<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Giraldo NA</submitter><funding>Bloomberg~Kimmel Institute for Cancer Immunotherapy, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University</funding><funding>Bristol-Myers Squibb</funding><funding>Stand Up To Cancer–Cancer Research Institute Cancer Immunology Translational Cancer Research Grant</funding><funding>Cancer Immunotherapy Trials Network</funding><funding>Melanoma Research Alliance</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>Sidney Kimmel Comprehensive Cancer Center</funding><pagination>99</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6167897</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>We recently reported a 56% objective response rate in patients with advanced Merkel cell carcinoma (MCC) receiving pembrolizumab. However, a biomarker predicting clinical response was not identified.&lt;h4>Methods&lt;/h4>Pretreatment FFPE tumor specimens (n = 26) were stained for CD8, PD-L1, and PD-1 by immunohistochemistry/immunofluorescence (IHC/IF), and the density and distribution of positive cells was quantified to determine the associations with anti-PD-1 response. Multiplex IF was used to test a separate cohort of MCC archival specimens (n = 16), to identify cell types expressing PD-1.&lt;h4>Results&lt;/h4>Tumors from patients who responded to anti-PD-1 showed higher densities of PD-1+ and PD-L1+ cells when compared to non-responders (median cells/mm&lt;sup>2&lt;/sup>, 70.7 vs. 6.7</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>Multidimensional, quantitative assessment of PD-1/PD-L1 expression in patients with Merkel cell carcinoma and association with response to pembrolizumab.</pubmed_title><pmcid>PMC6167897</pmcid><funding_grant_id>SU2C-AACR-DT1012</funding_grant_id><funding_grant_id>P30 CA006973</funding_grant_id><funding_grant_id>IH/NCI Cancer Center Support Grant P30 CA015704</funding_grant_id><funding_grant_id>P30 CA015704</funding_grant_id><funding_grant_id>UM1 CA154967</funding_grant_id><funding_grant_id>T32 CA193145</funding_grant_id><funding_grant_id>K24 CA139052</funding_grant_id><funding_grant_id>R01 CA142779</funding_grant_id><pubmed_authors>Anders RA</pubmed_authors><pubmed_authors>Cheever M</pubmed_authors><pubmed_authors>Nghiem PT</pubmed_authors><pubmed_authors>Sunshine JC</pubmed_authors><pubmed_authors>Danilova L</pubmed_authors><pubmed_authors>Kaunitz GJ</pubmed_authors><pubmed_authors>Lipson EJ</pubmed_authors><pubmed_authors>Fling S</pubmed_authors><pubmed_authors>Berry S</pubmed_authors><pubmed_authors>Giraldo NA</pubmed_authors><pubmed_authors>Church CD</pubmed_authors><pubmed_authors>Succaria F</pubmed_authors><pubmed_authors>Taube JM</pubmed_authors><pubmed_authors>Lundgren L</pubmed_authors><pubmed_authors>Green B</pubmed_authors><pubmed_authors>Ogurtsova A</pubmed_authors><pubmed_authors>Soni A</pubmed_authors><pubmed_authors>Yearley JH</pubmed_authors><pubmed_authors>Nguyen P</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Engle EL</pubmed_authors><pubmed_authors>Miller NJ</pubmed_authors><pubmed_authors>Ramchurren N</pubmed_authors><pubmed_authors>Stein JE</pubmed_authors><pubmed_authors>Cuda JD</pubmed_authors><pubmed_authors>Cottrell TR</pubmed_authors><pubmed_authors>Topalian SL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multidimensional, quantitative assessment of PD-1/PD-L1 expression in patients with Merkel cell carcinoma and association with response to pembrolizumab.</name><description>&lt;h4>Background&lt;/h4>We recently reported a 56% objective response rate in patients with advanced Merkel cell carcinoma (MCC) receiving pembrolizumab. However, a biomarker predicting clinical response was not identified.&lt;h4>Methods&lt;/h4>Pretreatment FFPE tumor specimens (n = 26) were stained for CD8, PD-L1, and PD-1 by immunohistochemistry/immunofluorescence (IHC/IF), and the density and distribution of positive cells was quantified to determine the associations with anti-PD-1 response. Multiplex IF was used to test a separate cohort of MCC archival specimens (n = 16), to identify cell types expressing PD-1.&lt;h4>Results&lt;/h4>Tumors from patients who responded to anti-PD-1 showed higher densities of PD-1+ and PD-L1+ cells when compared to non-responders (median cells/mm&lt;sup>2&lt;/sup>, 70.7 vs. 6.7</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2025-04-22T12:55:08.892Z</modification><creation>2019-03-26T23:59:42Z</creation></dates><accession>S-EPMC6167897</accession><cross_references><pubmed>30285852</pubmed><doi>10.1186/s40425-018-0404-0</doi></cross_references></HashMap>