Timeline of Adverse Events during Immune Checkpoint Inhibitors for Advanced Melanoma and Their Impacts on Survival

dc.contributor.authorVilla Crespo, Lorena
dc.contributor.authorPodlipnik, Sebastian
dc.contributor.authorAnglada, Natalia
dc.contributor.authorIzquierdo, Clara
dc.contributor.authorGiavedoni, Priscila
dc.contributor.authorIglesias, Pablo
dc.contributor.authorDominguez, Mireia
dc.contributor.authorAya, Francisco
dc.contributor.authorArance, Ana
dc.contributor.authorMalvehy, J. (Josep)
dc.contributor.authorPuig i Sardà, Susana
dc.contributor.authorCarrera Álvarez, Cristina
dc.date.accessioned2023-08-02T11:13:06Z
dc.date.available2023-08-02T11:13:06Z
dc.date.issued2022-02-27
dc.date.updated2023-07-03T09:05:45Z
dc.description.abstractImmune-related adverse events (irAEs) are frequent and could be associated with improved response to immune checkpoint inhibitors (ICIs). A prospective cohort of advanced melanoma patients receiving ICI as first-line therapy was retrospectively reviewed (January 2011-February 2019). A total of 116 of 153 patients presented with at least one irAE (75.8%). The most frequent irAEs were dermatological (derm irAEs, 50%), asthenia (38%), and gastrointestinal (29%). Most irAEs appeared within the first 90 days, while 11.2% appeared after discontinuation of the therapy. Mild grade 1-2 derm irAEs tended to appear within the first 2 months of therapy with a median time of 65.5 days (IQR 26-139.25), while grade 3-4 derm irAEs appeared later (median 114 days; IQR 69-218) and could be detected at any time during therapy. Only derm irAE occurrence was related to improved survival (HR 6.46). Patients presenting derm irAEs showed better 5-year overall survival compared to those with no derm irAEs (53.1% versus 24.9%; p < 0.001). However, the difference was not significant when adjusting for the duration of therapy. In conclusion: the timeline of immune-related-AEs differs according to the organ involved. The (apparent) improved survival of patients who present derm AEs during immunotherapy could be partially explained by longer times under treatment.
dc.format.extent11 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina9300294
dc.identifier.issn2072-6694
dc.identifier.pmid35267545
dc.identifier.urihttps://hdl.handle.net/2445/201454
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/cancers14051237
dc.relation.ispartofCancers, 2022, vol. 14, num. 5, p. 1237
dc.relation.urihttps://doi.org/10.3390/cancers14051237
dc.rightscc by (c) Villa Crespo, Lorena et al., 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject.classificationMelanoma
dc.subject.classificationImmunoglobulines
dc.subject.otherMelanoma
dc.subject.otherImmunoglobulins
dc.titleTimeline of Adverse Events during Immune Checkpoint Inhibitors for Advanced Melanoma and Their Impacts on Survival
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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