Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23575
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dc.contributor.authorLasocki, Arian-
dc.contributor.authorKee, Damien-
dc.date2020-06-23-
dc.date.accessioned2020-06-30T04:09:50Z-
dc.date.available2020-06-30T04:09:50Z-
dc.date.issued2020-12-
dc.identifier.citationMelanoma research 2020; 30(6): 608-612-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23575-
dc.description.abstractImmune-related adverse events (irAEs) are a frequent complication of immunotherapy, but neurological irAEs are rare and varied. Here, we present a case of cerebral amyloid angiopathy-related inflammation (CAA-ri) attributable to nivolumab monotherapy, which has not been previously reported. The context of immunotherapy and availability of serial imaging also provide unique insights into the pathogenesis and evolution of CAA-ri. Routine surveillance neuroimaging in a patient with metastatic melanoma, in remission after treatment with nivolumab, demonstrated progressive microhaemorrhages and associated oedema, suspicious for CAA-ri. These changes progressed despite cessation of nivolumab. The patient was initially asymptomatic, but later developed an acute confusional state, warranting brain biopsy, which confirmed the diagnosis of CAA-ri. Treatment with methylprednisolone resulted in resolution of the oedema, and a marked decrease in the subsequent accumulation of microhaemorrhages. The temporal evolution prior to symptom development and subsequently related to treatment suggests that inflammation may be an important component of the pathogenesis of CAA-ri, rather than simply a secondary response. Given that immunotherapy is in its relative infancy, it is important to consider rare irAEs in patients exhibiting unusual imaging findings.-
dc.language.isoeng-
dc.titleClinical and radiological evolution of cerebral amyloid angiopathy-related inflammation in the context of anti-PD-1 immunotherapy.-
dc.typeJournal Article-
dc.identifier.journaltitleMelanoma research-
dc.identifier.affiliationDepartment of Medical Oncology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourneen
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Parkvilleen
dc.identifier.affiliationDepartment of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourneen
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, The University of Melbourne, Parkvilleen
dc.identifier.doi10.1097/CMR.0000000000000683-
dc.identifier.pubmedid32590413-
dc.type.austinJournal Article-
local.name.researcherKee, Damien
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptMedical Oncology-
Appears in Collections:Journal articles
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