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Clinical Trial
. 2020 Jan;72(1):125-136.
doi: 10.1002/art.41055. Epub 2019 Dec 10.

Abatacept in Early Diffuse Cutaneous Systemic Sclerosis: Results of a Phase II Investigator-Initiated, Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial

Dinesh Khanna  1 , Cathie Spino  1 , Sindhu Johnson  2 , Lorinda Chung  3 , Michael L Whitfield  4 , Christopher P Denton  5 , Veronica Berrocal  1 , Jennifer Franks  4 , Bhavan Mehta  4 , Jerry Molitor  6 , Virginia D Steen  7 , Robert Lafyatis  8 , Robert W Simms  9 , Anna Gill  5 , Suzanne Kafaja  10 , Tracy M Frech  11 , Vivien Hsu  12 , Robyn T Domsic  13 , Janet E Pope  14 , Jessica K Gordon  15 , Maureen D Mayes  16 , Elena Schiopu  1 , Amber Young  1 , Nora Sandorfi  17 , Jane Park  18 , Faye N Hant  19 , Elana J Bernstein  20 , Soumya Chatterjee  21 , Flavia V Castelino  22 , Ali Ajam  23 , Yue Wang  4 , Tammara Wood  4 , Yannick Allanore  24 , Marco Matucci-Cerinic  25 , Oliver Distler  26 , Ora Singer  1 , Erica Bush  1 , David A Fox  1 , Daniel E Furst  27
Affiliations
Clinical Trial

Abatacept in Early Diffuse Cutaneous Systemic Sclerosis: Results of a Phase II Investigator-Initiated, Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial

Dinesh Khanna et al. Arthritis Rheumatol. 2020 Jan.

Abstract

Objective: T cells play a key role in the pathogenesis of early systemic sclerosis. This study was undertaken to assess the safety and efficacy of abatacept in patients with diffuse cutaneous systemic sclerosis (dcSSc).

Methods: In this 12-month, randomized, double-blind, placebo-controlled trial, participants were randomized 1:1 to receive either subcutaneous abatacept 125 mg or matching placebo, stratified by duration of dcSSc. Escape therapy was allowed at 6 months for worsening disease. The coprimary end points were change in the modified Rodnan skin thickness score (MRSS) compared to baseline and safety over 12 months. Differences in longitudinal outcomes were assessed according to treatment using linear mixed models, with outcomes censored after initiation of escape therapy. Skin tissue obtained from participants at baseline was classified into intrinsic gene expression subsets.

Results: Among 88 participants, the adjusted mean change in the MRSS at 12 months was -6.24 units for those receiving abatacept and -4.49 units for those receiving placebo, with an adjusted mean treatment difference of -1.75 units (P = 0.28). Outcomes for 2 secondary measures (Health Assessment Questionnaire disability index and a composite measure) were clinically and statistically significantly better with abatacept. The proportion of subjects in whom escape therapy was needed was higher in the placebo group relative to the abatacept group (36% versus 16%). In the inflammatory and normal-like skin gene expression subsets, decline in the MRSS over 12 months was clinically and significantly greater in the abatacept group versus the placebo group (P < 0.001 and P = 0.03, respectively). In the abatacept group, adverse events occurred in 35 participants versus 40 participants in the placebo group, including 2 deaths and 1 death, respectively.

Conclusion: In this phase II trial, abatacept was well-tolerated, but change in the MRSS was not statistically significant. Secondary outcome measures, including gene expression subsets, showed evidence in support of abatacept. These data should be confirmed in a phase III trial.

Trial registration: ClinicalTrials.gov NCT02161406.

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Conflict of interest statement

Conflicts of interest:

Dr Khanna is a consultant to Actelion, Acceleron, Arena, Bayer, Boehringer Ingelheim, Bristol-Myer Squibb, CSL Behring, Corbus, Cytori, GSK, Genentech/Roche, Galapagos, Merck, Mitsubishi Tanabi, and UCB; he has received grants as part of investigator-initiated trials (to the University of Michigan) from Bayer, Bristol-Myer Squibb, and Pfizer; and has stock options in Eicos Sciences, Inc and employment with Civi BioPharma, Inc. Dr. Chung is a consultant to Reata, Bristol-Myer Squibb, Boehringer Ingelheim, Mitsubishi Tanabe, Eicos Sciences, Inc. Dr. Chung has also received grants from United Therapeutics. Dr. Molitor is a consultant to Boehringer-Ingelheim and Amgen. He has also received grants from Pfizer. Dr. Lafyatis is a consultant to PRISM Biolab, Merck, Bristol Myers Squibb, Biocon, UCB, Formation, Sanofi, and Genentech/Roche. He has received grants from PRISM Biolab, Regeneron, Elpidera, and Kiniksa. Dr. Domsic is a consultant to Eicos Sciences Inc. and Boehringer-Ingelheim. Dr. Pope is a consultant for Actelion, Baxter, Bristol-Myer Squibb, Merck, and Roche. She has received research grants from Baxter, Bristol-Myer Squibb, Eicos Sciences Inc, Merck, Roche, and Seattle Genetics. Dr. Gordon has received grants from Corbus and Cumberland Pharmaceuticals. Dr. Schiopu has received research grants from Bristol-Myer Squibb and Bayer. Dr. Bernstein is a consultant to Genentech as a medical monitor for SLS III. She has also received grants for investigator-initiated research from Pfizer and ASPIRE Rheumatology program. Dr. Castelino is a consultant to Genentech and Boehringer. Dr. Allanore is a consultant to BMS, Genentech/Roche, Sanofi, Bayer, Actelion, and Inventiva. Dr. Allanore has also received grants from Genentech/Roche, Sanofi, and Inventiva. Dr. Matucci-Cerinic is a consultant and has received grants from Bristol-Myer Squibb. Dr. Fox is a consultant as a grant reviewer for Pfizer. He has also received research grants from Regeneron, Gilead, and Seattle Genetics. Drs. Spino, Johnson, Whitfield, Berrocal, Franks, Mehta, Steen, Simms, Gill, Kafaja, Frech, Hsu, Mayes, Young, Sandorfi, Park, Hant, Chatterjee, Ajam, Wang, Wood, Distler, Singer, Bush, and Furst report no conflict of interest pertinent to this manuscript.

Figures

Figure 1:
Figure 1:
Enrollment of Participants and Study Flow
Figure 2:
Figure 2:
Change in the modified Rodnan skin score during 12-month period
Figure 3:
Figure 3:
Observed average change (left panels) and estimated average change from baseline in MRSS, FVC% and HAQ-DI (right panels) in the Placebo and Abatacept group and in the three intrinsic gene expression subsets. In each plot, vertical bars represent +/− 1 standard error. Estimates are obtained from a linear mixed model fitted to the change from baseline in MRSS, FVC% and HAQ-DI, respectively, with predictors: MRSS, FVC% and HAQ-DI at baseline, respectively, month in the study, treatment group, interaction of treatment group and month and a subject-specific random effect.
See this image and copyright information in PMC

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