Declines of tender and swollen joint counts between 1985 and 2001 in patients. with rheumatoid arthritis seen in standard care:

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ARD Online First, published on December 8, 2005 as 10.1136/ard.2005.044131 1 2 3 1 Declines of tender and swollen joint counts between 1985 and 2001 in patients with rheumatoid arthritis seen in standard care: Possible considerations for revision of inclusion criteria for clinical trials 1 Theodore Pincus, M.D., 1,2 Tuulikki Sokka, M.D., Ph.D., 1 Cecilia P. Chung, M.D.,M.P.H., 3 Gail Cawkwell, M.D.,Ph.D. Division of Rheumatology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee Jyväskylä Central Hospital, Jyvaskyla, Finland Pfizer, Inc., New York, New York Address Correspondence to Theodore Pincus, M.D. Division of Rheumatology and Immunology Vanderbilt University School of Medicine 203 Oxford House, Box 5, Nashville, TN 37232-4500 e-mail: t.pincus@vanderbilt.edu Key words: rheumatoid arthritis, Core Data Set, Clinical trials, standard care, inclusion criteria Supported in part by grants from Pfizer, Pharmacia, the Jack C. Massey Foundation, and by NIH Grant HL 67964 Running title: Joint Count in 1985, 2000, and 2001 Submitted: July 2005, Resubmitted October 24, 2005 Copyright Article author (or their employer) 2005. Produced by BMJ Publishing Group Ltd (& EULAR) under licence.

ABSTRACT Objective: To analyze tender and swollen joint counts in 3 cohorts of patients with rheumatoid arthritis (RA) seen in standard clinical care in 1985, 2000 and 2001, to compute the proportions of patients who had fewer than 6-12 tender or swollen, as possible evidence-based information toward more generalizable inclusion criteria for current and future RA clinical trials. Methods: Tender and swollen joint counts were analyzed in 3 RA patient cohorts seen in Nashville, TN, USA: 125 seen in 1985, 152 in 2000, and 232 with early RA seen in a different setting in 2001. Results: The median number of tender was 11 in 1985, versus 2 in 2000 and 4 in 2001, while the median number of swollen was 12 in 1985, versus 6 in 2000 and 5 in 2001. The number of tender among 28 assessed was >12, >6, >4, and >3 in 47%, 80%, 85% and 90% of patients in 1985, versus 20%, 37%, 44% and 49% in 2000, and 17%, 37%, 50% and 58% in 2001. The number of swollen among 28 assessed was >12, >6, >4, and >3 in 51%, 78%, 85% and 90% of patients in 1985, versus 20%, 50%, 64% and 67% in 2000, and 14%, 46%, 58% and 72% in 2001. More patients had >6 tender in 1985 (80%) than >3 tender in 2000 (49%) and 2001 (58%), or >6 swollen in 1985 (78%) than >3 swollen in 2000 (67%) and 2001 (72%). Conclusion: Contemporary cohorts of patients seen in standard care have lower numbers of tender and swollen than in previous times. These findings might suggest consideration of revision of inclusion criteria for numbers of tender and swollen in contemporary RA clinical trials to improve generalizability. 2

INTRODUCTION The joint count is the most specific clinical measur to quantitate disease activity in patients with rheumatoid arthritis (RA). A tender and swollen joint count are included in the disease activity score (DAS) (1-3) and American College of Rheumatology (ACR) Core Data Set (4-6). Criteria for eligibility of patients to participate in RA clinical trials generally include 6-12 tender and 6-12 swollen (7;8). We reported that the majority of consecutive patients in two cohorts of patients with RA seen in standard clinical care in Nashville, TN, USA, in 2000 and 2001 did not have 6 swollen or tender (7;8). Furthermore, the 2000 cohort appeared to have substantially more favorable clinical status than a cohort of patients seen in the same setting in 1985, the majority of whom did have 6 or more tender and swollen (9). These observations suggested that 6-12 tender and swollen appeared to be appropriate inclusion criteria for RA clinical trials in past decades, but may be overly stringent at this time. Possible reduction in the number of tender and/or swollen required for inclusion might improve generalizability of contemporary and future RA clinical trials. However, relatively little published data are available concerning the specific number of tender or swollen, particularly fewer than 6, in patients outside of clinical trials, as formal joint counts are usually not performed by most rheumatologists in standard care (10). Therefore, in this report, we analyze the prevalence of 2-6 tender or swollen in patients in the 3 cohorts from standard care. 3

PATIENTS AND METHODS Patients Three patient cohorts were analyzed. All patients met American Rheumatism Association (ARA) criteria for RA (11) at some time. These studies were approved by the Vanderbilt Institutional Review Board for the protection of human subjects. The 1985 cohort included 210 patients who were identified at 3 sites, the weekly Vanderbilt University rheumatology clinic of TP, as well as the Nashville Veterans Administration Medical Center, and the private practice of Dr. Joseph Huston in Nashville. This cohort had been assembled in 1984-86 to provide baseline data for a longitudinal observational study to analyze whether a modified health assessment questionnaire (MHAQ) would predict premature mortality prospectively in patients with RA, as a patient questionnaire at baseline in 1973 had been found to be a significant predictor of survival over 9 years in 1984 retrospective analyses (12). The newer cohort to be observed prospectively would also have available quantitative joint count, radiographic scores and laboratory tests, which had not been available at baseline for the earlier cohort. In order to compare patients in the same rheumatology clinical setting 15 years apart, only the 125 consecutive patients seen at by TP Vanderbilt University are included in this report; the 85 patients seen at the 2 other sites are not included, particularly as data from the Veterans Administration Medical Center may have biased the results toward poorer status in 1985. The mean age of the 125 patients in the 1985 Cohort was 55 (range 30-87) years; 65% of the patients were female, 86% were Caucasian, and 86% were rheumatoid factor positive. The mean formal education level was 11 years, and mean duration of disease 9.6 years. Among all patients, 63% took a disease modifying antirheumatic drug (DMARD) including prednisone, 33% took any DMARD not including prednisone (30% took only prednisone) and only 10% took methotrexate. Further data concerning this cohort are found in previous reports (9;13-18). The 2000 RA cohort included 152 consecutive patients with RA who were seen between January 1998 and June 2001 by the same rheumatologist (TP) at the same weekly academic rheumatology clinic. These patients had been under care of this rheumatologist for a mean of 4.6 years (range 0-19 years) and had a mean duration of 12.5 years of disease. Twelve patients did not have a joint count recorded and another 2 were taking biologic agents; therefore, 138 patients are included in this report. The mean age of the 138 (of 152 patients) in the 2000 Cohort was 58 years; 72% of the patients were female, 94% were Caucasian, and 58% rheumatoid factor positive. The mean formal education level was 13 years, and mean duration of disease 12.6 years. These patients were treated more aggressively according to a philosophy of attempting to control inflammation as completely as possible in order to prevent longterm damage (19); 87% took DMARDs including prednisone and 67% took methotrexate. Further data concerning this cohort are found in previous reports (7-9). A 2001 RA cohort included 232 patients of 5 rheumatologists at Arthritis Specialists of Nashville seen between February and October 2001, with symptoms which began in 1998 or later. All were under care in Nashville, TN, USA, but none were under care of TP at Vanderbilt University. Potentially eligible patients were identified through review of medical records on the day before scheduled appointments and through the treating physicians who identified new patients. The study was described 4

by the treating physician to appropriate patients; more than 90% of patients who were asked agreed to enroll in an early rheumatoid arthritis treatment evaluation registry (ERATER), and completed written informed consent for current and future monitoring. The mean age of the 232 patients in the early 2001 early RA Cohort was 54 years; 77% were female, 90% were Caucasian, 74% were rheumatoid factor positive. The mean level of formal education was 13 years and the mean duration of disease at study visit was 1.8 years or 21 months. The mean duration of symptoms was 5.1 months before the diagnosis. At the study visit, 22 (9.5%) of patients had RA symptoms for less than 6 months, 45 (19.4%) had symptoms 6-12 months, 64 (27.6%) 1-2 years, and 101 (43.5%) more than 2 years. These patients were also treated aggressively; 99% took DMARDs including prednisone, and 91% took DMARDs not including prednisone, including 80% took methotrexate. Further data concerning this cohort are found in previous reports (7;8;20;21). Measures of clinical status All patients were evaluated according to what has become known as a standard protocol to evaluate rheumatoid arthritis (SPERA) (22). This protocol includes all measures in the ACR Core Data Set to assess clinical status in RA (5), and the disease activity score (DAS) (1-3). In this report, only the joint count data are analyzed. A 28 joint count includes 10 proximal interphalangeal (PIP) of the hands, 10 metacarpophalangeal (MCP), 2 wrists, 2 elbows, 2 shoulders and 2 knees (3;16). The 42 joint count includes these plus 2 hips and 2 ankles, and 10 metatarsophalangeal (MTP) (8). 5

Statistical Analyses All data were entered into a microcomputer using Access software, with data entry and data management programs developed specifically for the SPERA review. The data were transferred to Statistical Package for the Social Sciences (SPSS 11.0 Chicago, IL) for the personal computer and analyzed according to descriptive statistics. The numbers of patients according to 12, 6, 5, 4, 3, 2 and 1 tender or swollen were analyzed as cross tabulations. Probability plots were computed to depict the proportion of patients found at continuous levels. RESULTS Tender joint counts In the 1985 Cohort, on a 28 joint count (Figure 1), 79.9% of patients had 6 or more tender, compared to 37% of patients in the 2000 Cohort and 36.6% of the 2001 early RA Cohort. On a 42 joint count, 50.4% of the 2001 early RA patients had 6 or more tender (Figure 1). Three or more tender were seen in 89.5% of the 1985 Cohort, 48.6% of the 2000 Cohort, and 57.8% of the 2001 early RA Cohort on a 28 joint count, as well as 66.4% of the 2001 early RA Cohort on a 42 joint count (Figure 1). More patients in the 1985 cohort had 6 or more tender on a 28 joint count (79.9%) than had even >1 tender joint in the 2000 Cohort (66.7%), and a similar proportion (79.8%) had >1 tender joint in the 2001 early RA Cohort. Furthermore, almost as many patients had 2 tender on a 42 joint count in the 2001 early RA Cohort (77.2%) as had 6 or more tender on a 28 joint count in the 1985 Cohort (79.9%). 6

Swollen joint counts In the 1985 Cohort, on a 28 swollen joint count (Figure 2), 78.2% of patients had 6 or more swollen, compared to 50% of patients in the 2000 Cohort, and 46.1% of the 2001 early RA Cohort. On a 42 joint count, 63.4% of the 2001 early RA patients had 6 or more swollen (Figure 2). Three or more swollen were seen in 90.3% of the 1985 Cohort, 67.4% of the 2000 Cohort, and 72.0% of the 2001 early RA Cohort on a 28 joint count. Furthermore, 84.1% of the 2001 early RA Cohort had 3 or more swollen on a 42 joint count (Figure 2). More patients in the 1985 Cohort had 6 or more swollen on a 28 joint count (78.2%) than had >2 swollen in the 2000 Cohort (73.2%) or >3 swollen in the 2001 early RA Cohort (72%). Furthermore, about as many patients had >4 swollen in the 2001 early RA Cohort on a 42 joint count (76.8%) as had 6 or more swollen on a 28 joint count in 1985 (78.2%). Percentiles of tender and swollen Each of the 3 cohorts were analyzed as percentiles of tender and swollen joint counts (Table 1). The 50 th percentile for tender on a 28 joint count was 11 for the 1985 Cohort, 2 for the 2000 Cohort, and 4 for 2001 early RA Cohort; on a 42 joint count, the 50 th percentile was 6 for the 2001 early RA Cohort (Table 1). Seven tender were seen in the 30 th percentile in the 1985 Cohort, compared to the 70 th percentile in both the 2000 and 2001 early RA Cohorts on a 28 joint count. Similarly, the 50 th percentile for swollen was 12 in the 1985 Cohort, 6 in the 2000 Cohort, and 5 in the 2001 early RA Cohort, and 8 in the 2001 early RA Cohort on a 42 joint count (Table 1). The 30 th percentile value of 8 swollen in the 1985 Cohort was similar to the 70 th percentile with 9 swollen in the 2000 Cohort and 8 swollen in the 2001 early RA Cohort, and 50 th percentile values of 8 on a 42 joint count in the 2001 early RA Cohort (Table 1). The cumulative proportion of patients at various levels of tender and swollen are depicted as probability plots (Figure 3). The probability plots again illustrate that 78%-80% of patients had 6 tender or 6 swollen in 1985 compared to only 37%-50% in 2000 Cohort and 2001 early RA Cohort. DISCUSSION In theory, a clinical trial of a new agent in any disease might include all consecutive patients who meet criteria for the diagnosis under study. Pragmatically, that is not possible, in part because some patients may have too little disease activity to be appropriate candidates for evaluation of a new therapy. In population-based studies of people who meet criteria for RA, more than half do not have progressive disease (23-25). Some of these people may have reactive arthritis and other forms of self-limited inflammatory arthritis, rather than progressive RA. Therefore, it is reasonable to include only patients with a given level of severity of disease activity in order to recognize possible responses to therapy. The DAS (1-3) and Core Data Set (4-6) have provided important advances in rheumatology clinical research, leading to standardized primary outcomes in RA clinical trials over the last decade. However, inclusion criteria in trials have remained similar to those of 2 decades ago, although the status of patients in recent studies appears to have improved substantially compared to previous decades (9;26-31). Differences 7

between the 1985 versus the 2000 and 2001 early RA Cohorts may be explained in part by responses to aggressive therapy, as only 10% of patients were taking methotrexate in 1985 compared to 67-80% in 2000 and 2001 (9). Furthermore, biologic agents were available in 2000 and 2001, although the two patients in 2000 cohort who were taking biologic agents were excluded from then analyses and fewer than 5% of the 2001 patients in this study were taking these agents at the time of the study. However, a secular trend to milder disease may also be present (9;32). The percentiles presented in this report provide an approach to benchmarking of clinical status in cohorts of RA patients, applied by Lassere et al (33), Wiles et al (34), Wolfe and Choi (35), and Krishnan et al (36). In this study, the focus is the change in joint count data. The 42 joint count data are presented to document that results are similar to the 28 joint count, in large part as the 28 joint count includes the most likely to be abnormal in patients with RA (16). The 2001 cohort was included in part so that patients of rheumatologists other than TP could be analyzed. Several limitations are seen in these studies. First, the data presented are derived from only 2 clinical settings in one city, Nashville, TN, USA. However, data from an earlier Nashville Cohort concerning functional declines (12), work disability (12), socioeconomic status and RA status (37), and premature mortality (12;38) proved generalizable to other sites (39;40). Furthermore, data from the 1985 Cohort, which was recruited in the same setting as the 2000 Cohort, also have proved generalizable to other sites (39;40), including reports concerning radiographic damage (15), a 28 joint count (16), the absence of correlation between joint tenderness and pain compared to radiographic findings (14), laboratory associations of HLA-DR4 with radiographic changes but not with measures of function (13), reliability of physical measures of functional status (18), correlations of patient questionnaire scores for functional status with traditional measures (17), work disability (41), socio-economic status and RA status (42-44) and premature mortality (44). A second limitation is that other inclusion and exclusion criteria beyond the joint count may affect generalizability of clinical trials, such as exclusions for age, comorbidities, ESR or CRP, as well as safety considerations and administrative issues. As noted, the focus in this study is the change in joint count data. The 3 cohorts studied provide an unusual opportunity to analyze in depth patients with RA in two different eras, 1985 versus 2000 and 2001, as most standard rheumatology care is conducted without quantitative data outside of laboratory tests. It appears that common joint count inclusion criteria for RA clinical trials were met by a majority of patients in 1985 and were not met in 2000 and 2001. The results may suggest consideration of revision of common joint count inclusion criteria for contemporary RA clinical trials. Acknowledgements: The authors thank Drs. Joseph H. Huston III, David S, Knapp, M. Porter Meadors, Kevin J. Myers, and Paul W. Wheeler for generous cooperation and encouragement of their patients to participate in the 2001 early RA Cohort, Melissa Gibson and Christopher Swearingen for helpful technical assistance. "The Corresponding Author has the right to grant on behalf of all authors and does grant on behalf of all authors, an exclusive licence on a worldwide basis to the BMJ Publishing Group Ltd and its Licensees to permit this article (if accepted) to be 8

published in ARD editions and any other BMJPGL products to exploit all subsidiary rights, as set out in our licence (http://ard.bmjjournals.com/misc/ifora/licenceform.shtml)." 9

Table 1. Percentiles of tender joint and swollen joint counts in 3 cohorts of patients with rheumatoid arthritis: 28 joint count in a 1985 Cohort 125 patients seen in 1984-1986; 28 joint count in a 2000 Cohort - 138 patients seen in 1998-2001; 28 and 42 joint counts in a 2001 early RA Cohort 232 patients whose mean disease duration was 1.8 years. Tender Joint Count Swollen Joint Count Cohort: 1985 2000 2001 2001 1985 2000 2001 2001 Percentile 28 28 28 42 28 28 28 42 10 2 0 0 0 3 0 0 1 20 5 0 0 1 5 0 2 3 30 7 0 1 2 8 2 3 5 40 9 1 2 4 10 4 3 6 50 11 2 4 6 12 6 5 8 60 13 4 5 8 13 7 6 9 70 16 7 7 11 15 9 8 11 80 19 11 10 15 18 12 9 13 90 23 18 15 22 22 15 13 20 10

11 Figure 1. Percentages of patients with different numbers of tender in 3 cohorts of patients with rheumatoid arthritis: 28 joint count in a 1985 Cohort 125 patients seen in 1984-1986; 28 joint count in a 2000 Cohort - 138 patients seen in 1998-2001; 28 and 42 joint counts in a 2001 early RA Cohort 232 patients seen in 2001 whose mean disease duration was 1.8 years. Figure 2. Percentages of patients with different numbers of swollen in 3 cohorts of patients with rheumatoid arthritis: 28 joint count in a 1985 Cohort 125 patients seen in 1984-1986; 28 joint count in a 2000 Cohort - 138 patients seen in 1998-2001; 28 and 42 joint counts in a 2001 early RA Cohort 232 patients whose mean disease duration was 1.8 years. Figure 3. Probability plots illustrating the cumulative percent of patients in 3 cohorts of patients with rheumatoid arthritis, according to the number of swollen and number of tender on a 28 joint count in 1985, 2000 and 2001, and a 42 joint count in 2001.

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Figure 1 1985 Cohort: Tender Joints (0-28) 2001 Cohort E: Tender (0-28) 100% 80% 79.9% 84.7% 89.5% 94.3% 96.7% 100.0% 100% 80% 79.8% 100.0% 60% 40% 46.8% 60% 40% 36.6% 50.0% 57.8% 69.0% 20% 20% 17.2% 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 2000 Cohort L: Tender (0-28) 2001 Cohort E: Tender (0-42) 100% 100.0% 100% 100.0% 80% 80% 77.2% 86.3% 60% 40% 20% 19.6% 37.0% 43.5% 48.6% 58.7% 66.7% 60% 40% 20% 29.7% 50.4% 61.2% 66.4% 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 Ann Rheum Dis: first published as 10.1136/ard.2005.044131 on 8 December 2005. Downloaded from http://ard.bmj.com/ on 17 November 2018 by guest. Protected by copyright.

Figure 2. 1985 Cohort: Swollen Joints (0-28) 2001 Cohort E: Swollen (0-28) 100% 80% 60% 40% 50.8% 78.2% 86.3% 90.3% 95.1% 97.5% 100.0% 100% 80% 60% 40% 46.1% 58.2% 72.0% 81.1% 89.3% 100.0% 20% 20% 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 0% 14.2% >=12 >=6 >=4 >=3 >=2 >=1 >=0 2000 Cohort L: Swollen (0-28) 2001 Cohort E: Swollen (0-42) 100% 80% 60% 63.8% 67.4% 73.2% 79.0% 100.0% 100% 80% 60% 63.4% 76.8% 84.1% 100.0% 93.6% 89.7% 40% 50.0% 40% 20% 20.3% 20% 29.3% 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 0% >=12 >=6 >=4 >=3 >=2 >=1 >=0 Ann Rheum Dis: first published as 10.1136/ard.2005.044131 on 8 December 2005. Downloaded from http://ard.bmj.com/ on 17 November 2018 by guest. Protected by copyright.