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Abstract Number: 520

Clinical and Structural Responses of Patients with Active Rheumatoid Arthritis (RA) Using Step-up Dosing of Tofacitinib in a Treat to Target Approach

Norman Gaylis1, Joanne Sagliani1 and Steven Needell2, 1Arthritis & Rheumatic Disease Specialties, Aventura, FL, 2Boca Radiology, Boca Raton, FL

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Biologic drugs and rheumatoid arthritis, treatment

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Session Information

Date: Sunday, November 5, 2017

Title: Rheumatoid Arthritis – Small Molecules, Biologics and Gene Therapy Poster I: Comorbidities and Adverse Events; Efficacy and Safety of Small Molecules

Session Type: ACR Poster Session A

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

Background/Purpose: Tofacitinib has been shown to reduce the clinical signs and symptoms of some RA patients at an approved dose of 5 mg bid. Studies report that 10 mg bid is an effective dose. This is the first community practice trial to measure the clinical and structural benefits of stepping up the initial dose of 5 mg bid in non-responders to 10 mg bid in order to achieve a clinical response using a treat to target approach.

Ojective:This study evaluates the optimal dose of tofacitinib (5 mg bid VS 10 mg bid) needed to reach treatment target in a cohort of patients with active RA while comparing the corresponding structural findings measured by low field MRI

Methods: 20 RA patients who were unresponsive to either methotrexate (10-25 mg weekly) or MTX plus up to 2 prior biologics with synovitis, osteitis or erosions on Baseline MRI (Esaote 0.3T) were treated with 5 mg bid tofacitinib with a treat to target goal of LDA or remission depending on the Clinical Activity Index (CDAI) score at Baseline. If the target was not met and sustained for 3 months, the dose of tofacitinib was increased to 10 mg bid in an attempt to reach target. MRIs of the hand/wrist were blindly read by a musculoskeletal radiologist using a RAMRIS score. A CDAI score of >10 was needed at study entry.

Results: Of the 20 enrolled patients, 6 remained at 5 mg bid and 14 were dose escalated to 10 mg bid most at the 12 week period. Of the 5 mg bid group, 3 completed the trial at target and 3 early termed (ET) for lack of efficacy, relocation and AE. Structurally, there was no change in erosions in all 3 patients; 2 showed regression of synovitis and 1 showed no change: 2 showed regression in osteitis and 1 no change. Of the 14 patients escalated to 10 mg bid, 11 completed the trial with 7 remissions, 2 at LDA, and 1 at MDA. 3 patients ET due to lack of efficacy. In the 10 mg bid group, 9 patients showed no change in erosions, 1 regression and 1 progression. 5 patients showed no change in synovitis and 6 showed regression, and 7 showed no change in osteitis, 3 showed regression and 1 showed progression. The CRP values correlated with the improvement of the clinical and structural results, in particular, the levels improved after the dose was increased to 10 mg bid.

Conclusion: Our results suggest that a significant number of patients treated with the standard dose of 5 mg bid may potentially have improved outcomes including LDA or remission when treated at a higher dose (10 mg bid). This is evidenced by the results of 11 of the 14 patients having significant improved response most after 3 months of treatment with 10 mg bid. Furthermore, the structural findings correlate in large part to the clinical findings showing stabilization or improvement in most patients. An extension trial is currently ongoing to determine if the positive outcome of LDA or remission at the higher dose (10 mg bid) can be sustained if the dose if reduced back down to 5 mg bid.


Patient

CDAI BSL

CDAI 3 Mnth

All taking 5 mg bid

CDAI 12 Mnth

Remain on

5 mg bid

CDAI 12 Mnth Dose Increased

10 mg bid

001

24.9

0.6

6

002

56.1

20.9

2.7

003

45.9

27.4

2.3

004

65.2

33.8

0

005

56.1

15.5

3.1

006

34.7

38.9

19.4

007

27.9

56

1.5

008

34.3

18.4

1.8

009

43.6

3.3

2.3

010

33.5

12.6

ET

011

32.7

5.1

ET

012

25.3

13

0

013

21.2

2.4

ET

014

21.6

9.9

2.9

015

21.6

5.2

ET

016

27.7

0.4

ET

018

31.8

16.9

2.1

019

27.3

0.9

5.2

020

14.5

5.2

ET

021

30.5

2.1

1.9


Disclosure: N. Gaylis, None; J. Sagliani, None; S. Needell, None.

To cite this abstract in AMA style:

Gaylis N, Sagliani J, Needell S. Clinical and Structural Responses of Patients with Active Rheumatoid Arthritis (RA) Using Step-up Dosing of Tofacitinib in a Treat to Target Approach [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/clinical-and-structural-responses-of-patients-with-active-rheumatoid-arthritis-ra-using-step-up-dosing-of-tofacitinib-in-a-treat-to-target-approach/. Accessed .
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