{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Slingluff CL"],"funding":["NCRR NIH HHS","NCI NIH HHS"],"pagination":["2924-32"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3138719"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["29(21)"],"pubmed_abstract":["<h4>Purpose</h4>This multicenter randomized trial was designed to test whether melanoma-associated helper peptides augment CD8(+) T-cell responses to a melanoma vaccine and whether cyclophosphamide (CY) pretreatment augments CD4(+) or CD8(+) T-cell responses to that vaccine.<h4>Patients and methods</h4>In all, 167 eligible patients with resected stage IIB to IV melanoma were randomly assigned to four vaccination study arms. Patients were vaccinated with 12 class I major histocompatibility complex-restricted melanoma peptides (12MP) to stimulate CD8(+) T cells and were randomly assigned to receive a tetanus helper peptide or a mixture of six melanoma-associated helper peptides (6MHP) to stimulate CD4(+) T cells. Before vaccination, patients were also randomly assigned to receive CY pretreat"],"journal":["Journal of clinical oncology : official journal of the American Society of Clinical Oncology"],"pubmed_title":["Randomized multicenter trial of the effects of melanoma-associated helper peptides and cyclophosphamide on the immunogenicity of a multipeptide melanoma vaccine."],"pmcid":["PMC3138719"],"funding_grant_id":["M01 RR000847","P30 CA44579","R01 CA118386","M01 RR00847","P30 CA044579"],"pubmed_authors":["von Mehren M","Chianese-Bullock KA","Smolkin ME","Haas NB","Ross MI","Petroni GR","Slingluff CL","Grosh WW"],"additional_accession":[]},"is_claimable":false,"name":"Randomized multicenter trial of the effects of melanoma-associated helper peptides and cyclophosphamide on the immunogenicity of a multipeptide melanoma vaccine.","description":"<h4>Purpose</h4>This multicenter randomized trial was designed to test whether melanoma-associated helper peptides augment CD8(+) T-cell responses to a melanoma vaccine and whether cyclophosphamide (CY) pretreatment augments CD4(+) or CD8(+) T-cell responses to that vaccine.<h4>Patients and methods</h4>In all, 167 eligible patients with resected stage IIB to IV melanoma were randomly assigned to four vaccination study arms. Patients were vaccinated with 12 class I major histocompatibility complex-restricted melanoma peptides (12MP) to stimulate CD8(+) T cells and were randomly assigned to receive a tetanus helper peptide or a mixture of six melanoma-associated helper peptides (6MHP) to stimulate CD4(+) T cells. Before vaccination, patients were also randomly assigned to receive CY pretreat","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Jul","modification":"2026-05-04T18:39:02.455Z","creation":"2019-03-26T23:49:33Z"},"accession":"S-EPMC3138719","cross_references":{"pubmed":["21690475"],"doi":["10.1200/jco.2010.33.8053","10.1200/JCO.2010.33.8053"]}}