Cargando…
Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial
OBJECTIVES: To examine whether baseline anti-cyclic citrullinated peptide-2 (CCP2) antibody status and concentration correlated with clinical outcomes in patients treated with abatacept or adalimumab on background methotrexate (MTX) in the 2-year AMPLE (Abatacept versus adaliMumab comParison in bioL...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819608/ https://www.ncbi.nlm.nih.gov/pubmed/26359449 http://dx.doi.org/10.1136/annrheumdis-2015-207942 |
_version_ | 1782425239917953024 |
---|---|
author | Sokolove, Jeremy Schiff, Michael Fleischmann, Roy Weinblatt, Michael E Connolly, Sean E Johnsen, Alyssa Zhu, Jin Maldonado, Michael A Patel, Salil Robinson, William H |
author_facet | Sokolove, Jeremy Schiff, Michael Fleischmann, Roy Weinblatt, Michael E Connolly, Sean E Johnsen, Alyssa Zhu, Jin Maldonado, Michael A Patel, Salil Robinson, William H |
author_sort | Sokolove, Jeremy |
collection | PubMed |
description | OBJECTIVES: To examine whether baseline anti-cyclic citrullinated peptide-2 (CCP2) antibody status and concentration correlated with clinical outcomes in patients treated with abatacept or adalimumab on background methotrexate (MTX) in the 2-year AMPLE (Abatacept versus adaliMumab comParison in bioLogic-naïvE rheumatoid arthritis subjects with background MTX) study. METHODS: In this exploratory analysis, anti-CCP2 antibody concentration was measured at baseline, and antibody-positive patients were divided into equal quartiles, Q1–Q4, representing increasing antibody concentrations. Clinical outcomes analysed by baseline anti-CCP2 status and quartile included change from baseline in disease activity and disability and remission rates. RESULTS: Baseline characteristics were generally comparable across quartiles and treatment groups. In both treatment groups, anti-CCP2 antibody-negative patients responded less well than antibody-positive patients. At year 2, improvements in disease activity and disability and remission rates were similar across Q1–Q3, but were numerically higher in Q4 in the abatacept group; in contrast, treatment effects were similar across all quartiles in the adalimumab group. CONCLUSIONS: In AMPLE, baseline anti-CCP2 positivity was associated with a better response for abatacept and adalimumab. Patients with the highest baseline anti-CCP2 antibody concentrations had better clinical response with abatacept than patients with lower concentrations, an association that was not observed with adalimumab. TRIAL REGISTRATION NUMBER: NCT00929864. |
format | Online Article Text |
id | pubmed-4819608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48196082016-04-19 Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial Sokolove, Jeremy Schiff, Michael Fleischmann, Roy Weinblatt, Michael E Connolly, Sean E Johnsen, Alyssa Zhu, Jin Maldonado, Michael A Patel, Salil Robinson, William H Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVES: To examine whether baseline anti-cyclic citrullinated peptide-2 (CCP2) antibody status and concentration correlated with clinical outcomes in patients treated with abatacept or adalimumab on background methotrexate (MTX) in the 2-year AMPLE (Abatacept versus adaliMumab comParison in bioLogic-naïvE rheumatoid arthritis subjects with background MTX) study. METHODS: In this exploratory analysis, anti-CCP2 antibody concentration was measured at baseline, and antibody-positive patients were divided into equal quartiles, Q1–Q4, representing increasing antibody concentrations. Clinical outcomes analysed by baseline anti-CCP2 status and quartile included change from baseline in disease activity and disability and remission rates. RESULTS: Baseline characteristics were generally comparable across quartiles and treatment groups. In both treatment groups, anti-CCP2 antibody-negative patients responded less well than antibody-positive patients. At year 2, improvements in disease activity and disability and remission rates were similar across Q1–Q3, but were numerically higher in Q4 in the abatacept group; in contrast, treatment effects were similar across all quartiles in the adalimumab group. CONCLUSIONS: In AMPLE, baseline anti-CCP2 positivity was associated with a better response for abatacept and adalimumab. Patients with the highest baseline anti-CCP2 antibody concentrations had better clinical response with abatacept than patients with lower concentrations, an association that was not observed with adalimumab. TRIAL REGISTRATION NUMBER: NCT00929864. BMJ Publishing Group 2016-04 2015-09-10 /pmc/articles/PMC4819608/ /pubmed/26359449 http://dx.doi.org/10.1136/annrheumdis-2015-207942 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Clinical and Epidemiological Research Sokolove, Jeremy Schiff, Michael Fleischmann, Roy Weinblatt, Michael E Connolly, Sean E Johnsen, Alyssa Zhu, Jin Maldonado, Michael A Patel, Salil Robinson, William H Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title | Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title_full | Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title_fullStr | Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title_full_unstemmed | Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title_short | Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial |
title_sort | impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the ample trial |
topic | Clinical and Epidemiological Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819608/ https://www.ncbi.nlm.nih.gov/pubmed/26359449 http://dx.doi.org/10.1136/annrheumdis-2015-207942 |
work_keys_str_mv | AT sokolovejeremy impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT schiffmichael impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT fleischmannroy impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT weinblattmichaele impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT connollyseane impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT johnsenalyssa impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT zhujin impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT maldonadomichaela impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT patelsalil impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial AT robinsonwilliamh impactofbaselineanticycliccitrullinatedpeptide2antibodyconcentrationonefficacyoutcomesfollowingtreatmentwithsubcutaneousabataceptoradalimumab2yearresultsfromtheampletrial |