Repository logo
 
Publication

Hepatic immune-mediatedadverseeffects of immune checkpoint inhibitors: analysis of real-life experience

dc.contributor.authorSilva, Joana
dc.contributor.authorFalcão, Daniela
dc.contributor.authorCardoso, Cláudia
dc.contributor.authorPires, Ana Luísa
dc.contributor.authorAraújo, António
dc.contributor.authorCastro-Poças, Fernando
dc.date.accessioned2023-12-21T11:19:24Z
dc.date.available2023-12-21T11:19:24Z
dc.date.issued2021-12
dc.description.abstractIntroduction and objectives: Immune Checkpoint Inhibitors (ICI) have shifted the paradigm of cancer therapy treatment. Despite their efficacy, ICIs may induce immune-related adverse events (irAE), which can affect various organs, namely the liver. This study intends to perform a comprehensive clinical description of the hepatic irAEs associated with ICI in a Portuguese population of a tertiary hospital centre. Materials and methods: A retrospective analysis of patients who developed immune-mediated liver injury (IMLI), among a cohort of patients treated with ICIs between March 15th of 2015 and December 15th of 2019 in a tertiary hospital. We used both Common Terminology Criteria for Adverse Events (CTCAE) and Drug-Induced Liver Injury Network (DILIN) criteria to define liver injury. Results: Among 151 patients, eight (5.3%) patients developed liver injury grade ≥3, of which five had hepatic metastasis. As such, only 3 cases were classified as IMLI. All IMLI presented with cholestasis pattern; the median duration from ICI initiation to IMLI was 84 days and/or 4 ICI cycles; one patient registered IMLI one month after nivolumab suspension; all were treated with steroids and one was successfully submitted to ICI re-challenge; a favourable outcome was seen in all patients; the median time to hepatic biochemistries normalization was 150 days. Among 10 patients with previous hepatic conditions, only one developed liver injury grade 2. Conclusions: Clinically significant ICI-related hepatotoxicity was uncommon; Immune-mediated liver injury may present a cholestatic pattern predominance. There was a low rate of liver injury of any kind in patients with previous hepatic disease while on ICI.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationda Silva JA, Falcão D, Cardoso C, Pires AL, Araújo A, Castro-Poças F. Hepatic immune-mediatedadverseeffects of immune checkpoint inhibitors: analysis of real-life experience. Ann Hepatol. 2021;26:100561. doi:10.1016/j.aohep.2021.100561pt_PT
dc.identifier.doi10.1016/j.aohep.2021.100561pt_PT
dc.identifier.issn1665-2681
dc.identifier.urihttp://hdl.handle.net/10400.16/2897
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S166526812100260X?via%3Dihubpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectDrug Induced Liver Injurypt_PT
dc.subjectDrug-Related Side Effects and Adverse Reactionspt_PT
dc.subjectHepatotoxicitypt_PT
dc.subjectImmune-related adverse eventpt_PT
dc.subjectImmunotherapypt_PT
dc.subjectcancerpt_PT
dc.titleHepatic immune-mediatedadverseeffects of immune checkpoint inhibitors: analysis of real-life experiencept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceMexicopt_PT
oaire.citation.startPage100561pt_PT
oaire.citation.titleAnnals of Hepatologypt_PT
oaire.citation.volume26pt_PT
person.familyNameSilva
person.givenNameJoana
person.identifier.orcid0000-0003-4065-2102
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication08d33369-30b0-426e-a79c-532239f174e9
relation.isAuthorOfPublication.latestForDiscovery08d33369-30b0-426e-a79c-532239f174e9

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Silva_2021_hepatic.pdf
Size:
506.62 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.44 KB
Format:
Item-specific license agreed upon to submission
Description: