Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/201454
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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, Josep-
dc.contributor.authorPuig, Susana-
dc.contributor.authorCarrera, Cristina-
dc.date.accessioned2023-08-02T11:13:06Z-
dc.date.available2023-08-02T11:13:06Z-
dc.date.issued2022-02-27-
dc.identifier.issn2072-6694-
dc.identifier.urihttp://hdl.handle.net/2445/201454-
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.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.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-
dc.date.updated2023-07-03T09:05:45Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina9300294-
dc.identifier.pmid35267545-
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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