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Study flow diagram
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Figure 1

Study flow diagram

Network diagram: ACR50 in people with rheumatoid arthritis who were MTX/other DMARD‐naive
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Figure 2

Network diagram: ACR50 in people with rheumatoid arthritis who were MTX/other DMARD‐naive

ACR50: biologic (with and without concomitant MTX) versus comparator
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Figure 3

ACR50: biologic (with and without concomitant MTX) versus comparator

HAQ: biologic (with and without concomitant MTX) versus comparator
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Figure 4

HAQ: biologic (with and without concomitant MTX) versus comparator

Remission: biologic (with and without concomitant MTX) versus comparator
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Figure 5

Remission: biologic (with and without concomitant MTX) versus comparator

Radiographic progression: biologic (+MTX) versus comparator
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Figure 6

Radiographic progression: biologic (+MTX) versus comparator

Withdrawals due to adverse events: biologic (with and without concomitant MTX) versus comparator
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Figure 7

Withdrawals due to adverse events: biologic (with and without concomitant MTX) versus comparator

Serious adverse events: biologic (with and without concomitant MTX) versus comparator
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Figure 8

Serious adverse events: biologic (with and without concomitant MTX) versus comparator

Cancer: biologic (with and without concomitant MTX) versus comparator
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Figure 9

Cancer: biologic (with and without concomitant MTX) versus comparator

Table 1. Characteristics of included studies

Study name

Biologic(s)

Biologic dose(s)

Number of study arms

Non‐biologic comparator

Concomitant use of MTX

Trial duration

RA duration

Biologic‐naive

Total number of participants

Bejarano 2008

Adalimumab

SD

2

MTX + PL

Yes

13 months

Established

Yes

148

Bejarano 2010

Infliximab

SD

2

MTX + PL

Yes

8 years

Established

No

20

Breedveld 2006

Adalimumab (+/‐ MTX)

SD

3

MTX + PL

Yes

24 months

Established

Yes

799

Detert 2013

Adalimumab

SD

2

MTX + PL

Yes

12 months

Early

Yes

172

Durez 2007

Infliximab

SD

2

MP + MTX

Yes

12 months

Early

No

29

Emery 2008 (COMET)

Etanercept

SD

2

MTX + PL

Yes

12 months

Established

Yes

542

Emery 2009 (GO‐BEFORE)

Golilumab (+/‐ MTX)

SD, HD

4

MTX + PL

Yes

12 months

Established

No

637

Kavanaugh 2013 (OPTIMA)

Adalimumab

SD

2

MTX + PL

Yes

6 months

Established

No

1032

Marcora 2006

Etanercept

SD

2

MTX

No

6 months

Unknown

Yes

26

Nam 2014a

Infliximab

SD

2

MP + MTX

Yes

6 months

Early

Yes

112

Nam 2014b

Etanercept

SD

2

MTX + PL

Yes

12 months

Early

Yes

110

Quinn 2005

Infliximab

SD

2

MTX + PL

Yes

12 months

Early

Yes

20

Rantalaiho 2014

Infliximab

SD

2

MTX + PL

Yes

24 months

Early

Yes

93

Soubrier 2009

Adalimumab

SD

2

MTX + PL

Yes

12 months

Established

No

65

St Clair 2004 (ASPIRE)

Infliximab

SD, HD

3

MTX + PL

Yes

12 months

Early

Yes

1049

Tak 2012

Rituximab

SD, LD

3

MTX + PL

Yes

24 months

Early

Yes

748

Takeuchi 2014

Adalimumab

SD

2

MTX + PL

Yes

6 months

Early

Yes

334

Tam 2012

Infliximab

SD

2

MTX

Yes

12 months

Established

Yes

40

Westhovens 2009

Abatacept

SD

2

MTX + PL

Yes

24 months

Established

No

509

HD: high dose; LD: low dose; MTX: methotrexate; PL: placebo; SD = standard dose

Figuras y tablas -
Table 1. Characteristics of included studies
Table 2. 'Summary of findings' table for biologics vs comparator in MTX/other DMARD‐naive people

Comparison

Direct evidence

Network meta‐analysis

Outcome: ACR50

No. of participants

(studies)

RR (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

RR (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

5720

(14 studies)

1.40 (1.30 to 1.49)

16% (13% to 20%)

NNTB = 7 (6 to 8)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)1

n/a

TNF biologic alone (without MTX)

versus comparator

850

(2 studies)

0.94 (0.73 to 1.22)

‐2% (‐11% to 7%)

NNTB = n/a

⊕⊕⊕⊖ moderate (downgraded for imprecision)2

1.00 (0.82 to 1.21)

0% (‐8% to 9%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

4463

(12 studies)

1.44 (1.34 to 1.54)

17% (13% to 21%)

NNTB = 6 (5 to 8)

⊕⊕⊕⊕ high3

1.42 (1.30 to 1.54)

18% (13% to 22%)

NNTB = 6 (5 to 8)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Non‐TNF biologic + MTX

versus comparator

1257

(2 studies)

1.27 (1.14 to 1.42)

13% (7% to 19%)

NNTB = 8 (6 to 14)

⊕⊕⊕⊕ high3

1.31 (1.11 to 1.52)

13% (5% to 22%)

NNTB = 8 (5 to 22)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Outcome: HAQ score

0‐3 (higher = worse): a measure of function

No. of participants

(studies)

Direct evidence

Network meta‐analysis

MD (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

MD (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

3872

(13 studies)

‐0.10 (‐0.16 to ‐0.04)

‐3.3% (‐5.3% to ‐1.3%)

NNTB = 4 (2 to 15)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)5

n/a

TNF biologic alone (without MTX)

versus comparator

557

(2 studies)

0.09 (‐0.24 to 0.41)

3% (‐8% to 13.7%)

NNTB = n/a

⊕⊕⊕⊖ moderate (downgraded for imprecision)2

0.17 (‐0.19 to 0.54)

5.7% (‐6.3% to 18%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

2615

(11 studies)

‐0.09 (‐0.26 to 0.07)

‐3% (‐8.7% to 2.3%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and inconsistency)2,6

‐0.08 (‐0.25 to 0.07)

‐2.7% (‐8.3% to 2.3%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Non‐TNF biologic + MTX

versus comparator

1257

(2 studies)

‐0.22 (‐0.26 to ‐0.18)

‐7.3% (‐8.7% to ‐6%)

NNTB = 2 (2 to 3)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)7

‐0.22 (‐0.55 to 0.11)

‐7.3% (‐18.3% to 3.7%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Outcome: Remission

(defined as DAS < 1.6 or DAS28 < 2.6)

No. of participants

(studies)

Direct evidence

Network meta‐analysis

RR (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

RR (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

5128

(15 studies)

1.62 (1.33 to 1.98)

15% (11% to 19%)

NNTB = 5 (6 to 7)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)8

n/a

TNF biologic alone (without MTX)

versus comparator

850

(2 studies)

1.08 (0.83 to 1.41)

2% (‐3% to 8%)

NNTB = n/a

⊕⊕⊕⊖ moderate (downgraded for imprecision)2

1.02 (0.74 to 1.39)

1% (‐7% to 11%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

4463

(12 studies)

1.55 (1.22 to 1.96)

14% (9% to 19%)

NNTB = 7 (5 to 10)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)9

1.62 (1.40 to 1.86)

18% (12% to 23%)

NNTB = 7 (5 to 10)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Non‐TNF biologic + MTX

versus comparator

1257

(2 studies)

2.10 (1.45 to 3.04)

19% (15% to 24%)

NNTB = 6 (4 to 9)

⊕⊕⊕⊖ moderate (downgraded for inconsistency)10

1.85 (1.46 to 2.28)

24% (13% to 35%)

NNTB = 6 (4 to 10)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Outcome: Radiographic progression

on Sharp/Van der Heijde modification (0‐448 points)

No. of participants

(studies)

Direct evidence

Network meta‐analysis

MD (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

MD (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

2256

(5 studies)

‐2.56 (‐6.03 to 0.92)

‐0.57% (‐1.35% to 0.21%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and inconsistency)2,11

n/a

TNF biologic + MTX

versus comparator

1747

(4 studies)

‐3.18 (‐6.80 to 0.43)

‐0.71% (‐1.52% to 959.82%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and inconsistency)2,12

‐3.73 (‐5.78 to ‐1.62)

‐0.83% (‐1.29% to ‐0.36%)

NNTB = 3 (3 to 7)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Non‐TNF biologic + MTX

versus comparator

509

(1 study)

‐0.43 (‐2.04 to 1.18)

‐0.22% (‐0.46% to 0.26%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and inconsistency)2,11

‐0.42 (‐4.22 to 3.41)

‐0.09% (‐0.94% to 0.76%)

NNTB = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Outcome: Withdrawals due to adverse events

No. of participants

(studies)

Direct evidence

Network meta‐analysis

RR (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

RR (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

5800

(14 studies)

1.32 (0.89 to 1.97)

2% (0% to 4%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for inconsistency and imprecision )1,2

n/a

TNF biologic alone (without MTX)

versus comparator

850

(2 studies)

1.14 (0.62 to 2.10)

0% (‐4% to 4%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.93 (0.41 to 1.90)

0% (‐2% to 3%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

4543

(12 studies)

1.60 (1.10 to 2.32)

3% (1% to 4%)

NNTH = 35 (17 to 183)

⊕⊕⊕⊖ moderate (downgraded for imprecision)14

1.68 (1.16 to 2.56)

3% (1% to 5%)

NNTH = 31 (14 to 138)

⊕⊕⊕⊖ moderate (downgraded for indirectness)4

Non‐TNF biologic + MTX

versus comparator

1257

(2 studies)

0.56 (0.31 to 1.01)

‐2% (‐5% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.56 (0.25 to 1.29)

‐2% (‐3% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Outcome: Serious adverse events

No. of participants

(studies)

Direct evidence

Network meta‐analysis

RR (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

RR (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

4850

(12 studies)

1.05 (0.87 to 1.26)

1% (‐1% to 3%)

NNTH = n/a

⊕⊕⊕⊖ moderate (downgraded for imprecision)2

n/a

TNF biologic alone (without MTX)

versus comparator

319

(1 study)

0.46 (0.16 to 1.29)

‐4% (‐8% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.52 (0.16 to 1.30)

‐5% (‐9% to 3%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

3593

(10 studies)

1.14 (0.92 to 1.42)

1% (‐1% to 3%)

NNTH = n/a

⊕⊕⊕⊖ moderate (downgraded for imprecision)2

1.16 (0.90 to 1.51)

2% (‐1% to 4%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Non‐TNF biologic + MTX

versus comparator

1257

(2 studies)

0.87 (0.64 to 1.18)

‐1% (‐5% to 2%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.87 (0.57 to 1.34)

‐1% (‐4% to 3%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Outcome: Cancer

(note: Peto OR used but can interpret as RR due to low event rate)

No. of participants

(studies)

Direct evidence

Network meta‐analysis

RR (95% CI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

RR (95% CrI)

Absolute risk difference, NNTB

Quality of evidence (GRADE)

Biologics + MTX

versus comparator

4611

(11 studies)

0.71 (0.38 to 1.33)

0% (0% to 0%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

n/a

TNF biologic alone (without MTX)

versus comparator

850

(2 studies)

0.79 (0.24 to 2.61)

0% (‐2% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.94 (0.25 to 3.18)

0% (‐1% to 2%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

TNF biologic + MTX

versus comparator

3863

(10 studies)

0.77 (0.35 to 1.69)

0% (0% to 0%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.81 (0.36 to 1.73)

0% (‐1% to 0%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Non‐TNF biologic + MTX

versus comparator

748

(1 study)

0.62 (0.22 to 1.77)

0% (‐3% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for serious imprecision)13

0.64 (0.20 to 2.12)

0% (‐1% to 1%)

NNTH = n/a

⊕⊕⊖⊖ low (downgraded for imprecision and indirectness)2,4

Comparator = MTX and/or DMARD

GRADE Working Group grades of evidence
High quality (⊕⊕⊕⊕): we are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality (⊕⊕⊕⊖): we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality (⊕⊕⊖⊖): our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect
Very low quality (⊕⊖⊖⊖): we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect

CI: confidence interval; CrI; credible interval; DAS: Disease Activity Score; DMARD: disease‐modifying anti‐rheumatic drug; MTX: methotrexate; n/a: not available; NNTB/NNTH: number needed to treat for an additional beneficial/harmful outcome; OR: odds ratio; RR: risk ratio; TNF: tumor necrosis factor

1Downgraded for inconsistency: I2= 51%.
2Downgraded for imprecision: 95% CI estimate includes both null effect and appreciable benefit or harm.
3No evidence of imprecision or inconsistency. Number of events > 300.
4Downgraded for indirectness/intransitivity due to differing participant characteristics (established vs late RA; types of failures); differing biologic doses and co‐interventions; and differing comparators.
5Downgraded for inconsistency: I2= 93%.
6Downgraded for inconsistency: I2= 90%.
7Downgraded for inconsistency: I2= 95%.
8Downgraded for inconsistency: I2= 75%.
9Downgraded for inconsistency: I2= 81%.
10Downgraded for inconsistency: I2= 65%.
11Downgraded for inconsistency: I2= 97%.
12Downgraded for inconsistency: I2= 96%.
13Downgraded twice for serious imprecision ‐ few events (< 300) and 95% CI estimate includes both null effect and appreciable benefit or harm.
14Downgraded for imprecision ‐ few events (< 300)

Figuras y tablas -
Table 2. 'Summary of findings' table for biologics vs comparator in MTX/other DMARD‐naive people