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Home » Meeting Abstracts » ACR/ARHP Annual Meeting 2017

Abstract Number: 2450

Comparative Effectiveness of Abatacept Versus TNFi in Patients with RA Who Are CCP+ in the United States Corrona Registry

Leslie R Harrold1, Heather J. Litman2, SE Connolly3, E Alemao3, K Price3, S Kelly3, Sabrina Rebello4, W Hua2 and Joel Kremer5, 1University of Massachusetts, Worcester, MA, 2Corrona, Southborough, MA, 3Bristol-Myers Squibb, Princeton, NJ, 4Corrona, LLC, Southborough, MA, 5Albany Medical College and The Center for Rheumatology, Albany, NY

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Meeting: ACR/ARHP Annual Meeting 2017

Date of first publication: September 18, 2017

Keywords: Abatacept, ACPA, rheumatoid arthritis (RA) and tumor necrosis factor (TNF)

Session Information

Date: Tuesday, November 7, 2017

Title: Rheumatoid Arthritis – Small Molecules, Biologics and Gene Therapy Poster III: Efficacy and Safety of Originator Biologics and Biosimilars

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Anti-cyclic citrullinated peptide positivity (CCP+) is associated with a better response to abatacept than anti-CCP negativity in patients with RA1,2; however, there are no head-to-head or comparative effectiveness research studies available evaluating responses to biologics in CCP+ patients in a real-world setting. The aim of this study was to compare the effectiveness of abatacept vs a TNF inhibitor (TNFi) in patients with RA who are CCP+. Methods: We identified adult patients with RA from a large observational US cohort (Dec 1, 2005–Aug 31, 2016) who initiated abatacept or a TNFi and who were CCP+ (≥20 U/mL) at or prior to initiation. Both groups had to have no prior exposure to other non-TNFi biologics or targeted synthetic DMARDs. TNFi initiators were excluded if they had prior use of abatacept. Using propensity score matching (1:1) stratified by prior TNFi use (0, 1 and 2+), effectiveness at 6 months after initiation was evaluated. Mean change in CDAI over 6 months following initiation was the primary outcome and secondary outcomes were: achievement of remission (CDAI ≤2.8), modified (m)ACR20, 50 and 70 responses and achievement of LDA/remission (CDAI ≤10) in those with moderate/high disease activity at initiation. A subset analysis was performed to consider separately patients who were biologic naïve and those who were biologic experienced at initiation.

Results: The 330 pairs of propensity score-matched abatacept and TNFi initiators had no substantial differences in baseline characteristics. Both treatment groups had similar mean change in CDAI at 6 months as well as achievement of LDA, remission and mACR20/50/70 responses (Table). Among the 97 matched biologic-naïve pairs, there was no significant difference in change in CDAI for abatacept initiators vs TNFi initiators (p=0.19). However, in the 233 matched biologic-experienced pairs, those initiating abatacept had a greater improvement in mean change in CDAI (p=0.033) and were more likely to achieve an mACR50 response (p=0.014).

Conclusion: Patients with RA who were CCP+ and received either abatacept or TNFi had a substantial improvement in clinical disease activity. In the overall propensity score-matched sample, similar outcomes were observed for both treatment groups. However, analysis of the biologic-experienced cohort found that abatacept initiators had a greater improvement in disease activity than TNFi initiators.

1. Sokolove J, et al. Ann Rheum Dis 2016;75:709–14.

2. Harrold LR, et al. Ann Rheum Dis 2016;75(Suppl 2):505–6.

Original abstract © EULAR/BMJ. First presented at EULAR 2017 and published in Ann Rheum Dis 2017;76 (Suppl 2):AB0408. Any reprints, promotional options, education material etc have to be done through the original source (ARD/BMJ).
Table


Disclosure: L. R. Harrold, Corrona, 1,Pfizer Inc, 2,Roche Pharmaceuticals, 5,Corrona, 3; H. J. Litman, Corrona, 3; S. Connolly, Bristol-Myers Squibb, 3,Bristol-Myers Squibb, 1; E. Alemao, Bristol-Myers Squibb, 3,Bristol-Myers Squibb, 1; K. Price, Bristol-Myers Squibb, 3,Bristol-Myers Squibb, 1; S. Kelly, Bristol-Myers Squibb, 3,Bristol-Myers Squibb, 1; S. Rebello, Corrona, 3; W. Hua, Corrona, 3; J. Kremer, Corrona, 1,AbbVie, BMS, Genentech, Lilly, Novartis, Pfizer, 2,Corrona, 3,Genentech and Biogen IDEC Inc., 8.

To cite this abstract in AMA style:

Harrold LR, Litman HJ, Connolly S, Alemao E, Price K, Kelly S, Rebello S, Hua W, Kremer J. Comparative Effectiveness of Abatacept Versus TNFi in Patients with RA Who Are CCP+ in the United States Corrona Registry [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/comparative-effectiveness-of-abatacept-versus-tnfi-in-patients-with-ra-who-are-ccp-in-the-united-states-corrona-registry/. Accessed .

ACR Meeting Abstracts - https://acrabstracts.org/abstract/comparative-effectiveness-of-abatacept-versus-tnfi-in-patients-with-ra-who-are-ccp-in-the-united-states-corrona-registry/

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