<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sanmamed MF</submitter><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>1988-1995</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5834104</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Surrogate biomarkers of efficacy are needed for anti-PD1/PD-L1 therapy, given the existence of delayed responses and pseudo-progressions. We evaluated changes in serum IL-8 levels as a biomarker of response to anti-PD-1 blockade in melanoma and non-small-cell lung cancer (NSCLC) patients.&lt;h4>Patients and methods&lt;/h4>Metastatic melanoma and NSCLC patients treated with nivolumab or pembrolizumab alone or nivolumab plus ipilimumab were studied. Serum was collected at baseline; at 2-4 weeks after the first dose; and at the time-points of response evaluation. Serum IL-8 levels were determined by sandwich ELISA. Changes in serum IL-8 levels were compared with the Wilcoxon test and their strength of association with response was assessed with the Mann-Whitney test. Accuracy of </pubmed_abstract><journal>Annals of oncology : official journal of the European Society for Medical Oncology</journal><pubmed_title>Changes in serum interleukin-8 (IL-8) levels reflect and predict response to anti-PD-1 treatment in melanoma and non-small-cell lung cancer patients.</pubmed_title><pmcid>PMC5834104</pmcid><funding_grant_id>P50 CA121974</funding_grant_id><funding_grant_id>SAF2011-22831</funding_grant_id><funding_grant_id>SAF2014-52361-R</funding_grant_id><pubmed_authors>Morgado M</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Sznol M</pubmed_authors><pubmed_authors>Melero I</pubmed_authors><pubmed_authors>Perez-Gracia JL</pubmed_authors><pubmed_authors>Andueza MP</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Alfaro C</pubmed_authors><pubmed_authors>Martin-Algarra S</pubmed_authors><pubmed_authors>Bacchiocchi A</pubmed_authors><pubmed_authors>Schalper KA</pubmed_authors><pubmed_authors>Kluger H</pubmed_authors><pubmed_authors>Rodriguez-Ruiz ME</pubmed_authors><pubmed_authors>Fusco JP</pubmed_authors><pubmed_authors>Onate C</pubmed_authors><pubmed_authors>Halaban R</pubmed_authors><pubmed_authors>Sanmamed MF</pubmed_authors><pubmed_authors>Perez G</pubmed_authors><pubmed_authors>Gonzalez A</pubmed_authors><pubmed_authors>Gurpide A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Changes in serum interleukin-8 (IL-8) levels reflect and predict response to anti-PD-1 treatment in melanoma and non-small-cell lung cancer patients.</name><description>&lt;h4>Background&lt;/h4>Surrogate biomarkers of efficacy are needed for anti-PD1/PD-L1 therapy, given the existence of delayed responses and pseudo-progressions. We evaluated changes in serum IL-8 levels as a biomarker of response to anti-PD-1 blockade in melanoma and non-small-cell lung cancer (NSCLC) patients.&lt;h4>Patients and methods&lt;/h4>Metastatic melanoma and NSCLC patients treated with nivolumab or pembrolizumab alone or nivolumab plus ipilimumab were studied. Serum was collected at baseline; at 2-4 weeks after the first dose; and at the time-points of response evaluation. Serum IL-8 levels were determined by sandwich ELISA. Changes in serum IL-8 levels were compared with the Wilcoxon test and their strength of association with response was assessed with the Mann-Whitney test. Accuracy of </description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2025-04-19T15:18:08.534Z</modification><creation>2019-03-26T23:48:52Z</creation></dates><accession>S-EPMC5834104</accession><cross_references><pubmed>28595336</pubmed><doi>10.1093/annonc/mdx190</doi></cross_references></HashMap>