifier.citationCardio-Oncology, 2022, 8 (1), pp. 21 -
dc.identifier.issn2057-3804
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5697
dc.identifier.eissn2057-3804
dc.identifier.eissn2057-3804
dc.identifier.doi10.1186/s40959-022-00147-w
dc.description.abstractBACKGROUND: The full range of cardiovascular complications related to the use of Immune checkpoint inhibitors (ICI) is not fully understood. We aim to describe the spectrum of cardiovascular adverse events (cvAEs) by presenting our real-world experience of the diagnosis and management of these complications. METHODS: Two thousand six hundred and forty-seven (2647) patients were started on ICI treatment between 2014 and 2020. Data from 110 patients referred to the cardio-oncology service with a suspected cvAE was collected prospectively and analysed. RESULTS: Eighty-nine patients (3.4%) were confirmed to have cvAEs while on ICI therapy. Myocarditis was the most frequent event (33/89), followed by tachyarrhythmia (27/89), non-inflammatory left ventricular dysfunction (NILVD) (15/89) and pericarditis (7/89). Results from myocarditis and non-inflammatory left ventricular dysfunction cohorts were compared. Myocarditis and NILVD showed significant differences in respect toof troponin elevation, cardiac magnetic resonance abnormalities and ventricular function. Dual ICI therapy and other immune related adverse events were more frequently associated with myocarditis than NILVD. There was a significant difference in the median time from starting ICI treatment to presentation with myocarditis versus NILVD (12 vs 26 weeks p = 0.049). Through early recognition of myocarditis, prompt treatment with steroids and interruption of ICI, there were no cardiovascular in-hospital deaths. NILVD did not require steroid treatment and ICI could be restarted safely. CONCLUSIONS: The full spectrum of cardiovascular complications in patients with immune checkpoint inhibitors is much broader than initially described. Myocarditis remains the most frequent cvAE related to ICI treatment. A novel type of myocardial injury was observed and defined as Atrial tachyarrhythmias and NILVD were also frequent in this cohort. NILVD has a This differs fromdifferent presentation from ICI-related myocarditis, mainly usually presenting afterby the lack of inflammatory features on CMR and biomarkers and a later presentation in time.
dc.formatElectronic
dc.format.extent21 -
dc.languageeng
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofCardio-Oncology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCancer survivorship
dc.subjectCardiomyopathy
dc.subjectImmunotherapy
dc.subjectMyocarditis
dc.titleThe spectrum of cardiovascular complications related to immune-checkpoint inhibitor treatment : Including myocarditis and the new entity of non inflammatory left ventricular dysfunction.
dc.typeJournal Article
dcterms.dateAccepted2022-11-07
dc.date.updated2023-02-21T13:36:10Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1186/s40959-022-00147-w
rioxxterms.licenseref.startdate2022-11-24
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36424659
pubs.issue1
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/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Melanoma and Kidney Cancer
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Melanoma and Kidney Cancer/Melanoma and Kidney Cancer (hon.)
pubs.organisational-group/ICR/ImmNet
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1186/s40959-022-00147-w
pubs.volume8
icr.researchteamClinic Acad RT Huddart
icr.researchteamTargeted Therapy
icr.researchteamSkin Unit
dc.contributor.icrauthorHuddart, Robert
dc.contributor.icrauthorHarrington, Kevin
dc.contributor.icrauthorFurness, Andrew
icr.provenanceDeposited by Mr Arek Surman on 2023-02-21. Deposit type is initial. No. of files: 1. Files: The spectrum of cardiovascular complications related to immune-checkpoint inhibitor treatment Including myocarditis and the.pdf


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