Table 1 |
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Summary of clinical efficacy scores from trials evaluating abatacept |
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ACR20 (%) |
ACR50 (%) |
ACR70 (%) |
DAS28 LDAS (%) |
DAS28 remission (%) |
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Trial authors |
Study phase |
Study cohort |
n |
Duration |
Background therapy |
A |
P |
A |
P |
A |
P |
A |
P |
A |
P |
|
|
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Moreland et al. [19] |
II |
DMARD failure |
214 |
3 months |
None |
53% |
31% |
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Kremer et al. [20] |
II |
MTX failure |
339 |
6 months |
MTX |
60% |
35.3% |
36.5% |
11.8% |
16.5% |
1.7% |
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Kremer et al. [21] |
II |
MTX failure |
339 |
1 year |
MTX |
62.6% |
36.1% |
41.7% |
20.2% |
20.9% |
7.6% |
49.6% |
21.9% |
34.8% |
10.1% |
|
Kremer et al. [22] |
III (AIM) |
MTX failure |
652 |
1 year |
MTX |
73.1% |
39.7% |
48.3% |
18.2% |
28.8% |
6.1% |
42.5% |
9.9% |
23.8% |
1.9% |
|
Genovese et al. [29] |
III (ATTAIN) |
TNF-α antagonist Failure |
391 |
6 months |
MTX, other DMARD |
50.4% |
19.5% |
20.3% |
3.8% |
10.2% |
1.5% |
17.1% |
3.1% |
10% |
0.8% |
|
Schiff et al. [28] |
III (ATTEST) |
MTX failure: abatacept (A) or infliximab (I) active arms |
431 |
6 months |
MTX |
A: 66.7% |
41.8% |
A: 40.4% |
20% |
A: 20.5% |
9.1% |
A: 20.7% |
10.8% |
A: 11.3% |
2.9% |
|
I: 59.4% |
I: 37% |
I: 24.2% |
I: 25.6% |
I: 12.8% |
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1 year |
MTX |
A: 72.4% |
A: 45.5% |
A: 26.3% |
A: 35.3% |
A: 18.7% |
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I: 55.8% |
I: 36.4% |
I: 20.6% |
I: 22.4% |
I: 12.2% |
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For abatacept (A), only responses for 10 mg/kg are included. ACR20/50/70, at least 20%/50%/70% improvement in the American College of Rheumatology criteria for rheumatoid arthritis; AIM, Abatacept in Inadequate responders to Methotrexate; ATTAIN, Abatacept Trial in Treatment of Anti-TNF INadequate responders; ATTEST, Abatacept or infliximab versus placebo, a Trial for Tolerability, Efficacy and Safety in Treating RA; DAS28, Disease Activity Score using 28 joint counts; DMARD, disease-modifying antirheumatic drug; LDAS, low disease activity scores; LTE, long-term extension; MTX, methotrexate; P, placebo; TNF, tumor necrosis factor. |
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Buch et al. Arthritis Research & Therapy 2008 10(Suppl 1):S5 doi:10.1186/ar2416 |
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