<scp>PD</scp> ‐L1 expression in melanoma shows marked heterogeneity within and between patients: implications for anti‐ <scp>PD</scp> ‐1/ <scp>PD</scp> ‐ <scp>L</scp> 1 clinical trials

Jason Madore(The University of Sydney), Ricardo E. Vilain(The University of Sydney), Alexander M. Menzies(The University of Sydney), Hojabr Kakavand(The University of Sydney), James S. Wilmott(The University of Sydney), Jessica Hyman(Melanoma Institute Australia), Jennifer H. Yearley(Merck & Co., Inc., Rahway, NJ, USA (United States)), Richard Kefford(The University of Sydney), John F. Thompson(The University of Sydney), Georgina V. Long(The University of Sydney), Peter Hersey(The University of Sydney), Richard A. Scolyer(The University of Sydney)
Pigment Cell & Melanoma Research
December 8, 2014
Cited by 391

Abstract

This study evaluated the expression of PD-L1 in immunotherapy-naïve 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.


Related Papers

No related papers found

Powered by citation graph analysis