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Abstract Number: 455

Analysis of Real-World Treatment Patterns in a Matched Sample of Rheumatology Patients with Continuous Infliximab Therapy or Switched to Biosimilar Infliximab

Lorie A. Ellis1, Ismail Simsek2, Lin Xie3, Adesuwa Ogbomo3, Dennis Parenti4, Kavitha Goyal4 and Yusuf Yazici5, 1Janssen HECOR Immunology, Horsham, PA, 2Guven Hospital, Ankara, Turkey, 3STATinMED Research Inc., Ann Arbor, MI, 4Janssen Scientific Affairs, LLC, Horsham, PA, 5New York University School of Medicine, New York, NY

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: biosimilars, infliximab, rheumatoid arthritis (RA) and treatment

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Session Information

Date: Sunday, November 5, 2017

Title: Rheumatoid Arthritis – Clinical Aspects Poster I: Treatment Patterns and Response

Session Type: ACR Poster Session A

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

Background/Purpose: Biosimilar infliximab (CT-P13) was first approved in Europe in 2013.This study compared treatment (tx) patterns of Turkish pts with a diagnosis of rheumatoid arthritis(RA) who initiated originator IFX(IFX) & either continued IFX or switched to CT-P13.

Methods: Adult pts with ≥1 RA diagnosis code & IFX claim were identified in a national Turkish healthcare database. Eligible pts initiated & continued IFX (Continuer cohort; CC) or initiated IFX & switched to CT-P13 (Switch cohort; SC) during the study period (01DEC2010-01JUN2016). The index date was defined as CT-P13 switch date for SC or a random IFX date during period of CT-P13 availability for CC. Cohorts were matched on age,sex,&number of IFX prescriptions during baseline(BL).  Discontinuation (d/c) was defined as a switch to another biologic or no index biologic for ≥120 days without censoring.  Pt demographics, d/c & switching were summarized with descriptive statistics.

Results: A total of 697 pts initiating IFX were studied; 87%(N=605) continued IFX throughout the study period; 13%(N=92) switched to CT-P13. BL & clinical characteristics are shown in Table. Mean duration of IFX therapy during BL period was 422 days(CC) & 438 days(SC). Average duration of post-index follow-up was 16 months(CC) & 15 months(SC). During the combined BL & post-index periods, median time on any IFX therapy was 1080 days(CC)&540 days(SC)(Figure).D/c post-index occurred in 19%(CC) & 87%(SC); mean time from index to IFX d/c /censoring was 276 days(CC) while mean time from index to CT-P13 d/c /censoring was 132 days.While switching from IFX to CT-P13 occurred in 13% all IFX initiators on the index date; an additional 10% of the CC switched to a non-IFX anti-TNF post-index. The majority of SC(82%) switched again post-index (off CT-P13) & 88% of those re-initiated IFX. Regional variation in switching was noted. Switching from IFX to CT-P13 occurred most frequently in Central Anatolia (26% of 154 IFX initiators).Switching from CT-P13 occurred in >75% of SC pts in all regions except for Aegean(44% switched from CT-P13 to another biologic, predominantly IFX).

Conclusion: In Turkey, RA pts maintained on IFX had greater tx persistence than those who initiated IFX & switched to CT-P13. CT-P13 d/c resulted in IFX re-initiation in the majority of pts. Reasons for d/c are unknown, however regional differences in practice patterns were observed.

 

 

Table Demographics and Treatment Patterns for Continuer and Switcher Cohorts

 

Continuers Cohort

Switchers Cohort

(N=605)

(N=92)

N/Mean

%/SD

N/Mean

%/SD

Age (Mean) (years)

41

10.3

43

11.8

Sex

Women

309

51%

48

52%

Baseline Concomitant Disease

Ankylosing Spondylitis

102

18%

27

13%

Psoriatic Arthritis

48

8%

11

5%

Crohn’s Disease

244

42%

114

56%

Ulcerative Colitis

42

7%

9

4%

Average Length of Follow-up Period (months)

16

2

15

2

Post-Index Concomitant Disease

Ankylosing Spondylitis

363

60%

58

63%

Psoriatic Arthritis

102

17%

13

14%

Crohn’s Disease

48

8%

3

3%

Ulcerative Colitis

33

5%

4

4%

Switching

N and % of patients with  ≥1  switch

115

19%

75

82%

N and % Primary Switches from CT-P13 to IFX

NA

NA

66

88%

Geographical Distribution of Patients with ≥ 1 switches (n=115 vs. 75)

East Anatolia

6

5%

1

1%

South Eastern Anatolia

10

9%

9

12%

Marmara

39

34%

9

12%

Aegean

4

3%

4

5%

Mediterrane

19

17%

16

21%

Black sea

9

8%

1

1%

Central Anatolia

28

24%

35

47%

Discontinuation

N of Patients with Confirmed Discontinued

205

34%

80

87%

Time to confirmed discontinuation (days)

117

78

98

60

Time to any discontinuation or censoring (days)

276

124

132

104

N: Number; %: Percentage; IFX: Infliximab; SD: Standard Deviation; NA: Not available.

 

 

 

 

 

Figure Kaplan Meier (KM) curve for any Infliximab Use for the Switcher and Continuers Cohorts during the Baseline and Follow up Period.


Disclosure: L. A. Ellis, Janssen, 3,Johnson & Johnson, LLC, 1; I. Simsek, Janssen Scientific Affairs, LLC, 2; L. Xie, Janssen Scientific Affairs, LLC, 5; A. Ogbomo, Janssen Scientific Affairs, LLC, 5; D. Parenti, Janssen, 3,Johnson & Johnson, LLC, 1; K. Goyal, Janssen, 3,Johnson & Johnson, LLC, 1; Y. Yazici, Yusuf Yazici, 2.

To cite this abstract in AMA style:

Ellis LA, Simsek I, Xie L, Ogbomo A, Parenti D, Goyal K, Yazici Y. Analysis of Real-World Treatment Patterns in a Matched Sample of Rheumatology Patients with Continuous Infliximab Therapy or Switched to Biosimilar Infliximab [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/analysis-of-real-world-treatment-patterns-in-a-matched-sample-of-rheumatology-patients-with-continuous-infliximab-therapy-or-switched-to-biosimilar-infliximab/. Accessed .
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