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Table 3 Information used to evaluate the proportion of patients achieving a response to a second biologic DMARD according to common criteria used in RA studies by reason for discontinuation of a first TNF-α inhibitora

From: Evaluating the efficacy of sequential biologic therapies for rheumatoid arthritis patients with an inadequate response to tumor necrosis factor-α inhibitors

Measure

Reason for discontinuation

Total number of patients

Estimated response rate, %

Biologics used to derive rate

Treatment duration range, months

Mean RA duration range, yr

Reference sources

ACR20

Intolerance

337

62.5

ADA and TNF2

3

12

[17, 36, 51, 53]

 

Lack of efficacy

251

48.4

ADA and ETN

3 to 4

9 to 12

[34, 36, 37, 53]

 

Loss of efficacy

609

58.0

ADA and ETN

3 to 6

9 to 12

[30, 34, 36, 37, 53]

ACR50

Intolerance

337

35.7

ADA and ETN

3

12

[17, 36, 51, 53]

 

Lack of efficacy

251

23.6

ADA and ETN

3 to 4

9 to 12

[34, 36, 37, 53]

 

Loss of efficacy

537

29.6

ADA and ETN

3 to 4

9 to 12

[34, 36, 37, 53]

ACR70

Intolerance

337

13.4

ADA and TNF2

3

12

[17, 36, 51, 53]

 

Lack of efficacy

251

9.0

ADA and ETN

3 to 4

9 to 12

[34, 36, 37, 53]

 

Loss of efficacy

537

12.0

ADA and ETN

3 to 4

9 to 12

[34, 36, 37, 53]

DAS28 <2.6

Intolerance

443

15.2

ABA and TNF2

3 to 6

NR

[17, 29]

DAS28 <3.2

Intolerance

211

30.4

TNF2

3 to 6

6

[17, 35]

 

Lack of efficacy

98

13.0

TNF2

3 to 6

6

[35]

 

Loss of efficacy

150

12.0

TNF2

3 to 6

6

[35]

EULAR moderate

Intolerance

250

38.8

TNF2

3 to 6

9

[38, 45, 50]

 

Lack of efficacy

98

37.0

TNF2

3 to 6

6

[35]

 

Loss of efficacy

150

18.0

TNF2

3 to 6

6

[35]

EULAR good

Intolerance

718

21.3

ADA and TNF2

3 to 12

6 to 12

[17, 35, 36, 38, 45, 50, 53]

 

Lack of efficacy

320

15.2

ADA, ETN and TNF2

3 to 6

6 to 12

[3537]

 

Loss of efficacy

515

16.9

ADA, ETN and TNF2

3 to 6

6 to 12

[3537]

EULAR moderate/good

Intolerance

467

69.5

ADA and TNF2

3 to 6

6 to 12

[17, 35, 36, 45, 53]

 

Lack of efficacy

349

63.2

ADA, ETN and TNF2

3 to 6

6 to 12

[3437, 53]

 

Loss of efficacy

687

60.7

ADA, ETN and TNF2

3 to 6

6 to 12

[3437, 53]

  1. aDMARD, disease-modifying antirheumatic drug; RA, rheumatoid arthritis; ACR, American College of Rheumatology; DAS28, Disease Activity Score 28 joint count; EULAR, European League Against Rheumatism; ABA, abatacept, ADA, adalimumab, ETN, etanercept, TNFi, ith TNF-α inhibitor; ABA, abatacept; ADA, adamlimumab; TNFi, ith TNF-α inhibitor. ACR20 means a 20% improvement in tender or swollen joint counts as well as 20% improvement in at least three of the following five criteria: patient assessment, physician assessment, erythrocyte sedimentation rate, pain scale and functional questionnaire. The ACR50 and ACR70 categories adhere to the same criteria, but for 50% and 70% improvement, respectively.