<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pistillo MP</submitter><funding>Italian Minister of Health</funding><pagination>97-107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11028053</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>68(1)</volume><pubmed_abstract>CTLA-4 blockade by means of ipilimumab (IPI) potentiates the immune response and improves overall survival (OS) in a minority of metastatic melanoma (MM) patients. We investigated the role of soluble CTLA-4 (sCTLA-4) as a possible biomarker for identifying this subset of patients. sCTLA-4 levels were analyzed at baseline in sera from 113 IPI-treated MM patients by ELISA, and the median value (200 pg/ml) was used to create two equally sized subgroups. Associations of sCTLA-4 with best overall response (BOR) to IPI and immune-related adverse events (irAEs) were evaluated through logistic regression. Kaplan-Meier and Cox regression methods were used to analyze OS. A remarkable association between sCTLA-4 levels and BOR was found. Specifically, the proportion of patients with sCTLA-4 > 200 pg/ml in irSD or irPD (immune-related stable or progressive disease) was, respectively, 80% (OR = 0.23; 95%CL = 0.03-1.88) and 89% (OR = 0.11; 95%CL = 0.02-0.71) and was lower than that observed among patients in irCR/irPR (immune-related complete/partial response). sCTLA-4 levels increased during IPI treatment, since the proportion of patients showing sCTLA > 200 pg/ml after 3 cycles was 4 times higher (OR = 4.41, 95%CL = 1.02-19.1) than that after 1 cycle. Moreover, a significantly lower death rate was estimated for patients with sCTLA-4 > 200 pg/ml (HR = 0.61, 95%CL = 0.39-0.98). Higher baseline sCTLA-4 levels were also associated with the onset of any irAE (p value = 0.029), in particular irAEs of the digestive tract (p value = 0.041). In conclusion, our results suggest that high sCTLA-4 serum levels might predict favorable clinical outcome and higher risk of irAEs in IPI-treated MM patients.</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>Soluble CTLA-4 as a favorable predictive biomarker in metastatic melanoma patients treated with ipilimumab: an Italian melanoma intergroup study.</pubmed_title><pmcid>PMC11028053</pmcid><funding_grant_id>5x1000 (2013,2014)</funding_grant_id><pubmed_authors>Carosio R</pubmed_authors><pubmed_authors>De Galitiis F</pubmed_authors><pubmed_authors>Martinoli C</pubmed_authors><pubmed_authors>Simeone E</pubmed_authors><pubmed_authors>Queirolo P</pubmed_authors><pubmed_authors>Laurent S</pubmed_authors><pubmed_authors>Dozin B</pubmed_authors><pubmed_authors>Marchetti P</pubmed_authors><pubmed_authors>Banelli B</pubmed_authors><pubmed_authors>Pistillo MP</pubmed_authors><pubmed_authors>Pagani E</pubmed_authors><pubmed_authors>Cocorocchio E</pubmed_authors><pubmed_authors>Tommasi S</pubmed_authors><pubmed_authors>Antonini Cappellini GC</pubmed_authors><pubmed_authors>Ascierto PA</pubmed_authors><pubmed_authors>Quaglino P</pubmed_authors><pubmed_authors>Romani M</pubmed_authors><pubmed_authors>Ferrero F</pubmed_authors><pubmed_authors>Morabito A</pubmed_authors><pubmed_authors>Tanda E</pubmed_authors><pubmed_authors>Ferrucci PF</pubmed_authors><pubmed_authors>Osella-Abate S</pubmed_authors><pubmed_authors>Guida M</pubmed_authors><pubmed_authors>Spagnolo F</pubmed_authors><pubmed_authors>Italian Melanoma Intergroup (IMI)</pubmed_authors><pubmed_authors>Fava P</pubmed_authors><pubmed_authors>Capone M</pubmed_authors><pubmed_authors>Fontana V</pubmed_authors><pubmed_authors>Spano L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Soluble CTLA-4 as a favorable predictive biomarker in metastatic melanoma patients treated with ipilimumab: an Italian melanoma intergroup study.</name><description>CTLA-4 blockade by means of ipilimumab (IPI) potentiates the immune response and improves overall survival (OS) in a minority of metastatic melanoma (MM) patients. We investigated the role of soluble CTLA-4 (sCTLA-4) as a possible biomarker for identifying this subset of patients. sCTLA-4 levels were analyzed at baseline in sera from 113 IPI-treated MM patients by ELISA, and the median value (200 pg/ml) was used to create two equally sized subgroups. Associations of sCTLA-4 with best overall response (BOR) to IPI and immune-related adverse events (irAEs) were evaluated through logistic regression. Kaplan-Meier and Cox regression methods were used to analyze OS. A remarkable association between sCTLA-4 levels and BOR was found. Specifically, the proportion of patients with sCTLA-4 > 200 pg/ml in irSD or irPD (immune-related stable or progressive disease) was, respectively, 80% (OR = 0.23; 95%CL = 0.03-1.88) and 89% (OR = 0.11; 95%CL = 0.02-0.71) and was lower than that observed among patients in irCR/irPR (immune-related complete/partial response). sCTLA-4 levels increased during IPI treatment, since the proportion of patients showing sCTLA > 200 pg/ml after 3 cycles was 4 times higher (OR = 4.41, 95%CL = 1.02-19.1) than that after 1 cycle. Moreover, a significantly lower death rate was estimated for patients with sCTLA-4 > 200 pg/ml (HR = 0.61, 95%CL = 0.39-0.98). Higher baseline sCTLA-4 levels were also associated with the onset of any irAE (p value = 0.029), in particular irAEs of the digestive tract (p value = 0.041). In conclusion, our results suggest that high sCTLA-4 serum levels might predict favorable clinical outcome and higher risk of irAEs in IPI-treated MM patients.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-22T20:42:55.407Z</modification><creation>2025-04-06T03:14:36.646Z</creation></dates><accession>S-EPMC11028053</accession><cross_references><pubmed>30311027</pubmed><doi>10.1007/s00262-018-2258-1</doi></cross_references></HashMap>