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Gene Expression Signature for Prediction of Golimumab Response in a Phase 2a Open-Label Trial of Patients With Ulcerative Colitis.
Telesco, Shannon E; Brodmerkel, Carrie; Zhang, Hongyan; Kim, Lilianne Lee-Lian; Johanns, Jewel; Mazumder, Abhijit; Li, Katherine; Baribaud, Frédéric; Curran, Mark; Strauss, Richard; Paxson, Bethany; Plevy, Scott; Davison, Timothy; Knight, Laura; Dibben, Sian; Schreiber, Stefan; Sandborn, William; Rutgeerts, Paul; Siegel, Corey A; Reinisch, Walter; Greenbaum, Linda E.
Afiliação
  • Telesco SE; Immunology Biomarker, Janssen Research and Development, LLC, Spring House, Pennsylvania. Electronic address: stelesco@its.jnj.com.
  • Brodmerkel C; Immunology Biomarker, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Zhang H; Clinical Biostatistics, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Kim LL; Clinical Biostatistics, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Johanns J; Clinical Biostatistics, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Mazumder A; R&D Operations, Janssen Diagnostics, Janssen Research and Development, LLC, Spring House, Pennsylvania (former); Companion Diagnostics, Oncology Biomarker Development, Genentech, South San Francisco, California.
  • Li K; Immunology Biomarker, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Baribaud F; Immunology Biomarker, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Curran M; Immunology Companion Diagnostics, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Strauss R; Translational Medicine Science, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Paxson B; Global Regulatory Affairs, Immunology, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Plevy S; Disease Area Stronghold, Inflammatory Bowel Diseases, Janssen Research and Development, LLC, Spring House, Pennsylvania.
  • Davison T; Bioinformatics and Biostatistics, Almac Group, Craigavon, United Kingdom.
  • Knight L; Internal Product Development, Almac Group, Craigavon, United Kingdom.
  • Dibben S; Bioinformatics and Biostatistics, Almac Group, Craigavon, United Kingdom.
  • Schreiber S; Institute for Clinical Molecular Biology, Kiel, Germany.
  • Sandborn W; Department of Medicine, University of California San Diego, La Jolla, California.
  • Rutgeerts P; Department of Gastroenterology, University of Leuven, Leuven, Belgium.
  • Siegel CA; The Dartmouth Institute for Health Policy & Clinical Practice, Dartmouth-Hitchcock Inflammatory Bowel Disease Center, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Reinisch W; Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
  • Greenbaum LE; Clinical Development, Gastrointestinal, Immunology, Janssen Research and Development, LLC, Spring House, Pennsylvania (former); Novartis Institutes for Biomedical Research, East Hanover, New Jersey.
Gastroenterology ; 155(4): 1008-1011.e8, 2018 10.
Article em En | MEDLINE | ID: mdl-29981298
ABSTRACT
Golimumab, a tumor necrosis factor antagonist, is an effective treatment for patients with moderate-to-severe ulcerative colitis (UC); however, more than 50% of initial responders lose their response to the drug within the first year of therapy. A gene expression signature identified in colon biopsies collected before treatment was associated with response to infliximab, and was subsequently refined to associate with mucosal healing in response to golimumab. We performed a phase 2a open-label study of 103 golimumab-treated patients with moderate-to-severe UC to test whether the baseline gene expression signature could be used to predict which patients would achieve mucosal healing, clinical response, and clinical remission at weeks 6 and 30 of treatment. The gene expression signature identified patients who went on to achieve mucosal healing at treatment week 6 with an area under the receiver operating characteristic curve (AUCROC) of 0.688 (P = .002) and at week 30 with an AUCROC of 0.671 (P = .006). The signature identified patients with mucosal healing with 87% sensitivity, but only 34% specificity, limiting its clinical utility. The baseline gene expression signature did not identify patients who went on to achieve clinical remission or clinical response with statistical significance. Further studies are needed to identify biomarkers that can be used to predict which patients with UC will respond to treatment with anti-tumor necrosis factor agents. ClinicalTrials.gov no NCT01988961.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Colite Ulcerativa / Colo / Perfilação da Expressão Gênica / Transcriptoma / Mucosa Intestinal / Anti-Inflamatórios / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Gastroenterology Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Colite Ulcerativa / Colo / Perfilação da Expressão Gênica / Transcriptoma / Mucosa Intestinal / Anti-Inflamatórios / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Gastroenterology Ano de publicação: 2018 Tipo de documento: Article