Seven-year follow-up of infliximab therapy in rheumatoid arthritis patients with severe long-standing refractory disease: attrition rate and evolution of disease activity
© Vander Cruyssen et al.; licensee BioMed Central Ltd. 2010
Received: 26 November 2009
Accepted: 6 May 2010
Published: 6 May 2010
This study is based on the results from a Belgian expanded access program in which patients with active refractory and erosive rheumatoid arthritis (RA) were treated with intravenous infusions of infliximab in combination with methotrexate. The objectives of this study were to evaluate the continuation rate of infliximab and its clinical effect over a 7-year period and to document the reasons for discontinuation.
Between 2000 and 2001, 511 patients with severe and refractory RA were enrolled and treated with infliximab. After 7 years, apart from routine clinical follow-up, treating rheumatologists were asked to complete a questionnaire designed specifically for the present study to evaluate the current therapy with infliximab, the level of disease activity (Disease Activity Score in 28 joints [DAS28]) and the reasons for infliximab discontinuation.
After 7 years, 160 of 511 patients (31%) were still on infliximab treatment. The major reasons for infliximab discontinuation included lack of efficacy (104 patients), adverse events (107 patients) and elective change of therapy (70 patients). The majority of cases of treatment discontinuation for safety reasons occurred during the first 2 years. In contrast, discontinuation due to ineffectiveness showed a more constant rate over the 7-year period. Mean DAS for patients still on treatment with infliximab decreased from 5.7 (standard error [SE] 0.1) at baseline to 3.0 (SE 0.1) at year 4 and remained that low until year 7 (3.0 [SE 0.1]). Low disease activity (defined as DAS28 <3.2) was present in 60.9% of patients, and 45.5% achieved remission (DAS28 <2.6). DAS28 at the time of treatment discontinuation due to ineffectiveness decreased over the 7-year period from 5.6 (SE 0.3) in 2001 to 4.8 (SE 0.3) in 2008.
This observational study revealed that patients who continue to receive infliximab experience sustained clinical benefit. The majority of safety issues occurred during the first 2 years of infliximab therapy. We observed that the DAS at the time of therapy discontinuation showed a trend to decrease over time.
Anti-TNF agents have become standard treatment for patients with rheumatoid arthritis (RA) refractory to non-biologic disease-modifying anti-rheumatic drug (DMARD) therapy. Although there is strong evidence in support of the short-term efficacy and safety of these agents [1, 2], data from registries and cohorts are extremely important to evaluate the long-term treatment effects and safety issues.
Long-term treatment continuation rates reflect safety, efficacy and compliance with therapy. Infliximab, primarily used in combination with methotrexate (MTX), is a highly effective therapy for the majority of RA patients. After an induction scheme with intravenous infliximab infusions given at weeks 0, 2 and 6, infliximab is typically administered at a dose of 3 mg/kg every 8 weeks in combination with MTX. However, increasing the dose or shortening the dosing intervals is a common practice and may differ between countries according to social security regulations or guidelines and national recommendations .
Initiated between 2000 and 2001, the Belgian expanded access program (EAP) cohort is among the largest of that time, including 511 RA patients treated with infliximab therapy. The majority of these patients received infliximab at the standard regimen of 3 mg/kg in combination with MTX. Patients in the EAP could receive infliximab therapy (provided by Schering-Plough) before the product was reimbursed. We aimed to evaluate attrition of infliximab therapy in patients with long-standing refractory RA over a seven-year period and to document efficacy and the reasons for discontinuation, including safety issues.
Materials and methods
Five hundred and eleven RA patients entered the Belgian EAP between February 2000 and September 2001. These were the first Belgian patients to be treated with TNF blockade outside of a clinical trial setting. After European Medicines Agency approval of infliximab for the treatment of RA, patients could enter the EAP and receive infliximab, provided by Schering-Plough for free as part of a Medical Need Program (the Belgian EAP) until the product became reimbursable.
Patients were followed at different academic and non-academic centres. Clinical evaluations performed at each infliximab infusion included 28 and 66 of 68 swollen and tender joint counts, erythrocyte sedimentation rate (ESR; mm/hr), C-reactive protein (CRP) level (mg/L), Health Assessment Questionnaire (HAQ) , physician's global assessment of disease activity using a visual analogue scale (VAS; 0 to 100 mm) and patient's global assessment of disease activity (VAS 0 to 100 mm).
Baseline characteristics of the cohort
Disease duration (years)
Rheumatoid factor positivity (%)
Previous DMARDs (n)
Swollen joint count (n)
Tender joint count (n)
Serum CRP (mg/dL)
Patient's assessment of pain (VAS, 0--100 mm)
Patient's global assessment of disease activity (VAS, 0--100 mm)
Physician's global assessment of disease activity (VAS, 0--100 mm)
Health Assessment Questionnaire (score, 0--3)
After an induction regimen of 3 mg/kg at weeks 0, 2 and 6, all patients received maintenance therapy every 8 weeks. From six months onwards, the treating rheumatologist had the option of increasing the dose (typically by adding an extra vial of 100 mg infliximab) [7, 8]. The standard infliximab dosage of 3 mg/kg every eight weeks was reinstituted in the majority of patients between June and September 2002, when infliximab became a reimbursable medicine in Belgium at the standard dosage of 3 mg/kg every eight weeks. Due to this reimbursement issue, physicians had to reinstitute the standard dose of 3 mg/kg, but if needed, patients could continue receiving additional vials, provided for free by Schering-Plough.
During the first six months, steroid and MTX doses were kept stable; doses could be adjusted from six months onwards.
Ethically approved, written informed consent (Ghent University Hospital Ethical Committee 99/273) was obtained from all patients.
Statistical methods available in a classical statistical package (SPSS 17, Chicago, IL, USA) were employed in all analyses. These included calculation of means with standard error (SE) of means or medians for continuous variables and calculation of proportions for dichotomous variables. Kaplan-Meier curves were constructed after censoring of data at seven years. Continuation rates of infliximab therapy were calculated in the intent-to-treat format (taking into account all 511 patients initially enrolled in the study).
Continuation rates of infliximab therapy
Efficacy of infliximab therapy
Response on infliximab therapy
Percentage of patients obtaining low disease activity or remission at year 7 at the time of discontinuation
Mean DAS (SE)
Low disease activity
At year 7 (still on infliximab)
At discontinuation due to ineffectiveness
At discontinuation due to elective reason
At discontinuation due to safety issue
Concomitant medication at year seven
Ninety-four percent of patients still on infliximab at year seven received concomitant MTX at a median dosage of 12.5 mg/week, which was similar at baseline and in patients who dropped out. Forty-two percent of patients received concomitant corticosteroids at a median dosage of 5 mg/day.
The median dosage of infliximab given at year seven was 3 mg/kg every eight weeks. Overall, 33% of patients still on infliximab at year seven received a higher dose, mostly one additional vial.
Sixteen percent of patients still on infliximab at year seven received a dose increase between week 30 and September 2002. After the standard dose of 3 mg/kg was reinstituted from September 2002 onwards, 66% of those patients could remain on this standard dose; a dose increase (mostly by adding an extra vial) was needed in the remaining 33% of patients.
Of patients who did not receive a dose increase at week 30, 34% needed a dose increase at a later time.
Evolution of (non-)acceptable disease activity over time
Between the start of the study and seven years of follow up, 104 patients discontinued infliximab due to ineffectiveness. Figure 3 shows that discontinuation due to ineffectiveness follows a rather linear trend over time. The remaining disease activity not acceptable to the physician and leading to discontinuation of therapy showed a trend to decrease over time. Mean DAS28 at the time of treatment discontinuation due to ineffectiveness evolved over the seven-year period from 5.6 (SE 0.3) in 2001 to 4.8 (SE 0.3) in 2008.
Seventy patients electively discontinued therapy, meaning that the reason to discontinue infliximab was not directly related to the product. In cases in which the reason was specified, the majority of patients who discontinued infliximab due to elective reasons attributed the discontinuation to the wish (patient's or physician's) to switch to subcutaneous TNF blockers. Figure 5 shows that most patients discontinued infliximab due to elective reasons between year three and year four, when a new subcutaneous TNF blocker (adalimumab) became available in Belgium.
Also, patients who electively discontinued therapy previously experienced a good response to infliximab, which is reflected by the fact that 61.7% of patients had low disease activity and 46.7% of patients were in remission at the time of discontinuation.
Description of safety issues
Over seven years of follow up, 107 patients discontinued infliximab therapy due to safety issues.
Description of cases with (suspected) tuberculosis
Start date of infliximab
Date of symptoms
Peritoneal and pulmonary TB
Positive culture on BAL
Suspicion of tubercular pleuritis
Multiple negative cultures
Suspicion of military TB
Multiple negative cultures
Suspicion of GI TB adenitis
Granulomatous disease on pathology, but cultures negative
(4 March 2003)
Suspicion of TB pleuritis
Multiple negative cultures
PPD unk, chest x-ray nl
Twenty-five patients discontinued therapy due to infusion reactions. There were 19 malignancies: eight lymphomas, four breast cancers, two lung cancers, two ovarian cancers, one colorectal cancer, one thyroid cancer and one spinocellular cancer.
Additional safety issues included pericardial effusions (n = 4), nephritis (n = 2), disease-related complications (n = 2), polyneuropathy and demyelinating disease (n = 2), alopecia (n = 2), lung embolism (n = 1), coronary disease (n = 1), cardiomyopathy (n = 1) and other/non-specified safety issues (n = 7). Delay or skip of an infusion due to an infection or in the context of an operation was not considered as a 'stop due to safety issue'. Only patients who stopped and did not restart therapy were considered/available for this analysis.
Description of deaths
In addition to the previously described safety issues, 17 deaths occurred during infliximab therapy. Four patients died due to cardiac disease (three infarctions, one heart failure), one patient died due to an abdominal aneurysm, two patients died due to infections (pneumonia combined with perforating colitis, endocarditis), two patients died due to pulmonary embolisms, one patient died due to emphysema, one patient died due to demyelinating disease and two patients committed suicide. The reason for death was not available for four patients.
If patients stopped due to a safety issue, but died later on (more than two months later), this event was coded as a safety issue. This was the case for four patients: two patients with lung cancer and two patients with lymphoma.
Evolution of safety issues over time
Figure 4 shows the cumulative frequencies of discontinuation due to safety issues over time. From this curve, we found that the majority of safety issues leading to discontinuation of infliximab therapy occurred during the first two years.
Further analysis showed that 50% of infusion reactions occurred before week 104 and 50% of infections occurred before week 82.
This study describes the seven-year continuation rates, safety and efficacy of infliximab in a large cohort of patients with severe long-standing refractory RA. Of the initial 507 patients who started therapy, 49 patients were lost to follow up after seven years. This is less than 10% of patients, which is acceptable for interpreting the evaluation of continuation rates, safety and efficacy of therapy. Of the remaining 441 patients, 160 (36%) were still receiving infliximab therapy after seven years.
Due to the chronic nature of RA, requiring therapy for many years, long-term data to evaluate the efficacy and safety of the compounds are very important. This information can be obtained by cohorts or extensions of controlled trials, mostly focusing on one compound [10, 11], or by registries [12–14]. This study could possibly bridge the gap between extensions of clinical trials and nationwide registries: the inclusion criteria of the program were based on inclusion criteria similar to the daily clinical practice reimbursement criteria, and less stringent compared with clinical trials. Due to limited time span of inclusion, this study can be considered as an inception cohort, which has specific advantages for the analysis of trends over time, which is more difficult in registries.
Differences in baseline characteristics may be a reason for heterogeneity between studies. The heterogeneity between the different studies results in large differences in retention rates and Kaplan-Meier curves of anti-TNF therapy survival. The patients presented in this cohort suffered from severe long-standing disease, which may differ from that in patients in more recent studies and registries, in whom disease duration and activity tend to be less severe .
Interestingly, in this study, we were able to evaluate the different reasons for discontinuation over time. Discontinuation due to ineffectiveness seemed to be quite constant over time, resulting in a linear Kaplan-Meier curve (Figure 3), whereas discontinuation due to safety issues was most frequent during the first two years of therapy. This resulted in a decline of the slope of the curve over time (Figure 4). Finally, discontinuation due to elective reasons not directly related to product safety or ineffectiveness was most frequent around year four (Figure 5), when a new subcutaneous TNF blocker (adalimumab) became available in Belgium.
Regarding discontinuation, several factors should be taken into account. First, the acceptance of remaining disease activity may differ between physicians and patients and change over time. When patients have failed several therapies and few alternatives are available, one can assume that more remaining disease activity will be tolerated. In contrast, when more alternatives become available, one can assume that less remaining disease activity will be tolerated, resulting in an earlier start of a new biologic therapy  and earlier switching of therapies. In this study, mean DAS28 at the time of treatment discontinuation due to ineffectiveness showed a trend to decrease over time from 5.6 in 2001 to 4.8 in 2008. Second, discontinuation due to safety issues may differ between populations and eras. For example, a large proportion of patients in this cohort started infliximab therapy before general TB screening was recommended. With mandatory screening, it is possible that some TB cases in this cohort could have been avoided.
Finally, discontinuation due to elective reasons may be highly dependent on local situations (eg, reimbursement rules, national guidelines, access to infusion clinics) and the availability of new therapeutic options.
Long-term infliximab therapy seems to be efficacious and safe. More than 60% of patients still on infliximab at the seven-year follow up had low disease activity, and more than 45% of patients who continued infliximab treatment were in remission at year seven. Similarly low disease activity was observed in patients who discontinued therapy due to elective reasons. Higher levels of disease activity were observed at the time patients discontinued therapy due to safety issues or ineffectiveness.
Most safety issues resulting in therapy discontinuation occurred during the first two years of therapy. This was especially true for infusion reactions and infections. The trend toward a decrease in infection rates in the long term might be caused by the elimination of subgroups of patients determined to be at higher risk for infections on anti-TNF therapy. No unexpected cases of atypical infections were observed in this cohort.
Unfortunately, a majority of patients had to withdraw from infliximab therapy. Extrapolating the data from other registries and compounds (biologics and DMARDs) [16, 17] over 5 to 10 years demonstrated that, irrespective of the compound, more than half of RA patients will drop out of therapy. This suggests that further research is needed on the optimisation of treatment strategies in this era, when an increasing number of compounds became available for the treatment of patients with this chronic disease.
This study describes the seven-year follow up of a cohort of 511 RA patients with long-standing refractory disease who were treated with infliximab in combination with MTX.
After seven years, the majority of patients had to withdraw from infliximab therapy; one-third of patients who continued to receive infliximab experienced sustained clinical benefit: more than 60% of patients still treated with infliximab had low disease activity, and more than 45% were in remission.
Long-term treatment with infliximab appears to be safe: therapy discontinuation due to safety issues occurred mostly during the first two years of infliximab treatment.
Bert Vander Cruyssen is a post-doctoral researcher supported by the FWO Flanders.
Disease Activity Score in 28 joints
disease-modifying anti-rheumatic drug
expanded access program
erythrocyte sedimentation rate
Health Assessment Questionnaire
tumour necrosis factor
visual analogue scale.
The study was supported by a grant from Centocor, Inc. and Schering-Plough for the management of the database and the linguistic revision of the text
The authors thank Mr Joris Pieters, Denys Research Consultants, supported by Schering-Plough, for his assistance with the data collection.
A list of members for the Belgian Expanded Access Program (EAP) Rheumatoid Arthritis Study Group follows: Ackerman C, St-Lucas Ghent; Corluy L, Hasselt; Debrabanter G, St-Lucas Brugge; Declerck L, UZ Antwerpen; De Keyser F, Ghent University Hospital; Dhondt E, St-Jan Brugge; Durez P, Cliniques Universitaires Saint-Luc, Brussels; Herman L, Hamme; Hermans P, Ghent; Hoffman I, St-Augustinus Wilrijk; Janssens X, St-Lucas Ghent; Kruithof E, Elisabethziekenhuis Zottegem; Lensen F, H Serruysziekenhuis Oostende; Mielants H, Ghent University Hospital; Peretz A, CHU Brugmann, Brussels; Poriau S, AZ Alma Sijsele; Ravelingien I, OLV Aalst; Stuer A, H Hartkliniek Roeselaere; Vandenbruwaene F, H Hartkliniek Roeselaere; Vander Cruyssen B, Ghent University Hospital; Vanhoof J, Genk; Verbruggen L, AZ Vrije Universiteit Brussel; Volders P, Reumakliniek Genk; Westhovens R, University Hospitals K.U. Leuven
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