Show simple item record

FieldValueLanguage
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_AU
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_AU
dc.language.isoenen_AU
dc.publisherWileyen_AU
dc.relation.ispartofPigment Cell and Melanoma Researchen_AU
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_AU
dc.typeArticleen_AU
dc.identifier.doi10.1111/pcmr.12340
dc.type.pubtypeAuthor accepted manuscripten_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Healthen_AU
usyd.departmentMelanoma Institute Australiaen_AU
usyd.citation.volume28en_AU
usyd.citation.issue3en_AU
usyd.citation.spage245en_AU
usyd.citation.epage253en_AU
workflow.metadata.onlyNoen_AU


Show simple item record

Associated file/s

Associated collections

Show simple item record

There are no previous versions of the item available.