Abstract
Clinical response in patients with rheumatoid arthritis (RA) treated with biologic agents can be influenced by their pharmacokinetics and immunogenicity. The present study evaluated the concordance between serum drug and antidrug levels as well as the clinical response in RA patients treated with biological agents who experience their first disease exacerbation while being on a stable biologic treatment. 154 RA patients treated with rituximab (RTX), infliximab (IFX), adalimumab (ADL), or etanercept (ETN) were included. DAS28, SDAI, and EULAR response were assessed at baseline and reevaluated at precise time intervals. At the time of their first sign of inadequate response, patients were tested for both serum drug level and antidrug antibodies level. At the next reevaluation, patients retreated with RTX that had detectable drug level had a better EULAR response (P = 0.038) with lower DAS28 and SDAI scores (P = 0.01 and P = 0.03). The same tendency was observed in patients treated with IFX and ETN regarding EULAR response (P = 0.002 and P = 0.023), DAS28 score (P = 0.002 and P = 0.003), and SDAI score (P = 0.001 and P = 0.026). Detectable biologic drug levels correlated with a better clinical response in patients experiencing their first RA inadequate response while being on a stable biologic treatment with RTX, IFX, and ETN.
1. Introduction
Rheumatoid arthritis (RA) is a chronic inflammatory disease that can result in substantial morbidity [1–3], impaired physical activity, and poor quality of life [4, 5], leading to a reduced life expectancy by 3 to 18 years [6] and increased mortality [7–11].
The targets of biologic agents are interactions between the immune cells (mainly T lymphocytes, B lymphocytes, and macrophages), which are responsible for inflammation and structural damage in affected joints, and the signaling molecules involved in their activation. The most used approved biologic agents for the treatment of RA are tumor necrosis factor (TNF) antagonists (infliximab, adalimumab, etanercept, golimumab, and certolizumab) or products that target B cells like rituximab (a chimeric monoclonal antibody that targets CD20 B cells) or inhibitor of costimulation of T cells (abatacept). Most of these agents are very effective at improving the signs and symptoms and at slowing or preventing structural damage in patients with RA [12–21]. Since the introduction of biologic treatment, prognosis of the disease has been substantially improved [22, 23].
Nevertheless, despite all these therapeutic advances and their relatively expensive costs, a variable proportion of patients with several autoimmune diseases including RA and inflammatory bowel diseases (IBD), who initially benefited from biologics, eventually lost response [24–26]. For example, a study from the Swedish TNF-antagonist registry found that 44% of patients were still taking their initial therapy at five years, and 25% were no longer taking any TNF antagonist at all [25]. As for IBD, up to 50% of patients lose response to treatment (secondary nonresponders) and up to 30% do not respond at all (primary nonresponders) [27]. The rational for lack or loss of response is multifactorial: molecular structure of biologic drug, pharmacokinetics, pharmacodynamics, and development of anti-drug antibodies.
In IBD, there are several strategies to the management of secondary failure to TNF antagonists [26]. These include switching to another drug in the same or different class, increasing the dose of biologic drug, changing concomitant immunosuppressive drug, or measuring drug levels and antibodies [28–30]. Therapeutic drug monitoring seems to be the adequate approach for the biologic treatment management [28]. Testing for drug levels and antibodies in secondary nonresponders is more cost-effective when compared to empiric drug escalation [31, 32]. It identifies those patients who will benefit from dose escalation versus those who are unlikely to respond to this strategy (high titers of anti-drug antibodies) [33].
Drug immunogenicity is one of the main mechanisms behind therapeutic failure also for RA patients [34–38]. Systemic reviews and meta-analysis conclude that anti-drug antibodies are clinically relevant and lead to significant decrease of therapeutic response [39]. Dose escalation in these patients may boost anti-drug antibodies production with serious adverse events [37, 40–42]. As for nonresponders without anti-drug antibodies but with detectable serum drug levels, these may respond better when switched to a drug with different mechanisms of action [43].
2. Methods
During a period of 2 years (January 2012–January 2014), we followed up 154 patients with established RA receiving one of the following biologic agents: rituximab (62 patients), infliximab (32 patients), etanercept (45 patients), and adalimumab (15 patients) with concomitant conventional synthetic disease-modifying antirheumatic drug (csDMARD) and few cases of monotherapy. Patients were included in order of their admission to the Department of Rheumatology, “Sfanta Maria” Hospital, Bucharest, Romania. All patients were previously diagnosed with RA according to ACR 1987 criteria [44] or ACR/EULAR 2010 criteria [45] and were treated using “treat to target” strategy [46] and local guidelines for the management of active RA [47]. The study was approved by the hospital Ethics Committee and all patients gave written informed consent before the study was started.
Demographic data, clinical (number of tender and swollen joints) and laboratory (ESR-erythrocyte sedimentation rate, CRP: C reactive protein, RF: rheumatoid factor, ACPA: anticyclic citrullinated peptide, IgG type) variables were collected at baseline and at each reevaluation. RA activity was evaluated in all patients by using 3 variables: Disease activity scores (DAS28 4v), Simplified Disease Activity Index (SDAI), and European League Against Rheumatism (EULAR) response. All clinical evaluations were performed by two independent assessors. As it was proposed at OMERACT 9 (Outcomes in Rheumatology) meeting [48], a RA flare represents a cluster of symptoms of sufficient duration intensity to require (re)initiation, change, or increase in therapy. Nevertheless, as suggested by several reports [49], in clinical research these criteria may be difficult to apply. Since there is no definition validated, we considered the situation as RA flare when at least one of the following conditions occurred: an increase in SDAI, an increase in ESR and/or CRP not due to a concomitant infection, an increase in DAS score to moderate or high disease activity, and a lower class in EULAR response as compared to previous reevaluation. At the moment of RA flare as described before, just before a new administration, patients were tested for anti-drug antibodies and biologic drug serum levels. According to serum drug levels patients were classified in group A if their serum drug levels were detectable and in group B if their drug levels were undetectable.
Patients were excluded from testing if their RA flare was related to conventional synthetic or biologic DMARD discontinuation, or a concomitant infectious disease, also if between baseline (the moment of serum drug level testing) and next reevaluation; patients had a change in their treatment regimen (increase in glucocorticoid dose and csDMARD dose or addition of a new immunosuppressive drugs). These particular patients were excluded from the final analysis. The reevaluation and clinical responses were assessed for each biologic drug: after 6 months from drug level testing, for RTX; after 2 months, just before a new i.v. infusion, for IFX; and after 3 to 4 months, for ETN and ADL.
2.1. Detection of Serum Drug Level and Anti-Drug Antibodies
Serum drug and antidrug levels were measured by enzyme linked immunosorbent assay (ELISA), using Progenika kits (Promonitor-RTX, Promonitor-anti-RTX, Promonitor-IFX, Promonitor-anti-IFX, Promonitor-ETN, Promonitor-anti-ETN, Promonitor-ADL, and Promonitor-anti-ADL). Several assays and technologies have been approved for monitoring serum drug and antidrug level [50], but bridging ELISA seems to be the only method with the potential for routine adoption in a hospital clinical setting for patient monitoring [37, 43, 51, 52]. It has been demonstrated that antibodies against TNF antagonists are anti-idiotypic, therefore neutralizing by definition [53]. Other technologies like cell-based assays, biacore, and homogeneous mobility shift assays can characterize the functionality of anti-drug antibodies; however, the question arises whether characterization of the antibody binding activity is required, when this can be easily answered with a simple ELISA test due to the fact that the immune response detected by ELISA is neutralizing. ELISA assays detect binding antibodies regardless of their functional activity. This method is similar for any other solid-phase methods like radioimmunoassays (RIA).
The clinical relevance of the immune response detected by ELISA is very well established and demonstrated in several studies [37, 51, 54, 55]. Promonitor kits have high accuracy for quantifying serum drug level, a pivotal importance to develop therapeutic algorithms [56].
In regards to drug levels detected by Promonitor kits, these span all clinically relevant drug concentrations (35–14400 ng/mL, 24–12000 ng/mL, 35–40000 ng/mL, and 665–240000 ng/mL for IFX, ADL, ETN, and RTX levels, resp.). ELISA tests used in this work have demonstrated an excellent correlation with other commercially available assays used for drug monitoring [56].
Cut-points of the anti-drug antibody tests are determined to be 2 AU/mL, 3.5 AU/mL, 142 AU/mL, and 340 AU/mL for anti-IFX, anti-ADL, anti-ETN, and anti-RTX antibodies, respectively. No human anti-drug antibody is currently available for anti-drug antibody screening; therefore outputs are given in arbitrary units per milliliter.
2.2. Statistical Analysis
Statistical analysis was performed using SPSS statistical software, version 20.0. The data were expressed as the mean ± SD. All statistical tests were two-sided and were performed at an α level of 0.05. The differences between groups were analyzed by Student's t-test, Kruskal-Wallis test, or Mann-Whitney test, as appropriate. Spearman's test was used for correlations.
3. Results
3.1. Characteristics of the Cohort
The study included 154 patients with established RA. One hundred and ten of them had a clinical or laboratory condition suggesting a disease flare during the evaluated period. Since final analysis, 38 patients met the exclusion criteria (8 patients had a significant increase in their glucocorticoid dose, 12 patients had csDMARD dose increase, 7 patients had a new csDMARD added to their treatment regimen, and 11 patients were switched to another biologic drug).
The final cohort of tested patients had the following treatment characteristics: 34.72% RTX patients (25 patients), 27.77% IFX patients (20 patients), 25% ETN patients (18 patients), and 12.5% ADL patients (9 patients). Their mean current biologic agent treatment was 41.79 ± 27.76 months in patients with RTX treatment, 34.45 ± 27.76 months with IFX, 49.38 ± 38.03 months with ETN, and 45.56 ± 23.88 months with ADL. The results showed that no detectable anti-drug antibodies were found in patients receiving RTX, ADL, and ETN. Patient's baseline characteristics are listed in Table 1.
Table 1.
Biologic agent | Current biologic treatment, duration, and mean | DAS28 baseline, mean | SDAI baseline, mean | csDMARD associated, no (%) | ACPA positive, no (%) | RF positive, no (%) |
---|---|---|---|---|---|---|
RTX | ||||||
Group A | 48.8 ± 53.4 | 3.65 ± 1.12 | 20.0 ± 15.7 | 15 (60%) | 14 (56%) | 16 (64%) |
Group B | 27.7 ± 13.7 | 3.45 ± 1.19 | 21.7 ± 29.6 | 8 (32%) | 4 (16%) | 7 (28%) |
P | 0.294 | 0.678 | 0.845 | 0.667 | 0.021 | 0.049 |
IFX | ||||||
Group A | 40.6 ± 39.9 | 3.57 ± 1.25 | 15.2 ± 19.7 | 6 (30%) | 4 (20%) | 7 (35%) |
Group B | 29.3 ± 17.5 | 5.42 ± 1.19 | 43.2 ± 29.6 | 6 (30%) | 3 (15%) | 4 (20%) |
P | 0.379 | 0.003 | 0.026 | 0.582 | 0.515 | 0.064 |
ETN | ||||||
Group A | 47.8 ± 38.5 | 4.14 ± 1.44 | 31.6 ± 31.3 | 10 (55.55%) | 11 (61.11%) | 12 (66.67%) |
Group B | 57.6 ± 23.7 | 5.25 ± 1.79 | 41.5 ± 40.3 | 3 (16.67%) | 2 (11.11%) | 2 (11.11%) |
P | 0.679 | 0.259 | 0.639 | 0.239 | 0.814 | 0.612 |
ADL | ||||||
Group A | 46.7 ± 25.2 | 3.39 ± 1.04 | 10.1 ± 6.05 | 7 (77.78%) | 4 (44.44%) | 6 (66.67%) |
Group B | 36 | 3.54 | 32.9 | 1 (11.11%) | 1 (11.11%) | 1 (11.11%) |
P | 0.700 | 0.902 | 0.009 | 0.708 | 0.495 | 0.571 |
Differences between patient's baseline characteristics were tested by Student's t-test or chi-square test.
RTX: rituximab; IFX: infliximab; ETN: etanercept; ADL: adalimumab.
Group A: detectable drug level; Group B: undetectable drug level.
csDMARD: conventional synthetic disease modifying antirheumatic drug; ACPA: anticitrullinated peptides antibodies status; RF: rheumatoid factor status.
At the moment of disease flare, 36% patients from the RTX group had undetectable drug level with 66.66% of them having moderate and high disease activity, mean DAS28 score of 3.45 ± 1.20. SDAI was lower in patients with detectable drug levels compared to patients with undetectable drug levels, 20.0 ± 15.7 versus 21.7 ± 29.6. There was no significant difference between groups A and B regarding both DAS28 score and SDAI (P = 0.678 and P = 0.845) nor treatment duration (27.75 ± 13.71 versus 48.81 ± 53.94, P = 0.294).
We found a significant difference in RTX serum level depending on ACPA status (P = 0.021). ACPA presence was positively associated with detectable RTX levels (OR = 8.75; 95%CI 1.21–63.4; P = 0.032) being a moderate predictor with AUC = 0.715; 95%CI: 0.5239–0.9067. This new finding supports the idea that patients positive for ACPA achieve a better clinical result being on treatment with B-cell depletion therapy. The mechanism by which these patients have higher RTX serum drug level should be studied further.
Interestingly, RTX serum level also correlated with the increased number of previous biologic agents (P = 0.009, r = 0.514). Sixty-two percent of patients with detectable serum RTX level had 2 anti-TNF agents as previous biologic treatment. Mention should be made that according to local guidelines, RTX is a second line biologic drug.
In the IFX treated patients, 90.90% (10 patients) of those with undetectable IFX serum level had moderate and high disease activity. Seven (63.63%) of these patients had anti-IFX antibodies. Surprisingly, anti-IFX antibodies were also found in 2 patients with subtherapeutic drug level. Twelve patients (60%) had a csDMARD associated: 8 patients had methotrexate, one patient had azathioprine, two patients had leflunomide, and one patient had sulfasalazine. Six patients did not have a csDMARD associated. Methotrexate dose range was between 7.5 mg and 20 mg/week. Our results showed that methotrexate association and the presence of anti-IFX antibodies were negatively correlated (P = 0.048, r = −0.447), confirming that methotrexate reduces IFX immunogenicity.
No anti-ETN antibodies were found in the 18 patients treated with ETN. At baseline, 77.77% of them had moderate and high disease activity evaluated by using DAS28 score and only 3 patients had undetectable drug levels. Also in this subgroup, there were 5 (27.7%) patients without a csDMARD, but all of them had detectable drug levels. Seven patients had methotrexate associated ranging from 10 mg to 20 mg/week and 6 patients had leflunomide 20 mg/day.
The group of patients treated with ADL that had a RA flare and were tested for drug levels was relatively small; 9 patients out of 15 patients enrolled in the study. Their mean DAS28 score was of 3.41. Moderate disease activity was found in 55.55% of them. No anti-ADL antibodies were detected. Only one patient had no csDMARD associated. Seven patients had methotrexate associated (10–20 mg/week, mean dose 15 mg/week) and one patient had leflunomide 20 mg/day.
3.2. Therapeutic Responses at Next Reevaluation after RA Exacerbation
During the follow-up period, patients from the final analysis remained on the same therapeutic treatment regimen regarding conventional synthetic and biologic DMARDs. Their EULAR responses are listed in Table 2.
Table 2.
EULAR response | ||||
---|---|---|---|---|
No | Moderate | Good | P | |
RTX | ||||
Group A | 4 (16%) | 5 (20%) | 7 (28%) | 0.038 |
Group B | 6 (24%) | 2 (10%) | 1 (4%) | |
IFX | ||||
Group A | 2 (10%) | 5 (25%) | 2 (10%) | 0.002 |
Group B | 10 (50%) | 1 (5%) | 0 | |
ETN | ||||
Group A | 3 (16.67%) | 5 (27.78%) | 7 (38.89%) | 0.023 |
Group B | 3 (16.67%) | 0 | 0 | |
ADL | ||||
Group A | 2 (22.22%) | 1 (11.11%) | 5 (55.56%) | 0.194 |
Group B | 1 (11.11%) | 0 | 0 |
Differences between EULAR responses in group A and group B were tested using Kruskal-Wallis test, for each biologic agent.
RTX: rituximab; IFX: infliximab; ETN: etanercept; ADL: adalimumab.
Group A: detectable drug level; Group B: undetectable drug level.
Six months after testing the serum drug levels, RTX treated patients that had detectable drug levels at baseline (group A) and had a mean DAS28 2.93 ± 1.20 compared to 3.27 ± 1.47 in group B (P = 0.01). Twenty-two percent of patients from group B still had high disease activity according to DAS28 score and only 3 patients in this group obtained remission. The differences in disease activity (remission, low, moderate, and high) using DAS28 score were significant between groups A and B (P = 0.003). There was also a significant difference in their SDAI evolution: mean SDAI in group A was 12.23 ± 14.13 and in group B was 14.83 ± 20.51 (P = 0.033).
Regarding EULAR response (no, moderate, and good) in RTX treated patients there was a significant difference in the evolution of the two groups (P = 0.038). Twelve patients from group A achieved good and moderate response compared to only 3 patients from group B (Table 2).
All patients treated with IFX were reevaluated after 2 months. The difference in DAS28 evolution between group A and group B was significant: 3.67 ± 1.24 versus 5.59 ± 1.07 (P = 0.002). None of the patients having undetectable drug level at first RA flare achieved remission or low disease activity. Clinical response was also significantly different regarding also SDAI evolution (group A mean SDAI 17.26 ± 12.29 compared to group B mean SDAI 44.33 ± 18.22, P = 0.001). EULAR response was better in patients having detectable drug level at flare (P = 0.002) (Table 2).
Anti-drug antibodies were detected in 45% of IFX treated patients: seven patients (35%) had undetectable IFX level and 2 patients (10%) had subtherapeutic IFX level. All patients having anti-IFX antibodies had no EULAR response at follow-up and appropriate therapeutic management was initiated. Patient's characteristics are listed under positive and negative anti-IFX antibodies (Table 3).
Table 3.
Positive anti-IFX antibodies | Negative anti-IFX antibodies | P value | |
---|---|---|---|
Disease duration, mean, and months | 90.77 ± 49.56 | 128 ± 97.48 | 0.306 |
IFX treatment duration, mean, and months | 29.77 ± 17.01 | 38.77 ± 34.60 | 0.511 |
DAS28 at flare and mean | 5.09 ± 1.19 | 4.18 ± 1.67 | 0.189 |
DAS28 after 2 months and mean | 5.68 ± 0.8 | 3.95 ± 1.49 | 0.006 |
csDMARD association and nr (%) | 3 | 9 | 0.028 |
Differences between patient's characteristics were tested by Student's t-test or chi-square test.
IFX: infliximab; csDMARD: conventional synthetic disease modifying antirheumatic drug.
At follow-up, higher DAS28 score was observed in patients with undetectable ETN levels compared to those from group A (7.17 ± 1.21 versus 3.57 ± 1.65, P = 0.003). Similar results were obtained in regards SDAI evolution: mean SDAI in group A was 19.06 versus mean SDAI in group B of 58.73 (P = 0.026). Patients with detectable ETN drug levels had better EULAR response (P = 0.023).
There was a relatively small number of patients treated with ADL. Mean DAS28 after 4 months of treatment from RA flare was 2.20 ± 0.38 in patients with detectable drug levels. Only one patient with undetectable drug level consequently had moderate disease activity at follow-up. No anti-ADL antibodies were found in patients treated with ADL.
4. Discussions
Current recommendation for the management of RA does not address serum biologic drug monitoring in clinical practice [46] even if biologicals possess a large pharmacokinetic variation. Thus, if a better disease control is aimed at measuring drug level seems appropriate [57].
RTX detectable drug level correlated with better clinical response at follow-up. We found a significant difference in RTX drug level at the moment of inadequate response in patients with positive and negative ACPA status. In a number of studies, serum concentration of ACPA and RF decreases during RTX treatment [58, 59], but their relation to RTX serum level has not been studied yet. As is known, there are biomarkers that seem to predict a good EULAR response: no steroid therapy, low lymphocyte count, and high RF level and BAFF levels [60]. Meanwhile, in larger observational cohort study, ACPA was a better biomarker of good EULAR response than RF [61]. Whether RF and/or ACPA positivity predict a better clinical response to RTX still remains to be demonstrated.
In our study, IFX serum drug level at the moment of inadequate response correlated with clinical activity. There was a significant difference in patient's EULAR response at follow-up; patients that had detectable serum drug levels had a better response. The presence of anti-IFX antibodies correlated to disease activity using DAS28 score at baseline; all of the patients with anti-drug antibodies had no EULAR response at follow-up. Methotrexate dose has an impact on INF immunogenicity and appropriate therapeutic approach should be made to reduce its immunogenicity.
As is well known, ETN has the lowest immunogenicity [62] and in our study none of the patients experiencing inadequate response had anti-ETA antibodies. Even though a proportion of them did not have a csDMARD associated there were no differences in serum drug levels. The data obtained in the ADL treated group was not significantly relevant because of the number of patients. But this cannot exclude the utility of serum drug and anti-drug dosing in patients treated with ADL.
Our results showed that evaluation of drug levels in patients that experience inadequate response while being on biologics correlate to their clinical response at follow-up. Thus it can be possible to determine loss of efficacy starting from the first RA exacerbation in patients with stable biologic treatment. This approach can be used in view of a better disease control and appropriate therapeutic decision.
We acknowledge that our study cannot fully demonstrate whether biologic drug dosing is predictive for clinical response and nonresponsiveness. Further studies are essential as this may be an argument for switching to another biologic drug in RA patients.
5. Conclusion
To our knowledge, this is the first study that evaluates biologic drug levels at first inadequate response and their relation to further clinical response in patients with RA. Our study strongly supports the idea that serum drug monitoring should be considered in clinical practice during long-term use of biologic agents. It adds some evidence that immunogenicity has an impact in clinical response in patients with anti-drug antibodies. Measuring drug level and assessing immunogenicity in a RA flare might help to optimize and personalize usage of biological therapies.
Acknowledgments
The authors thank to all patients who voluntarily participated in this cohort. The main authors (Diana Mazilu and Daniela Opris) thank all coauthors for their contribution to this study. ELISA kits for measurement of drug and antidrug levels were sponsored by Pfizer.
Ethical Approval
Ethics Committee of the “Carol Davila” University of Medicine and Pharmacology, Bucharest Romania, approved this study.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Authors' Contribution
Diana Mazilu and Daniela Opris contributed equally to this study.
References
- 1.Sokka T, Kautiainen H, Möttönen T, Hannonen P. Work disability in rheumatoid arthritis 10 years after the diagnosis. The Journal of Rheumatology. 1999;26(8):1681–1685. [PubMed] [Google Scholar]
- 2.Lindhardsen J, Ahlehoff O, Gislason GH, et al. Risk of atrial fibrillation and stroke in rheumatoid arthritis: Danish nationwide cohort study. British Medical Journal. 2012;344(7849) doi: 10.1136/bmj.e1257.e1257 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Solomon DH, Kremer J, Curtis JR, et al. Explaining the cardiovascular risk associated with rheumatoid arthritis: traditional risk factors versus markers of rheumatoid arthritis severity. Annals of the Rheumatic Diseases. 2010;69(11):1920–1925. doi: 10.1136/ard.2009.122226. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hákkinen A, Kautiainen H, Hannonen P, Ylinen J, Arkela-Kautiainen M, Sokka T. Pain and joint mobility explain individual subdimensions of the health assessment questionnaire (HAQ) disability index in patients with rheumatoid arthritis. Annals of the Rheumatic Diseases. 2005;64(1):59–63. doi: 10.1136/ard.2003.019935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Gettings L. Psychological well-being in rheumatoid arthritis: a review of the literature. Musculoskeletal Care. 2010;8(2):99–106. doi: 10.1002/msc.171. [DOI] [PubMed] [Google Scholar]
- 6.Pincus T, Kavanaugh A, Sokka T. Benefit/risk of therapies for rheumatoid arthritis: underestimation of the “side effects” or risks of RA leads to underestimation of the benefit/risk of therapies. Clinical and Experimental Rheumatology. 2004;22(5, supplement 35):S2–S11. [PubMed] [Google Scholar]
- 7.Watson DJ, Rhodes T, Guess HA. All-cause mortality and vascular events among patients with rheumatoid arthritis, osteoarthritis, or no arthritis in the UK General Practice Research Database. The Journal of Rheumatology. 2003;30(6):1196–1202. [PubMed] [Google Scholar]
- 8.Cobb S, Anderson FBW. Length of life and cause of death in rheumatoid arthritis. The New England Journal of Medicine. 1953;249:553–556. doi: 10.1056/NEJM195310012491402. [DOI] [PubMed] [Google Scholar]
- 9.Symmons DPM, Jones MA, Scott DL, Prior P. Longterm mortality outcome in patients with rheumatoid arthritis: early presenters continue to do well. The Journal of Rheumatology. 1998;25(6):1072–1077. [PubMed] [Google Scholar]
- 10.Kvalvik AG, Jones MA, Symmons DPM. Mortality in a cohort of Norwegian patients with rheumatoid arthritis followed from 1977 to 1992. Scandinavian Journal of Rheumatology. 2000;29(1):29–37. doi: 10.1080/030097400750001770. [DOI] [PubMed] [Google Scholar]
- 11.Anderson ST. Mortality in rheumatoid arthritis: do age and gender make a difference? Seminars in Arthritis and Rheumatism. 1996;25:291–296. doi: 10.1016/s0049-0172(96)80015-1. [DOI] [PubMed] [Google Scholar]
- 12.Bathon JM, Martin RW, Fleischmann RM, et al. A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis. The New England Journal of Medicine. 2000;343(22):1586–1593. doi: 10.1056/NEJM200011303432201. [DOI] [PubMed] [Google Scholar]
- 13.Breedveld FC, Weisman MH, Kavanaugh AF, et al. The PREMIER study: a multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment. Arthritis and Rheumatism. 2006;54(1):26–37. doi: 10.1002/art.21519. [DOI] [PubMed] [Google Scholar]
- 14.Klareskog L, van der Heijde D, de Jager JP, et al. Therapeutic effect of the combination of etanercept and methotrexate compared with each treatment alone in patients with rheumatoid arthritis: double-blind randomised controlled trial. The Lancet. 2004;363(9410):675–681. doi: 10.1016/S0140-6736(04)15640-7. [DOI] [PubMed] [Google Scholar]
- 15.Lipsky PE, van der Heijde DM, St Clair EW, et al. Infliximab and methotrexate in the treatment of rheumatoid arthritis. Anti-Tumor Necrosis Factor Trial in Rheumatoid Arthritis with Concomitant Therapy Study Group. The New England Journal of Medicine. 2000;343(22):1594–1602. doi: 10.1056/NEJM200011303432202. [DOI] [PubMed] [Google Scholar]
- 16.Maini R, St Clair EW, Breedveld F, et al. Infliximab (chimeric anti-tumour necrosis factor α monoclonal antibody) versus placebo in rheumatoid arthritis patients receiving concomitant methotrexate: a randomised phase III trial. The Lancet. 1999;354(9194):1932–1939. doi: 10.1016/s0140-6736(99)05246-0. [DOI] [PubMed] [Google Scholar]
- 17.Weinblatt ME, Kremer JM, Bankhurst AD, et al. A trial of etanercept, a recombinant tumor necrosis factor receptor:Fc fusion protein, in patients with rheumatoid arthritis receiving methotrexate. The New England Journal of Medicine. 1999;340(4):253–259. doi: 10.1056/NEJM199901283400401. [DOI] [PubMed] [Google Scholar]
- 18.Weinblatt ME, Keystone EC, Furst DE, et al. Adalimumab, a fully human anti-tumor necrosis factor α monoclonal antibody, for the treatment of rheumatoid arthritis in patients taking concomitant methotrexate: The ARMADA Trial. Arthritis and Rheumatism. 2003;48(1):35–45. doi: 10.1002/art.10697. [DOI] [PubMed] [Google Scholar]
- 19.Keystone EC, Genovese MC, Klareskog L, et al. Golimumab, a human antibody to tumour necrosis factor α given by monthly subcutaneous injections, in active rheumatoid arthritis despite methotrexate therapy: the GO-FORWARD Study. Annals of the Rheumatic Diseases. 2009;68:789–796. doi: 10.1136/ard.2008.099010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.van der Heijde D, Weinblatt M, Landewe R, Goel N, Wells F, Fleischmann RM. Early inhibition of progression of structural damage in certolizumab pegol-treated patients: 16-week efficacy results from RAPID. Annals of the Rheumatic Diseases. 2008;67, supplement 2, article 51 [Google Scholar]
- 21.Emery P, Fleischmann R, Filipowicz-Sosnowska A, et al. The efficacy and safety of rituximab in patients with active rheumatoid arthritis despite methotrexate treatment: results of a phase IIb randomized, double-blind, placebo-controlled, dose-ranging trial. Arthritis and Rheumatism. 2006;54(5):1390–1400. doi: 10.1002/art.21778. [DOI] [PubMed] [Google Scholar]
- 22.Šenolt L, Vencovský J, Pavelka K, Ospelt C, Gay S. Prospective new biological therapies for rheumatoid arthritis. Autoimmunity Reviews. 2009;9(2):102–107. doi: 10.1016/j.autrev.2009.03.010. [DOI] [PubMed] [Google Scholar]
- 23.Singh JA, Furst DE, Bharat A, et al. 2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis. Arthritis Care & Research. 2012;64:625–639. doi: 10.1002/acr.21641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Feltelius N, Fored CM, Blomqvist P, et al. Results from a nationwide postmarketing cohort study of patients in Sweden treated with etanercept. Annals of the Rheumatic Diseases. 2005;64(2):246–252. doi: 10.1136/ard.2004.023473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Van Vollenhoven RF, Carli CC, Bratt JKL. Six year report of the STURE registry for biologicals in rheumatology: satisfactory overall results but plenty of room for improvement. Arthritis & Rheumatology. 2005;52, supplement 9:p. S135. [Google Scholar]
- 26.Khanna R, Sattin BD, Afif W, et al. Review article: a clinician’s guide for therapeutic drug monitoring of infliximab in inflammatory bowel disease. Alimentary Pharmacology & Therapeutics. 2013;38:447–459. doi: 10.1111/apt.12407. [DOI] [PubMed] [Google Scholar]
- 27.Peyrin-Biroulet L, Deltenre P, de Suray N, Branche J, Sandborn WJ, Colombel J-F. Efficacy and safety of tumor necrosis factor antagonists in Crohn’s disease: meta-analysis of placebo-controlled trials. Clinical Gastroenterology and Hepatology. 2008;6(6):644–653. doi: 10.1016/j.cgh.2008.03.014. [DOI] [PubMed] [Google Scholar]
- 28.Afif W, Loftus EV, Jr., Faubion WA, et al. Clinical utility of measuring infliximab and human anti-chimeric antibody concentrations in patients with inflammatory bowel disease. American Journal of Gastroenterology. 2010;105(5):1133–1139. doi: 10.1038/ajg.2010.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Pariente B, Pineton de Chambrun G, Krzysiek R, et al. Trough levels and antibodies to infliximab may not predict response to intensification of infliximab therapy in patients with inflammatory bowel disease. Inflammatory Bowel Diseases. 2012;18(7):1199–1206. doi: 10.1002/ibd.21839. [DOI] [PubMed] [Google Scholar]
- 30.Karmiris K, Paintaud G, Noman M, et al. Influence of trough serum levels and immunogenicity on long-term outcome of adalimumab therapy in Crohn’s disease. Gastroenterology. 2009;137(5):1628–1640. doi: 10.1053/j.gastro.2009.07.062. [DOI] [PubMed] [Google Scholar]
- 31.Velayos FS, Kahn JG, Sandborn WJ, Feagan BG. A test-based strategy is more cost effective than empiric dose escalation for patients with Crohn’s disease who lose responsiveness to infliximab. Clinical Gastroenterology and Hepatology. 2013;11:654–666. doi: 10.1016/j.cgh.2012.12.035. [DOI] [PubMed] [Google Scholar]
- 32.Steenholdt C, Brynskov J, Thomsen O, et al. Individualised therapy is more cost-effective than dose intensification in patients with Crohn’s disease who lose response to anti-TNF treatment: a randomised, controlled trial. Gut. 2013 doi: 10.1136/gutjnl-2013-305279. [DOI] [PubMed] [Google Scholar]
- 33.Vande Casteele N, Gils A, Singh S, et al. Antibody response to infliximab and its impact on pharmacokinetics can be transient. The American Journal of Gastroenterology. 2013;108(6):962–971. doi: 10.1038/ajg.2013.12. [DOI] [PubMed] [Google Scholar]
- 34.Wolbink GJ, Vis M, Lems W, et al. Development of antiinfliximab antibodies and relationship to clinical response in patients with rheumatoid arthritis. Arthritis and Rheumatism. 2006;54(3):711–715. doi: 10.1002/art.21671. [DOI] [PubMed] [Google Scholar]
- 35.Bartelds GM, Krieckaert CLM, Nurmohamed MT, et al. Development of antidrug antibodies against adalimumab and association with disease activity and treatment failure during longterm follow-up. The Journal of the American Medical Association. 2011;305(14):1460–1468. doi: 10.1001/jama.2011.406. [DOI] [PubMed] [Google Scholar]
- 36.Svenson M, Geborek P, Saxne T, Bendtzen K. Monitoring patients treated with anti-TNF-α biopharmaceuticals: assessing serum infliximab and anti-infliximab antibodies. Rheumatology. 2007;46(12):1828–1834. doi: 10.1093/rheumatology/kem261. [DOI] [PubMed] [Google Scholar]
- 37.Pascual-Salcedo D, Plasencia C, Ramiro S, et al. Influence of immunogenicity on the efficacy of long-term treatment with infliximab in rheumatoid arthritis. Rheumatology. 2011;50(8):1445–1452. doi: 10.1093/rheumatology/ker124. [DOI] [PubMed] [Google Scholar]
- 38.Emami-shahri N, Hagemann T. Resistance-the true face of biological defiance. Rheumatology. 2012;51(3):413–422. doi: 10.1093/rheumatology/ker326. [DOI] [PubMed] [Google Scholar]
- 39.Garcês S, Demengeot J, Benito-Garcia E. The immunogenicity of anti-TNF therapy in immune-mediated inflammatory diseases: a systematic review of the literature with a meta-analysis. Annals of the Rheumatic Diseases. 2013;72:1947–1955. doi: 10.1136/annrheumdis-2012-202220. [DOI] [PubMed] [Google Scholar]
- 40.Korswagen LA, Bartelds GM, Krieckaert CLM, et al. Venous and arterial thromboembolic events in adalimumab-treated patients with antiadalimumab antibodies: a case series and cohort study. Arthritis and Rheumatism. 2011;63(4):877–883. doi: 10.1002/art.30209. [DOI] [PubMed] [Google Scholar]
- 41.van Schouwenburg PA, Bartelds GM, Hart MH, Aarden L, Wolbink GJ, Wouters D. A novel method for the detection of antibodies to adalimumab in the presence of drug reveals “hidden” immunogenicity in rheumatoid arthritis patients. Journal of Immunological Methods. 2010;362(1-2):82–88. doi: 10.1016/j.jim.2010.09.005. [DOI] [PubMed] [Google Scholar]
- 42.Hart MH, de Vrieze H, Wouters D, et al. Differential effect of drug interference in immunogenicity assays. Journal of Immunological Methods. 2011;372(1-2):196–203. doi: 10.1016/j.jim.2011.07.019. [DOI] [PubMed] [Google Scholar]
- 43.Garcês S, Antunes M, Benito-Garcia E, Canas da Silva J, Aarden L, Demengeot J. A preliminary algorithm introducing immunogenicity assessment in the management of patients with RA receiving tumour necrosis factor inhibitor therapies. Annals of the Rheumatic Diseases. 2013 doi: 10.1136/annrheumdis-2013-203296. [DOI] [PubMed] [Google Scholar]
- 44.Arnett FC, Edworthy SM, Bloch DA, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis and Rheumatism. 1988;31(3):315–324. doi: 10.1002/art.1780310302. [DOI] [PubMed] [Google Scholar]
- 45.Aletaha D, Neogi T, Silman AJ, et al. 2010 rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism Collaborative Initiative. Arthritis & Rheumatism. 2010;62(9):2569–2581. doi: 10.1002/art.27584. [DOI] [PubMed] [Google Scholar]
- 46.Smolen JS, Aletaha D, Bijlsma JW, et al. Treating rheumatoid arthritis to target: recommendations of an international task force. Annals of the Rheumatic Diseases. 2010;69(4):631–637. doi: 10.1136/ard.2009.123919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Ionescu R. Ghiduri de Diagnostic si Tratament in Reumatolgie. 2013. [Google Scholar]
- 48.Bingham CO, III, Pohl C, Woodworth TG, et al. Developing a standardized definition for disease “flare” in rheumatoid arthritis (OMERACT 9 special interest group) The Journal of Rheumatology. 2009;36(10):2335–2341. doi: 10.3899/jrheum.090369. [DOI] [PubMed] [Google Scholar]
- 49.Van der Maas A, den Broeder AA. Measuring flares in rheumatoid arthritis. (Why) do we need validated criteria? The Journal of Rheumatology. 2014;41:189–191. doi: 10.3899/jrheum.131217. [DOI] [PubMed] [Google Scholar]
- 50.Gorovits B. Antidrug antibody assay validation: industry survey results. AAPS Journal. 2009;11(1):133–138. doi: 10.1208/s12248-009-9091-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Plasencia C, Pascual-Salcedo D, Nuño L, et al. Influence of immunogenicity on the efficacy of longterm treatment of spondyloarthritis with infliximab. Annals of the Rheumatic Diseases. 2012;71(12):1955–1960. doi: 10.1136/annrheumdis-2011-200828. [DOI] [PubMed] [Google Scholar]
- 52.Llinares-Tello F, de Salazar JR, Gallego JM, et al. Analytical and clinical evaluation of a new immunoassay for therapeutic drug monitoring of infliximab and adalimumab. Clinical Chemistry and Laboratory Medicine. 2012;50(10):1845–1847. doi: 10.1515/cclm-2012-0050. [DOI] [PubMed] [Google Scholar]
- 53.van Schouwenburg PA, van de Stadt LA, de Jong RN, et al. Adalimumab elicits a restricted anti-idiotypic antibody response in autoimmune patients resulting in functional neutralisation. Annals of the Rheumatic Diseases. 2013;72(1):104–109. doi: 10.1136/annrheumdis-2012-201445. [DOI] [PubMed] [Google Scholar]
- 54.Plasencia C, Pascual-Salcedo D, García-Carazo S, et al. The immunogenicity to the first anti-TNF therapy determines the outcome of switching to a second anti-TNF therapy in spondyloarthritis patients. Arthritis Research & Therapy. 2013;15(4, article R79) doi: 10.1186/ar4258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Plasencia C, Pascual-Salcedo D, Alcocer P, et al. The timing of serum infliximab loss, or the appearance of antibodies to infliximab (ATI), is related with the clinical activity in ATI-positive patients with rheumatoid arthritis treated with infliximab. Annals of the Rheumatic Diseases. 2013;72:1888–1890. doi: 10.1136/annrheumdis-2013-203353. [DOI] [PubMed] [Google Scholar]
- 56.Ruiz-Argüello B, del Agua AR, Torres N, Monasterio A, Marti'nez A, Nagore D. Comparison study of two commercially available methods for the determination of infliximab, adalimumab, etanercept and anti-drug antibody levels. Clinical Chemistry and Laboratory Medicine. 2013;51(12):e287–e289. doi: 10.1515/cclm-2013-0461. [DOI] [PubMed] [Google Scholar]
- 57.Krieckaert CL, Nair SC, Nurmohamed MT, et al. Personalised treatment using serum drug levels of adalimumab in patients wih rheumatoid arthritis: an evaluation of costs and effects. Annals of the Rheumatic Diseases. 2013 doi: 10.1136/annrheumdis-2013-204101. [DOI] [PubMed] [Google Scholar]
- 58.Thurlings RM, Vos K, Wijbrandts CA, Zwinderman AH, Gerlag DM, Tak PP. Synovial tissue response to rituximab: mechanism of action and identification of biomarkers of response. Annals of the Rheumatic Diseases. 2008;67(7):917–925. doi: 10.1136/ard.2007.080960. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Teng YKO, Levarht EWN, Hashemi M, et al. Immunohistochemical analysis as a means to predict responsiveness to rituximab treatment. Arthritis and Rheumatism. 2007;56(12):3909–3918. doi: 10.1002/art.22967. [DOI] [PubMed] [Google Scholar]
- 60.Ferraccioli G, Tolusso B, Bobbio-Pallavicini F, et al. Biomarkers of good EULAR response to the B cell depletion therapy in all seropositive rheumatoid arthritis patients: clues for the pathogenesis. PLoS One. 2012;7 doi: 10.1371/journal.pone.0040362.e40362 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Chatzidionysiou K, Lie E, Nasonov E, et al. Highest clinical effectiveness of rituximab in autoantibody-positive patients with rheumatoid arthritis and in those for whom no more than one previous TNF antagonist has failed: pooled data from 10 European registries. Annals of the Rheumatic Diseases. 2011;70(9):1575–1580. doi: 10.1136/ard.2010.148759. [DOI] [PubMed] [Google Scholar]
- 62.Hoshino M, Yoshio T, Onishi S, Minota S. Influence of antibodies against infliximab and etanercept on the treatment effectiveness of these agents in Japanese patients with rheumatoid arthritis. Modern Rheumatology. 2012;22(4):532–540. doi: 10.1007/s10165-011-0567-8. [DOI] [PubMed] [Google Scholar]