Article Text

Download PDFPDF

Responsiveness of the core set, response criteria, and utilities in early rheumatoid arthritis
  1. A C Verhoevena,
  2. M Boersb,
  3. S van der Lindena
  1. aDepartment of Rheumatology/Internal Medicine, University Hospital Maastricht, The Netherlands, bDepartment of Clinical Epidemiology, VU University Hospital, Amsterdam, The Netherlands
  1. Professor M Boers, Department of Clinical Epidemiology VE9–78, VU University Hospital, PO Box 7057, 1007 MB Amsterdam, The Netherlandsm.boers{at}


OBJECTIVE Validation of responsiveness and discriminative power of the World Health Organisation/International League of Associations for Rheumatology (WHO/ILAR) core set, the American College of Rheumatology (ACR), and European League for Rheumatology (EULAR) criteria for improvement/response, and other single and combined measures (indices) in a trial in patients with early rheumatoid arthritis (RA).

METHODS Ranking of measures by response (standardised response means and effect sizes) and between-group discrimination (unpaired ttest and χ2 values) at two time points in the COBRA study. This study included 155 patients with early RA randomly allocated to two treatment groups with distinct levels of expected response: combined treatment, high response; sulfasalazine treatment, moderate response.

RESULTS At week 16, standardised response means of core set measures ranged between 0.8 and 3.5 for combined treatment and between 0.4 and 1.2 for sulfasalazine treatment (95% confidence interval ±0.25). Performance of patient oriented measures (for example, pain, global assessment) was best when the questions were focused on the disease. The most responsive single measure was the patient's assessment of change in disease activity, at 3.5. Patient utility, a generic health status measure, was moderately (rating scale) to poorly (standard gamble) responsive. Response means of most indices (combined measures) exceeded 2.0, the simple count of core set measures improved by 20% was most responsive at 4.1. Discrimination performance yielded similar but not identical results: best discrimination between treatment groups was achieved by the EULAR response and ACR improvement criteria (at 20% and other percentage levels), the pooled index, and the disease activity score (DAS), but also by the Health Assessment Questionnaire (HAQ) and grip strength.

CONCLUSIONS Responsiveness and discrimination between levels of response are not identical concepts, and need separate study. The WHO/ILAR core set comprises responsive measures that discriminate well between different levels of response in early RA. However, the performance of patient oriented measures is highly dependent on their format. The excellent performance of indices such as the ACR improvement and EULAR response criteria confirms that they are the preferred primary end point in RA clinical trials.

  • rheumatoid arthritis
  • clinical trials
  • responsiveness

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Many end point measures are available to assess treatment efficacy in rheumatoid arthritis (RA). The OMERACT consensus on end point measures in RA facilitates comparison of results from different trials in treatment evaluation.1 The OMERACT initiative has called for further validation of the measures included in the World Health Organisation/International League of Associations for Rheumatology (WHO/ILAR) core set (also known as American College of Rheumatology (ACR) core set2) and combined measures (indices) such as improvement and response criteria.3 ,4To determine the applicability of a measure in a certain setting, the OMERACT filter has been proposed, containing three elements: truth, discrimination, and feasibility.5 The first two elements capture classic validity concepts. The topic of this study is discrimination. To be discriminative in trials, a measure has to detect clinically relevant change; moreover, it has to detect clinically relevant differences in change between treatment groups. Highly responsive measures are preferred because they allow clinical trials to be done with fewer patients, and also because they facilitate detection of small—but potentially important—differences in treatment effect.6 For the clinician, applying responsive measures in patient care will allow better tailoring of individual treatment. However, individual patient care may require another selection of measures than those used in trials: for example, assessment of morning stiffness and disease activity in the feet joints remains useful in the clinic despite their exclusion from the core set.7

As every measure is bound to pick up some noise together with the intended signal, its responsiveness is determined by the ratio of treatment effect to its variability (signal-to-noise ratio). Two classes of responsiveness statistics can be distinguished: the first is based on measurement of change in the course of a therapeutic intervention with known efficacy (external criterion, gold standard); the second is directed at the correlation of change in the tested measure with change in a “criterion measure”. However, as this last class of responsiveness statistics is based on the variability between subjects, regardless of whether group changes occur, they yield little information about the ability of a measure to detect treatment effects.8

The purpose of this study was to validate further the responsiveness of the core set, of the ACR improvement3 and European League for Rheumatology (EULAR) response criteria,4 and of other single measures and indices with data from a recent trial. The COBRA study9 (Dutch acronym: COmbinatietherapie Bij Reumatoïde Artritis) was a randomised controlled trial in patients with early RA that showed excellent clinical response, low toxicity, and less progression of radiographic joint damage with treatment of combined step-down prednisolone, methotrexate, and sulfasalazine, compared with treatment with sulfasalazine alone. The trial allowed us to create one “gold” and one “silver” standard for relevant response against which to validate performance of end point measures: we proposed the hypothesis a priori that patients in the combination group would on average show large and, certainly, relevant improvements at week 16 owing to the corticosteroid pulse (gold standard). Also, we assumed on the basis of the well known effects of sulfasalazine on disease activity that patients in the sulfasalazine-only group would also show relevant improvements, but to a lesser degree (silver standard).

We then ranked the end point measures and indices used in the COBRA study by their relative responsiveness, and also by their ability to discriminate between the (changes in the) treatment groups. Ultimately, this discriminatory ranking yields the most relevant results. However, one must realise that this ranking is post hoc: as the difference in response between the groups was the primary study question of the trial, the presence and extent of such a difference was unknown before the start of the trial.

Patients and methods


The COBRA study9 was a 56 week clinical trial that randomly assigned 155 patients with RA (ACR criteria10), aged 23–70, to one of two treatments. All patients had early, active disease (diagnosis <2 years). No prior treatment with disease modifying antirheumatic drugs, apart from antimalarial drugs, was allowed. One group was treated with a combination of sulfasalazine, methotrexate, and, initially, high dose oral prednisolone, the other group with sulfasalazine and double placebo. The prednisolone dose was 60 mg daily in the first week, tapered in weekly steps to the maintenance dose of 7.5 mg in week 7. Prednisolone and methotrexate (or the placebos) were tapered and stopped after weeks 28 and 40, respectively, while sulfasalazine was continued.


A broad variety of end points was assessed, including all disease activity measures of the WHO/ILAR core set.1 This comprises tender and swollen joint count (68 and 48 joints, respectively11), pain, assessor's and patient's global assessment (on a 10 cm visual analogue scales (VAS)), acute phase reactant (that is, erythrocyte sedimentation rate, Westergren method (ESR) or C reactive protein (CRP)), and physical function (by Health Assessment Questionnaire; Dutch HAQ12 ,13).


Non-core set measures included other joint counts and scores such as the Ritchie index, grip strength (by vigorimetry; Martin, Tottlingen, Germany, mean of medians of three measurements in both hands14), Arthritis Impact Measurement Scale (AIMS)15—a modified and validated Dutch version with scales for mobility, pain, and self efficacy, and the McMaster Toronto Arthritis patient preference questionnaire (MACTAR).16 The MACTAR is an instrument that follows improvement in five impaired activities, elicited and ranked in priority by the patient at baseline, together with changes in quality of life, psychological, social, and emotional wellbeing. Its scores increase as functional ability improves and vary from 11 (maximum deterioration) to 47 (maximum improvement). In its original format the baseline scores differ from the follow up scores because items inquiring about change are not included. To make these scores directly comparable mock change items were added at baseline and scored as “unchanged”. To compare the responsiveness and discriminatory power of different formats of patient global assessment (see ), two items from the MACTAR interview (change in disease activity by seven point Likert scale, and physical function by two questions with a six point scale), and a question on the actual state of disease activity (from a monitoring questionnaire; five point Likert scale) were evaluated together with the patient's global assessment of health indicated on a 10 cm VAS.


Whereas these disease-specific measures are sensitive to clinical change in RA, other—generic—measures yield a broader picture of patients' health status and allow comparison across a range of conditions.17 Utility served as the central concept of generic measures in the COBRA study.18 Utility is a single value or preference that patients assign to a particular health state. This value is expressed on a scale ranging from 1 (perfect health) to 0 (death) and takes into account both the positive effects of treatment and negative side effects. The rating scale and standard gamble methods assessed utility; the rating scale method derives utilities directly by asking the patients to place health states on a thermometer scale (that is, vertical VAS), the standard gamble method derives utilities from the patients' responses to decision situations under risk.19 ,20 Utility scores were assessed at baseline, and weeks 28 and 56.


Various indices (that is, composites from several measures) were assessed in the COBRA study (table 1). In fact, a pooled index of five measures (composite measure to reflect each patient's standardised improvement) was the assigned primary outcome. Pooling is a validated method to increase responsiveness of separate measures.21To obtain a patient's pooled index score, the standardised change score was calculated by dividing change in one measure by its pooled standard deviation of change for each treatment group at week 28. This procedure was repeated for five measures; the pooled index is the mean of standardised scores. Finally, a constant was added so that all index values started with a zero value at baseline. To obtain pooled index values for time points other than week 28, change scores at that point were divided by the same factor (the SD of change of the measure at week 28). The trial was designed before the conception of the WHO/ILAR core set.1 Recommendations at that time were to select five measures for maximum sensitivity to change22: tender joint count, global assessment by an independent assessor, ESR, grip strength, and MACTAR. The original disease activity score (DAS)23 was also calculated. This index contains the Ritchie tender joint index, swollen joint count, ESR, and patient's global assessment on a 10 cm VAS (calculation: 0.54(Ritchie) + 0.065(swollen joint count) + 0.33ln (ESR) + 0.072(patient's global).

Table 1

Definition of indices


Improvement in individual patients was also assessed in several ways: the ACR24 and DAS remission criteria,25ACR improvement3 and EULAR response4criteria, and count of improved core set measures26 (table1). Because fatigue was not measured in the trial “probable remission” described instances in which a patient would be in remission when absence of fatigue was assumed. Modified ACR improvement criteria and counts of improved core measures were also calculated with improvement thresholds varying from 0 to 70% (table 1). To calculate percentage improvement, values were recoded where necessary to ensure that all scales decreased on improvement.


Initially, grip strength, ESR, and patient's assessment of disease activity (five point Likert scale) were registered weekly by research nurses, later at least every four weeks. All other reported assessments—with the exception of utilities—were made at baseline and at weeks 16, 28, (40, and 56) by trained independent assessors who contacted the patients only at these times. In this way, the assessors were unaware of the effects of high dose prednisolone during the first six weeks of the protocol. Utility scores were assessed biannually; thus for these measures only 28 week follow up measures are reported.


All analyses were based on intention to treat: only five patients (3%, all in the sulfasalazine group) were lost to follow up before week 56 of the trial. The primary statistic of responsiveness was the standardised response mean (SRM): mean observed change from baseline divided by the standard deviation of this change.27 The effect size (ES)28: the mean change from baseline divided by the standard deviation (SD) of baseline scores was also calculated. Confidence intervals of SRMs were calculated with the assumption that its distribution is approximately Gaussian with mean zero and SD of one over the square root of the sample size.29 From the confidence intervals, statistical difference between SRMs could be evaluated. With no correction made for multiple comparison these findings are solely informative. Most evaluated variables are on an ordinal rather than interval or ratio scale level. However, as the underlying phenomenon (disease activity) is on an interval scale, these measures can be analysed parametrically if the sample size is large enough, as in the COBRA study database (central limit theorem).

Ceiling and floor effects may impair responsiveness when baseline values are found on the upper and lower end of the scale. We arbitrarily defined these extremes at the upper and lower one sixth of the scale (comparable with baseline HAQ scores <0.5 or >2.5) and analysed the variables in the core set.

As stated in the introduction, statistics based on change from therapeutic interventions need a priori confidence that the treatment is effective—that is, that the mean improvement in the treated group is relevant. The a priori criterion was a large change from baseline in the combined-treatment group at 16 weeks (“gold standard”); less change from baseline was expected in the group treated with sulfasalazine (“silver standard”). This proved to be true, though the change reached at 28 weeks was slightly larger, especially in the sulfasalazine-only group. Thus the combined-treatment group SRM at week 16 was the primary statistic of responsiveness to form a league table for responsiveness. The SRMs in the sulfasalazine group can be used to assess the ability of a measure to detect smaller—but still meaningful—changes, or changes occurring in a smaller proportion of the treatment group.

To indicate the discriminative power between groups unpaired Student'st test values are reported. χ2Values reflect between-group contrast (that is, discriminative power) in the nominal variables: improvement and remission criteria. Because the primary study question of the COBRA trial concerned contrast between treatment groups, this contrast could not be an a priori criterion such as improvement in the combined-treatment group as outlined above.30 Consequently, the ranking based on discrimination must be interpreted with caution. The 28 week data are included to allow further exploration of trends in responsiveness and discriminatory power.


The combined-treatment group included 76 and the sulfasalazine group 79 patients. The groups were balanced in important demographic and prognostic variables.9 ,18 At week 16 the mean improvement based on the pooled index was 1.4 for the combined-treatment group and 0.7 for the sulfasalazine group (p<0.0001). At week 28 these values were 1.5v 0.8 (p<0.0001). In the combined-treatment group rates and rapidity of ACR 20, 50, and 70 improvement were similar to those reported in recent trials on anti-tumour necrosis factor (anti-TNF) treatment (see below).

At week 16, most measures indicated large improvement from baseline in both groups (SRM 0.4–4.1, ES 0.3–3.2), and all measures except patient's global assessment of health (VAS) significantly distinguished between combined treatment and sulfasalazine (table 2, fig 1). Statistics of responsiveness were larger in the combined-treatment group than in the sulfasalazine group, confirming a priori assumptions of greater improvement in this group. The relative responsiveness ranking of measures was similar in both groups, suggesting the ranking is stable over a broad range of relevant response. However, in the sulfasalazine-only group the absolute differences in responsiveness between measures were less, in proportion to the overall decreased response. All indices (that is, pooled index, MACTAR, DAS, and count of improved core set measures) were—in both treatment groups—considerably more responsive than single core set measures such as tender joint count. The only exception to this was the highly responsive single item patient's assessment of change in disease activity on a seven point Likert scale. The responsiveness of most single measures was satisfactory but not equal (for example, high responsiveness for pain and ESR, lower for tender joint count and CRP). A confidence interval smaller than 0.5 around the SRM estimates indicates that a difference between SRMs of 0.35 or greater would be significant when tested at the two sided 0.05 level. The results at week 28 were generally similar (table 3, fig1).

Table 2

Indices of responsiveness at week 16 of follow up, for each treatment group, ordered by standardised response mean (SRM) of the combination group

Figure 1

Comparison of responsiveness and discrimination performance of end points. The order of the measures evaluated corresponds with that of table 3. Dark bars: standardised response means of the combination group at 16 (black) and 28 weeks (dark grey). Light bars: standardised response means of the sulfasalazine group at 16 (light grey) and 28 weeks (white). Dots: unpaired t values of the between-group comparison at 16 (black) and 28 weeks (white). pL = points Likert; MACTAR = McMaster Toronto Arthritis patient preference questionnaire; DAS = disease activity score; AIMS = Arthritis Impact Measurement Scale; HAQ = Health Assessment Questionnaire; VAS = visual analogue scale; ESR = erythrocyte sedimentation rate; RS = rating scale; CRP = C reactive protein; SG = standard gamble.

Table 3

Indices of responsiveness at week 28 of follow up, for each treatment group3-150

The format of patient assessment of disease activity, physical impairment, and global wellbeing strongly influenced responsiveness (for a description of the formats see ). The item in the MACTAR interview that asked for change of disease activity (seven point Likert scale) proved to be most responsive, patient's global assessment of health indicated on a VAS, least responsive. MACTAR, HAQ, some AIMS subscales, and single item patient global assessment of physical function were not equally responsive. The utility rating scale showed responsiveness close to the patient global assessment of disease activity, whereas utility measured by standard gamble was the least responsive of all measures.

Analyses on floor and ceiling effects showed that, of the core set variables, ESR and tender and swollen joint count were vulnerable to a certain degree of floor effect, with respectively 17, 15, and 15% of the patients in the lowest one sixth segment of the scale. Global and pain assessments, and also the HAQ had fewer patients that scored at the extremes of the scale.

The ranking for between-group discrimination showed interesting trends. This is best seen in fig 1: highest t values (that is, most discriminative power) were found for pooled index, count of core set measures improved by 50%, DAS, HAQ but, also, grip strength. Between the two assessments a catch-up effect is seen in the sulfasalazine group: whereas improvements in the combination group were already maximum at week 16, the sulfasalazine group improved further between week 16 and week 28, resulting in a smaller between-group difference (and thus a smaller t value).

At 16 weeks, ACR 20% improvement and EULAR response criteria showed large χ2 values, consistent with significant differences in response between treatment groups (table 4). The discriminatory performance of these criteria ranks high among all the measures tested (table 4): based on p values a χ2 value of 8 roughly corresponds with a t value of 3; similarly, a χ2 value of 12 corresponds with at value of 4, and a χ2 value of 25 with a t value of 5. At week 28 the differences between the groups were smaller. At week 16, modification of the percentage value in the ACR improvement criterion between 0% (no improvement, no worsening) and 50% did not change its discriminatory capacity; at week 28, this was also true for the 70% cut off point (table 4). The ACR and DAS remission criteria did not show a significant between-group difference.

Table 4

Discriminative ability of the preliminary ACR improvement criteria at different thresholds, EULAR response criterion, ACR and DAS remission criteria to distinguish between two treatment groups at two points of follow up


This study is the first independent confirmation of the responsiveness of the WHO/ILAR core set measures and response criteria in a trial of patients with early RA. In addition, it lends strong support to the use of other indices in such a trial. The conclusions are strong because they are based on the findings in two groups of patients with a high and moderate level of expected response. They extend the validity of both the core set and the ACRresponse criteria, because these had initially been selected, designed, and tested mainly in placebo controlled studies.

The fact that indices are more responsive than most single measures is not surprising, as combining measures (or items in a questionnaire) reduces scatter. Even a simple count of improved core set outcome variables proved to be a very responsive index, especially at the 20% threshold. Directly asking for change can also reduce scatter, even though the answer may be biased towards the current condition. Evidence for this is shown by the high responsiveness of the patient change question and the MACTAR (that incorporates many change items). The responsiveness of functional scales may be partly explained by the fact that they generally comprise several items in a multi-item questionnaire. Nevertheless, a set of two physical function questions on a six point Likert scale was also responsive.

The strong influence of format and content of the patient's global assessment questions on responsiveness is worrying. Similarly, the responsiveness of pain as a measure depends on the format. It is likely that the focus of doctors (or other assessors) is on the patients' disease, but this seems not always be the case for the patients themselves. Although not specified in great detail in the original formulation of the WHO/ILAR core set, we advocate focusing the format of patient oriented instruments on the disease, and paying close attention to the exact wording of the question(s).

Utility scores are advocated as a generic measure of treatment benefits. The two methods to derive utilities proved to have quite different levels of responsiveness. The rating scale (which is a patient preference rather than a true utility) performed adequately (comparable with observer's global assessment on VAS). However, the standard gamble method (a true utility because choices are made in a situation of uncertainty) showed low responsiveness. Economists prefer standard gamble because it conforms better to theoretical principles, but in practice its application was hindered by limited comprehension of the method by our patients and their risk aversive attitude. This phenomenon has been seen before in patient groups with a non-fatal or chronic disease.31 ,32

The data on between-group discrimination must be interpreted with caution. The extent of differences between the groups was not known before the trial, and might have been large in comparison with expected differences in current and future head-to-head trials. Nevertheless, the results are unique and extremely interesting as they indicate that responsiveness, the ability to detect change, may not parallel the ability to discriminate between different levels of response. Both the ACR improvement criteria (at various percentage levels) and the EULAR response criterion showed excellent discriminatory ability. This is at odds with the other trials in the review of Felsonet al, who concluded that 20% remained the best cut off point for the ACR criteria.33 A possible explanation is the relatively large contrast between treatment groups in the COBRA study.34 Other indices were also better discriminators than most single measures, with the exception of grip strength. In contrast, the discriminatory capacity of the MACTAR, though good, was less than expected based on its excellent responsiveness. This difference in performance between the HAQ and the MACTAR is hard to explain, and will need replication in other studies. Grip strength was included in the design of the trial based on the work of Anderson et al. 22 Despite its good performance in trials up to 1989, grip strength was eventually excluded in the core set for reasons of redundancy. Nevertheless, in early RA the fact that it is a composite measure of hand function with pain, swelling, stiffness, and muscle strength may contribute to its excellent performance. Muscle strength, particularly, may be a physical function variable with potency in early and established RA.35

From published reports we know that different responsiveness statistics—also those that are solely based on change from therapeutic intervention—may36 or may not37 yield different rank orders. In general, rankings based on paired Student'st test values and SRM will only be discrepant when different sample sizes are used for different measures. SRM is least influenced by sample size as it avoids the use of standard error of the mean in the denominator. Sample size was not an issue in this report as few values were missing. ES and SRM generally yield similar ranks, though discrepancies occur when the within-group SD at baseline (the denominator in the ES calculation) differs much from the SD of within-group change (the denominator in the SRM calculation). Obviously, ES cannot be calculated for measures that directly evaluate change, because they do not have a baseline variance. It may be a typical feature of these transitional measures—and indices that include change questions, such as the MACTAR—to pair a large SRM with a relatively small unpaired t value.

Despite their strong evidence, the data represent only one study in one subgroup—that is, early RA. The generalisability of our findings may be slightly limited, as the effects of treatment in the combined-treatment arm were large compared with many other trials in RA, but similar to those seen in recent anti-TNF trials. A meta-analysis of effectiveness of low dose corticosteroids in RA reported somewhat smaller ES in measurements of grip strength, swollen and joint tender count, and ESR (0.4–1.0) than we did; in particular, the ES values found in the corticosteroid treatment arms were smaller.38 However, the effect in the sulfasalazine group resembles that found in trials of methotrexate and intramuscular gold.39-42 Thus for studies of such moderately effective drugs, the ranking of the sulfasalazine group might be more appropriate.

Analyses on floor and ceiling effects showed that ESR and tender and swollen joint count were vulnerable to a certain degree of floor effect. The study's inclusion criteria towards disease duration and disease activity, with evaluation based on ESR and joint counts, probably prevented a serious floor effect in the study group. With global and pain assessments on a visual analogue scale, people tend to put their mark somewhere at the middle of the scale.

Buchbinder et al studied the ability of end points to discriminate between treatment effects in a placebo controlled trial of cyclosporin in RA.43 As the difference between cyclosporin and placebo was the primary study question of that trial, their approach is similar to the post hoc discrimination tests between treatment groups in this report. Compared with the COBRA study, differences between treatment groups were smaller for ESR and swollen joint counts but similar in other measures. They found doctor's and patient's global assessments (measured as a change question), as well as the AIMS pain subscale to be most discriminatory, and ESR and pain (five point scale) to be least discriminatory, with all other core set measures, including another doctor's global question, the HAQ, and a modification of the MACTAR (that is, PET), falling in between. These results agree with our observation on the importance of the exact format of the questions. The discrepancy found in the ESR is expected: lack of responsiveness of ESR is well known during treatment with cyclosporin. More surprising is the relatively poor performance of the physical function questionnaires. It may be that the cyclosporin trial included patients with longstanding disease and more fixed disability that was less likely to respond to treatment. Patients in the COBRA study had a median disease duration of only four months.

Differences in responsiveness, and especially discrimination, have important implications for trial design. The use of responsive and discriminative measures allows reduced patient numbers or detection of smaller—yet relevant—differences between groups. This is important especially in trials of early RA. Simpler trial design through use of a limited number of measures saves costs and effort, and facilitates interpretation of the results. In routine patient care, use of a limited number of highly responsive measures facilitates the collection and interpretation of long term follow up data. Obviously, additional measures should be applied according to the characteristics of the individual patient.

In summary, this study convincingly shows that responsiveness and the ability to discriminate between different levels of response are not identical concepts. The data provide strong evidence for the responsiveness and discriminatory capacity of the WHO/ILAR core set as well as the ACR and EULAR response criteria in the study of moderately and strongly effective drugs in early RA. However, where information is elicited from the patient, researchers should select and focus their instruments on the disease, as performance is strongly dependent on the exact format of questions.


AC Verhoeven is research-fellow in the COBRA trial supported by grant of the “Ziekenfondsraad, fonds Ontwikkelingsgeneeskunde” (92–045), The Netherlands.

Formats of items with patient assessment