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dc.contributor.authorMadore, Jason
dc.contributor.authorVilain, Ricardo
dc.contributor.authorMenzies, Alexander M.
dc.contributor.authorKakavand, Hojabr
dc.contributor.authorWilmott, James S.
dc.contributor.authorHyman, Jessica
dc.contributor.authorYearley, Jennifer H.
dc.contributor.authorKefford, Richard F.
dc.contributor.authorThompson, John Francis
dc.contributor.authorLong, Georgina V.
dc.contributor.authorHersey, Peter
dc.contributor.authorScolyer, Richard A.
dc.date.accessioned2025-02-19T22:33:02Z
dc.date.available2025-02-19T22:33:02Z
dc.date.issued2015en
dc.identifier.urihttps://hdl.handle.net/2123/33649
dc.description.abstractThis study evaluated the expression of PD-L1 in immunotherapy-naive metastatic melanoma patients to determine longitudinal intrapatient concordance and correlate PD-L1 status with clinicopathologic characteristics and outcome. PD-L1 expression was assessed by immunohistochemistry in 58 patients (43 primary tumors, 96 metastases). Seventy-two percent of patients had at least one specimen expressing PD-L1 in >/= 1% of tumor cells. Median positive tumor cell count overall was low (8% in nonzero specimens). PD-L1 expression was frequently discordant between primary tumors and metastases and between intrapatient metastases, such that 23/46 longitudinal patient specimens were discordant. PD-L1 was associated with higher TIL grade but not with other known prognostic features. There was a positive univariate association between PD-L1 expression in locoregional metastases and melanoma-specific survival, but the effect was not observed for primary melanoma. In locoregional lymph node metastasis, PD-L1+/TIL+ patients had the best outcome, and PD-L1+/TIL- patients had poor outcome.en
dc.language.isoenen
dc.publisherWileyen
dc.relation.ispartofPigment Cell and Melanoma Researchen
dc.rightsOther
dc.titlePD-L1 expression in melanoma has prognostic significance but shows marked heterogeneity within and between patients- implications for anti-PD-1/PD-L1 clinical trialsen
dc.typeArticleen
dc.identifier.doi10.1111/pcmr.12340
dc.type.pubtypeAuthor accepted manuscripten
usyd.facultySeS faculties schools::Faculty of Medicine and Healthen
usyd.departmentMelanoma Institute Australiaen
usyd.citation.volume28en
usyd.citation.issue3en
usyd.citation.spage245en
usyd.citation.epage253en
workflow.metadata.onlyNoen


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