Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/191216
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dc.contributor.authorPantano, Francesco-
dc.contributor.authorTramontana, Flavia-
dc.contributor.authorIuliani, Michele-
dc.contributor.authorLeanza, Giulia-
dc.contributor.authorSimonetti, Sonia-
dc.contributor.authorPiccoli, Alessandra-
dc.contributor.authorPaviglianiti, Annalisa-
dc.contributor.authorCortellini, Alessio-
dc.contributor.authorSpinelli, Gian Paolo-
dc.contributor.authorLongo, Umile Giuseppe-
dc.contributor.authorStrollo, Rocky-
dc.contributor.authorVincenzi, Bruno-
dc.contributor.authorTonini, Giuseppe-
dc.contributor.authorNapoli, Nicola-
dc.contributor.authorSantini, Daniele-
dc.date.accessioned2022-11-30T12:37:30Z-
dc.date.available2022-11-30T12:37:30Z-
dc.date.issued2022-10-27-
dc.identifier.issn2212-1374-
dc.identifier.urihttp://hdl.handle.net/2445/191216-
dc.description.abstractImmune checkpoint inhibitors (ICIs) has revolutionized the treatment of different advanced solid tumors, but most patients develop severe immune-related adverse events (irAEs). Although a bi-directional crosstalk between bone and immune systems is widely described, the effect of ICIs on the skeleton is poorly investigated. Here, we analyze the changes in plasma levels of type I collagen C-terminal telopeptide (CTX-I) and N-terminal propeptide of type I procollagen (PINP), reference makers of bone turnover, in patients treated with ICIs and their associ-ation with clinical outcome.A series of 44 patients affected by advanced non-small cell lung cancer or renal cell carcinoma, without bone metastases, and treated with ICIs as monotherapy were enrolled. CTX-I and PINP plasma levels were assessed at baseline and after 3 months of ICIs treatment by ELISA kits.A significant increase of CTX-I with a concomitant decreasing trend towards the reduction of PINP was observed after 3 months of treatment. Intriguingly, CTX-I increase was associated with poor prognosis in terms of treatment response and survival. These data suggest a direct relationship between ICIs treatment, increased osteoclast activity and potential fracture risk.Overall, this study reveals that ICIs may act as triggers for skeletal events, and if confirmed in larger pro-spective studies, it would identify a new class of skeletal-related irAEs.-
dc.format.extent6 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier BV-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.jbo.2022.100459-
dc.relation.ispartofJournal of Bone Oncology, 2022, vol. 37, p. 100459-
dc.relation.urihttps://doi.org/10.1016/j.jbo.2022.100459-
dc.rightscc by-nc-nd (c) Pantano, Francesco et al., 2022-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationMalalties dels ossos-
dc.subject.classificationMetàstasi-
dc.subject.otherBone diseases-
dc.subject.otherMetastasis-
dc.titleChanges in bone turnover markers in patients without bone metastases receiving immune checkpoint inhibitors: An exploratory analysis-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2022-11-28T15:55:29Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid36338920-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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