- Research article
- Open Access
Methotrexate efficacy, but not its intolerance, is associated with the dose and route of administration
Pediatric Rheumatology volume 14, Article number: 36 (2016)
There is a lack of published evidence on the importance of methotrexate (MTX) dose and route of administration on both its efficacy and adverse events in children with Juvenile Idiopathic Arthritis (JIA). We aimed to document our clinical practice based on the treat-to-target approach in order to support the concept that better therapeutic effect achieved with an optimal dose of parenteral MTX is associated with clinically acceptable adverse effects comparable to those reported for oral treatment.
Study inclusion criteria were indication of new MTX therapy for active arthritis in confirmed JIA patients younger than 18 years. Eligible patients were evaluated prospectively every 3 months for 1 year using standardized instruments for treatment response (American College of Rheumatology Pediatric (ACRPedi) response, Juvenile Arthritis Disease Activity Score (JADAS) 71, Clinically Inactive Disease (CID)) and adverse events (laboratory monitoring, Methotrexate Intolerance Severity Score (MISS)). MTX responders had to achieve at least ACRPedi 70 response. MTX intolerance was defined by MISS ≥ 6.
In 45/55 patients (81.8 %) MTX was started as subcutaneous injection. The initial median weekly dose was 14.4 mg/m2 in parenteral and 11.7 mg/m2 in oral administration. MTX therapy was effective in the level of ACRpedi70 and CID in 50.9 % and 30.9 % of patients at month 6 and in 70.9 % and 56.4 % after 12 months of the treatment, respectively. MTX intolerance at 6 and 12 months was noted in 25.5 % and 30.6 %, respectively. Management of intolerance included change in the dose and/or route of administration, education and councelling. Adverse events led to MTX withdrawal in 5 patients (9 %) due to toxicity (n = 3) and intolerance (n = 2). We did not find any significant predictive factors for either MTX therapeutic response or intolerance.
Subcutaneous MTX weekly dose around 15 mg/m2 is associated not only with a high response rate within the first 12 months of treatment, but also with a relatively low rate of significant adverse effects that would lead to the treatment termination. It allows early recognition of MTX non-responders and addition of biologic therapy. Sustainability of therapeutic effect and longer-term evolution of adverse events will be addressed by an ongoing extension of the study.
Over the last decades low-dose weekly methotrexate (MTX) has been commonly used in the treatment of juvenile idiopathic arthritis (JIA) . It has become an essential component of various clinical guidelines and recommendations as a first-line disease-modifying drug for disease unresponsive to nonsteroidals (NSAIDs) and/or intraarticular corticosteroids [2–4].
MTX efficacy has been reported mainly in polyarticular-course JIA, though its extent varies [5, 6]. Differences in drug dosing and route of administration as well as in the method of efficacy assessment hamper inter-study comparisons. Most commonly, American College of Rheumatology Pediatric (ACRpedi) response criteria have been used to define various levels of therapeutic effect . More recently, a composite measure of disease activity (Juvenile Arthritis Disease Activity Index, JADAS) and its cut-off values for various disease status have been defined . Among factors influencing inter-patient heterogeneity of treatment response, polymorphisms of genes involved in MTX metabolic pathways [9–15], disease phenotype and its previous duration and several biomarkers have been reported [16–20]. Moreover, factors related to MTX absorption and kinetics have also been shown to influence treatment efficacy [21–25].
Evaluation of the presence, type and severity of drug adverse events forms a natural part of therapeutic monitoring. Low-dose MTX has a variety of adverse effects. These include features of MTX antiproliferative effect which are mostly related to its post-dose concentrations [26–30]. MTX affects rapidly dividing cells of gastrointestinal (GI) tract causing nausea and/or vomiting and bone marrow leading to cytopenia. Mechanisms of hepatic and central nervous system (CNS) toxicity are more complex and include elevation of liver enzymes, headaches and behavioral changes [31, 32]. In addition to post-treatment complaints anticipatory and associative symptoms have been described [33–35]. Patients report presence of gastrointestinal symptoms or behavioral changes (cry, irritation, refusal to take the drug) already before or at the time of MTX administration (anticipatory intolerance) or even when just thinking about it (associative intolerance). They appear to be more commonly associated with parenteral route of MTX administration and often lead to precautious termination of otherwise safe and effective treatement [36, 37]. Therefore monitoring of MTX adverse events requires not only regular blood tests for hepatic and marrow toxicity, but also directed questioning to detect subjective complaints.
This study was driven by the lack of published evidence on the importance of MTX dose and route of administration on both its efficacy and various types of adverse events. We aimed to thoroughly document our clinical practice based on the treat-to-target approach in order to prove the concept that better therapeutic effect achieved with the higher dose of parenteral MTX is associated with clinically acceptable adverse effects comparable to those reported in published series using oral treatment.
Patients and study protocol
Consecutive patients were recruited prospectively from the paediatric rheumatology clinic population of the Department of Paediatrics and Adolescent Medicine, 1st Faculty of Medicine, Charles University in Prague, between October 2013 and January 2015.
This was a sub-study of a large project running at the Unit aim of which was to prospectively collect clinical data on all consecutive JIA patients starting new treatments for active disease. The project was approved by the Local Research Ethics Committee of the General University Hospital in Prague and informed consent was obtained from the patients and/or their legal guardians, as appropriate. To become eligible patients must have had a definitive diagnosis of JIA according to the ILAR criteria  and exhibit active disease requiring either initiation of treatment for new-onset JIA or for the disease relapse. Active disease was defined by the presence of at least one joint with synovitis. Treatment options were: intra-articular triamcinolone hexacetonide, MTX, sulphasalazine, TNF-inhibitors and tocilizumab. At our Unit the treatment plan guided by the recently published ACR recommendations [2, 3] is always individually tailored to patient needs according to the treating physician. Only patients starting the MTX treatment are included in this report. The MTX therapeutic strategy is based on the following principles: 1. Early start, 2. MTX dose around 15 mg/m2/week administered parenterally using pre-filled syringes (MTX concentration 50 mg/ml), 3. Folic acid supplementation 5–10 mg once weekly 24–48 h after MTX dose, 4. The same dose which has induced disease inactivity is maintained for the minimum of 1 year if no clinically significant adverse events occur. Non-responders at 3–6 months change their treatment, usually by adding a biologic drug. Oral MTX in one weekly single dose is rarely considered in older children with relatively mild disease. Clinical and laboratory data and patient-reported outcomes are recorded within the interval of ± 2 weeks of the first MTX administration and then in 3-monthly intervals.
Assessment of treatment efficacy
Treatment effect was evaluated by using two standardized methodologies for JIA activity assessment: ACR Pedi (The American College of Rheumatology) and JADAS (the Juvenile Arthritis Disease Activity Score). ACR Pedi uses the core-set of 6 disease activity variables (active joint count, limited joint count, physician global assessment of disease activity, parent/patient global assessment of the patient's well-being, Childhood Health Assessment Questionnaire and ESR/CRP) on 2 distinct occasions resulting in the defined improvement rates of ACR Pedi 30, 50, 70 and 90. These rates are defined as improvement of at least 3 out of 6 variables by a minimum of 30, 50, 70 or 90 % and no more than one of the resulting ones deteriorating by more than 30 % . Good clinical response to MTX was defined as reaching the minimum of ACR Pedi 70. JADAS is a numeric score resulting from the values of 4 measures: active joint count (from 10, 27 or 71 joints), physician's global assessment of disease activity (10 cm VAS), parent/patient global assessment of overall well-being (10 cm VAS) and normalized ESR rate (0–10) . JADAS-71 (score range 0–101) was chosen for this study. Additionally, disease state at 6 and 12 months was assessed according to the JADAS cutoff values as inactive disease (≤1) or minimally active disease (≤2 for oligoarthritis and ≤3.8 for polyarthritis) and high disease activity (4.2 for oligoarthritis and 10.5 for polyarthritis) [39–42].
Complete treatment response was also defined applying the Wallace criteria as the presence of inactive disease (clinically inactive disease, CID). CID is defined by an absence of active synovitis or other active JIA features (incl. uveitis, fever, rash, serositis, hepatosplenomegaly, lymhadenopathy attributable to JIA), normal ESR or CRP, the lowest possible physician global evaluation of disease activity and absence of significant morning stiffness (duration ≤15 min) [43–45].
Assessment of MTX treatment adverse events
For the purpose of this study MTX adverse events were divided into toxicity and intolerance. Toxic adverse events were further assessed as measurable toxicity (increase of at least one liver transaminase above 2-times of upper normal limit (ULN) or significant cytopenia or anaemia) and patient-reported toxicity defined as patient complaints developing after MTX administration (gastrointestinal symptoms - abdominal pain, nausea, vomiting, oral ulcers, injection site reaction). Conditioned response to MTX-associated toxicity was defined as anticipatory intolerance when gastrointestinal (GI) complaints were present at the time of MTX administration, associative intolerance was considered when GI complaints occurred when thinking about MTX administration.
On top of that behavioral symptoms at the time of MTX administration were also recorded. Patient-reported symptoms were captured at every visit using the Czech adaptation of the Methotrexate Intolerance Severity Score (MISS), which defines MTX-intolerant patient by the presence of at least 6 out of 36 points with at least 1 point on anticipatory and/or associative and/or behavioral symptoms .
Continuous and categorical variables were described using median with 25th and 75th percentile and relative frequencies. Mann–Whitney U test was used when assessing statistical significance of difference in continuous variables between two groups (when comparing more than two samples Kruskal-Wallis test with post-hoc Bonferroni correction was applied). Statistical significance of dependence between categorical variables was assessed with Fisher exact test. Time to treatment response was analyzed using Kaplan-Meier survival analysis method. Univariate logistic regression model was applied to measure association of baseline characteristics with occurrence of MTX intolerance (or treatment response). Level of statistical significance was set to 0.05 in all analyses.
Characteristics of the patient cohort
Total of 107 patients fulfilled the study inclusion criteria during the 16-month recruitment period. In 58 children MTX therapy was initiated. Out of them 55 expressed their consent with the study participation. Their characteristics are summarized in Table 1. Their median age at study entry was 5.3 years (IQR 2.8;10.6), at disease onset 4.8 years (IQR 2.2; 10.0), disease duration was 3.8 months (IQR 2.5;6.4). The distribution of JIA ILAR onset subtypes at study entry was: oligoarthritis 38.2 % (N = 21) (persistent 32.7 % (N = 18), extended 5.5 % (N = 3)), polyarthritis 45.5 % (N = 25), enthesitis- related arthritis 5.5 % (N = 3), psoriatic arthritis 1.8 % (N = 1), systemic arthritis 9.1 % (N = 5). New onset disease was present in 48 patients (87.3 %), 7 patients had disease relapse. In these patients median interval from the previous medication withdrawal to the relapse was 10.5 months (IQR 6.0; 15.0). Median initial JADAS score was 12.0 (IQR 8.5; 20.2) reflecting active disease with the median number of joints with active arthritis of 5 (IQR 3; 6). High disease activity (JADAS cutoff values 4.2 for oligoarthritis and 10.5 for polyarthritis) was present in 40 children (72.7 %). Median JADAS in those who developed polyarticular course of the disease (regardless JIA onset subtype, N = 45) was 14 (ICQ 10.0; 20.4), patients with persistent oligoarthritis (at 12 months of follow-up, No =10) had median JADAS of 5.6 (ICQ 5.0; 8.5). Concomitant medication at the start of MTX therapy included systemic (oral) corticosteroids in 9 patients (16,4 %) (for systemic symptoms n = 4, resistant uveitis n = 3, severe polyarthritis n = 2) and intraarticular corticosteroids (within 1 month before or after MTX start) in 21 patients (38,2 %).
In 45 patients (81,8 %) MTX was started as once weekly subcutaneous injection, 10 patients received oral tablets (Table 1). There was no significant difference in demographic or disease parameters between the groups apart from the age at MTX start which was higher in patients starting oral treatment (median 14,0 years (IQR 11.8; 15.9) when compared to patients treated parenterally (median 4,1 years (IQR 2.6; 7.8) (p < 0,001). Parenteral MTX was administered in the median weekly dose of 14.4 mg/m2 (IQR 13.3; 15.9), oral MTX dose was 11.7 (8.3; 12.5) (p < 0,001).
Table 2 summarizes treatment changes, their timing and respective disease activity during the follow-up. MTX dose (median (IQR)) was increased from 12.1 (11.1; 13.7) mg/m2 at study entry to 14.9 (13.6; 15.6) and 13.8 (12.4; 15.8) mg/m2 at 6 and 12 months, respectively, in 18 patients (32.7 %). In 20 children (36.4 %) it was decreased from 14.3 (12.4; 16.1) to 13.7 (12.2; 15.2) and 10.5 (8.8; 12.8) mg/m2 at 6 and 12 months, respectively. Other treatment modifications included change in the route of administration (n = 13; 23.6 %), withdrawal (n = 5; 9.1 %), addition of biological therapy (n = 14; 25.5 %). Increased dose and change from oral to parenteral application were always due to the persistence of active disease. On the other hand, change from parenteral to oral administration and MTX dose reduction were triggered by combinations of MTX toxicity and intolerance on the background of the decreasing disease activity (Table 2). Treatment changes resulted in the median MTX dose of 14.2 mg/m2 (IQR 13.1;15.4) at 6 months and 13.7 mg/m2 (IQR 11.5;14.4) at 12 months for the whole cohort. At month 12 from 50 patients who were still receiving MTX only 9 had oral tablets.
All 14 patients who received biologic therapy either failed to achieve ACRpedi50 response (n = 11) and/or had resistant uveitis (n = 4). Their median JADAS71 at the time of treatment change was 15.8 (ICQ 6.50; 13.00). Addition of biologics (etanercept = 8, adalimumab = 4, tocilizumab = 2) occured after the median duration of MTX therapy of 3.8 (ICQ 4.0; 8.8) months.
Treatment efficacy and disease activity assessments
MTX therapy was effective in the level of ACRpedi70 and 90 in 50.9 % and 42.9 % of patients at month 6 and in 70.9 % and 63.6 % after 12 months of the treatment, respectively. Clinically inactive disease was reached in 17 (30.9 %) patients at month 6 and in 31 (56.4 %) patients at month 12. There was no difference in the time to inactivity between various JIA subtypes. Patients who received biologics (n = 14) were considered non-responders to MTX from the time point of starting the biologic including 4 children who achieved CID after biologic medication was added to MTX who were excluded from the evaluation of disease inactivity. Total of 61.8 % patients reached low disease activity according to published JADAS cutoff values for oligo and polyarthritis (Table 3).
Table 3 shows evolution of therapeutic response during 1-year follow-up as expressed by different disease activity measures. There was no significant difference in the proportion of patients who reached high levels of response when measured by either JADAS value (=0) or by fullfilling the CID criteria. Neither the rate or extent of therapeutic response were influenced by JIA onset subtype or by the route of MTX administration (data not shown). Figure 1 illustrates treatment response as expressed by JADAS71 values in persistent oligoarthritis and polyarticular-course JIA patients. Logistic regression analysis of demographic data, disease and treatment characteristics did not reveal any variable that would significantly influence the likelihood of therapeutic response (data not shown).
MTX toxicity and intolerance
During the 12 month follow-up measurable toxicity of MTX was recorded in 8 patients (15.4 %): elevation of transaminases in 7 patients and cytopenia in 1 patient. In 3 cases these adverse events led to MTX withdrawal while in the remaining 5 children results normalised after the short treatment interruption or MTX dose reduction. None of the patients reported significant oral ulcers or injection site reaction.
Presence of patient-reported GI toxicity, associative/anticipatory intolerance and behavioral symptoms is summarized in Table 4. Only 11/55 patients (20 %) reported no adverse events throughout the observational period (MISS = 0 at every visit). Intolerance (MISS ≥ 6) slowly developed during the initial months of the treatment and was present in the maximum of 25.5 % of patients at 6 months and remained relatively stable thereafter (30.6 % at 12 months). This cut-off MISS value for the definition of intolerance was reached at least once in 25/55 children (45.5 %). Concomitant treatment with biologics did not have any significant impact on the MISS at 12 months (data not shown). In the majority of cases intolerance was managed to the patient and family satisfaction by treatment modifications and various other actions and their combinations: change in the route and/or timing of MTX administration, MTX dose reduction, addition of antiemetics, councelling. MTX withdrawal was the ultimate solution in 2 patients only (8 %).
Behavioral symptoms were noted in at least one category in all intolerant patients, but they were present also in 27 (49 %) patients with the MISS lower than 6, regardless the route of MTX administration. The mean MTX dose in intolerant patients was not significantly different from that of tolerant ones (14.2 vs 13,4 mg/m2, OR (95 % CI) = 1,15(0.94;1,40), p = 0,612) (Table 5).
There were no serious adverse events (e.g. infections, pulmonary toxicity) that would require hospital admission throughout the study period. Logistic regression analysis did not demonstrate any significant associations of MTX intolerance with the patient, disease and treatment variables (Table 6). There was a trend towards increased odds for MTX intolerance in patients treated with parenteral MTX (OR (95 % CI) = 2,44 (0,56;10,65), p = 0,236), polyarticular-course of JIA (OR (95 % CI) = 1,43 (0,36; 5,78), p = 0,612) and higher age at MTX start (OR (95 % CI = 1,45 (0,48; 4,47), p = 0,505). Potential predictive factors of good MTX tolerance were higher CHAQ values, shorter interval from disease onset to treatment and male gender (Table 6).
We have reported disease outcome in a single-centre cohort of patients with early JIA (median disease duration 3.8 months) during the first 12 months of MTX treatment. This prospective observational study was triggered by the lack of published evidence on the advantages of the parenteral versus oral route of MTX administration during the induction of remission therapy of JIA. Notably, we documented treatment efficacy using up-to-date standard disease assessments along systematic evaluation of MTX adverse events including conditioned effects like associative and anticipatory intolerance. We have shown that subcutaneous MTX weekly dose around 15 mg/m2 is associated not only with a response rate of ACRpedi 70 in over 70 % of patients, but also with a very low rate of significant adverse effects that would lead to the treatment termination.
An advent of cytokine inhibitors as well as better handling of standard JIA treatments like MTX have shifted our therapeutic target from reduction of disease activity to its complete elimination defined as disease inactivity and remission [46, 47]. With the constantly growing body of evidence on the biology of chronic arthritis it has become evident that time plays an important role in our ability to induce disease inactivity: The shorter disease duration before treatment onset and the more intensive therapeutic regimen used, the bigger is the chance to achieve sustained remission [19, 46, 47]. Such a treat-to-target approach has changed the way we use MTX now from the slow dose-escalation regime to the more aggressive treatment using the optimal effective dose established by Ruperto et al. at 15 mg/m2  from the very beginning. Moreover, pharmacokinetic studies suggesting better bioavailability of parenteral against oral MTX [25, 26] have led us to starting MTX treatment in majority of patients in the form of subcutaneous injections. This approach allows for early assessment of the patient's potential to respond to treatment and to introduce biologic therapy in non-responders as early as within 3–6 months from starting MTX.
Indeed, in our cohort of 55 patients starting MTX only 10 (18.2 %) received oral tablets. The difference in the initial MTX dose and route of administration from some recently published series is illustrated in Table 7. Treatment response at 6 and/or 12 months is expressed by the percentage of patients achieving ACRpedi70 and/or CID. Proportion of MTX responders at 6 months is similar across most of the studies ranging from 38 to 56 % of patients [33, 44–53], similar to our results. Only a few studies provide information on the rate of inactive disease . The higher rate of CID in our cohort (30.9 %) at 6 months when compared to the studies by Ruperto et al. (12 %)  and Wallace et al. (23.3 %)  could be explained by higher MTX dose and shorter prior disease duration in our patients. Although the dose of 15 mg/m2 is close to 0.5 mg/kg in older children, dosing per body weight unit in younger individuals ends up with a lower calculated dose. We believe these reasons together with the parenteral route of MTX administration apply also to the higher rate of responders in our cohort after 1 year of parenteral MTX therapy which exceeded 70 % of patients with the total of 56.4 % reaching CID (Table 3). Additionally, the variability of results in different studies also reflects differences in their design (retrospective analysis from the registry, prospective observational, prospective treatment trial).
Multiple studies have dealt with potential biomarkers of response to MTX that could inform our therapeutic decision-making and lead to early introduction of other treatments in suspected non-responders, reviewed by Dijkhuizen . Among these high serum concentration of MRP8/14 protein at baseline  and long-chain MTX polyglutamates at 3 months of the treatment  predicted a favourable response to MTX. From genetic factors single-nucleotide polymorphisms of genes involved in MTX metabolic pathways and some novel candidate genes have been suggested, though their relevance is yet to be confirmed [53–55].
The spectrum of adverse events of MTX therapy has expanded by the recognition and systematic evaluation of so called conditioned response in the form of anticipatory and associative intolerance [34, 35, 56–58]. In this study we have attempted to distinguish toxic adverse events limited to laboratory changes and post-dose GI symptoms from the intolerance featuring GI symptoms around MTX administration (anticipatory) and when thinking about MTX (associative) using a previously validated scoring system MISS  (Table 5). In addition, behavioral symptoms at MTX administration were also systematically recorded.
Proportion of patients who featured measurable toxic adverse events of transaminase elevation and/or cytopenia was similar to published series [32, 58–60] and was mild and easy to manage in most cases. Presence of patient-reported GI toxicity as well as intolerance and behavioral symptoms were frequent (Table 4). MTX intolerance (MISS ≥ 6) in at least one visit during the 12 months of treatment was recorded in 45.5 % of our patients. This figure is similar to that reported by Bulatovič and van Dijkhuizen (50.5 % and 41.5 %, respectively) despite the fact that our patients received higher MTX doses (14.2 mg/m2 versus 10.2 and 9.9 mg/m2, respectively) administered parenterally in most cases [5, 34]. This finding does not support the presence of direct relationship between MTX dose and route of administration and its intolerance. This is in agreement with our previous observation where higher doses of MTX associated with increased intracellular MTX concentrations did not lead to an increased rate of MTX toxicity .
Severity of MTX intolerance is difficult to assess due to the subjective nature of patient-reported symptoms. Therefore we believe that an impact of reported adverse events on the treatment itself should serve as the main measure of their clinical significance. Despite the high frequency of complaints in our study they eventually led to MTX withdrawal in 2 patients only. It is our impression that this favourable outcome was associated with the systematic approach to MTX-related complaints in our clinics. MISS form was administered along other patient-reported questionnaires to every patient at routine follow-up visits by the nurse specialist who checked its completion and then discussed with the treating physician who reviewed the ticked items with the patient and/or the accompanying parent and suggested potential solutions tailored to the individual patient characteristics and needs. These discussions covered also the analysis of the risk/benefit ratio of MTX therapy and re-assessment of the future treatment plan. Such a systematic parent/patient education and re-assurance served as an additional component of intolerance management. In the light of the massive evidence on the efficacy and tolerance of biologics, MTX adverse effects are becoming more visible than 20 years ago when therapeutic options for JIA were limited. Moreover, incorporation of patient-reported outcomes into the routine disease assessment has led to better appreciation of an impact of subjective complaints including drug intolerance on the patient and family health-related quality of life.
The relatively short duration of follow-up reported here did not allow for assessment of the sustainability of treatment response as well as the long-term evolution of adverse events. Moreover, direct comparison of treatment efficacy and adverse events between patients treated with oral versus parenteral MTX was not possible due to relatively small numbers of patients, mainly those treated orally. Small patient number also contributed to the inability to detect any significant variables associated with either treatment response or presence of adverse events (Table 6). Although JIA treatment strategy has been established at our Unit the study retained an observational character where therapy was based on the treating physician's decision. Therefore systematic stratification of patients into more homogeneous treatment groups that would improve our ability to analyze treatment variables was not possible.
As long as the reliable and widely accessible system of prediction of MTX efficacy and intolerance is not available, optimal clinical approach to MTX therapy remains of upmost importance. This study brings additional evidence for the high efficacy of MTX especially in early disease and underlines importance of using the dose around 15 mg/m2 administered parenterally in order to evaluate treatment response early in the disease course. Such a treatment strategy does not appear to increase the rate and severity of MTX adverse events when compared to oral treatment using lower doses. Limited by short duration of follow-up and relatively small patient number true significance of our findings has yet to be confirmed through the ongoing extension of the study.
- ACR Pedi:
American College of Rheumatology Pediatric
Clinically Inactive Disease
Childhood Health Assessment Questionnaire
Erythrocyte Sedimentation Rate
Intraarticular triamcinolone hexacetonide
Juvenile Arthritis Disease Activity Score
Juvenile Idiopathic Arthritis
Methotrexate Intolerance Severity Score
Non-steroidal Anti-Inflammatory Drugs
Ravelli A, Martini A. Juvenile idiopathic arthritis. Lancet. 2007;369(9563):767–78.
Beukelman T, Patkar NM, Saag KG, Tolleson-Rinehart S, Cron RQ, DeWitt EM, et al. 2011 American College of Rheumatology recommendations for the treatment of juvenile idiopathic arthritis: initiation and safety monitoring of therapeutic agents for the treatment of arthritis and systemic features. Arthritis Care Res (Hoboken). 2011;63(4):465–82. doi:10.1002/acr.20460.
Ringold S, Weiss PF, Beukelman T, DeWitt EM, Ilowite NT, Kimura Y, et al. 2013 Update of the 2011 American College of Rheumatology Recommendations for the Treatment of Juvenile Idiopathic Arthritis Recommendations for the Medical Therapy of Children With Systemic Juvenile Idiopathic Arthritis and Tuberculosis Screening Among Children Receiving Biologic Medications. Arthritis Rheum. 2013;65(10):2499–512. doi:10.1002/art.38092.
Dueckers G, Guellac N, Arbogast M, Dannecker G, Foeldvari I, Frosch M, et al. Evidence and consensus based GKJR guidelines for the treatment of juvenile idiopathic arthritis. Clin Immunol. 2012;142(2):176–93.
van Dijkhuizen EH, Wulffraat NM. Prediction of methotrexate efficacy and adverse events in patients with juvenile idiopathic arthritis: a systematic literature review. Pediatr Rheum. 2014;12:51. doi:10.1186/1546-0096-12-51.
Vilca I, Munitis PG, Pistorio A, Ravelli A, Buoncompagni A, et al. Pediatric Rheumatology International Trials Organisation (PRINTO): Predictors of poor response to methotrexate in polyarticular-course juvenile idiopathic arthritis: analysis of the PRINTO methotrexate trial. Ann Rheum Dis. 2010;69:1479–83. doi:10.1136/ard.2009.120840.
Giannini EH, Ruperto N, Ravelli A, Lovell DJ, Felson DT, Martini A. Preliminary definition of improvement in juvenile arthritis. Arthritis Rheum. 1997;40:1202–9.
Consolaro A, Ruperto N, Bazso A, Pistorio A, Magni-Manzoni S, Filocamo G, et al. Paediatric Rheumatology International Trials Organisation. Development and Validation of a Composite Disease Activity Score for Juvenile Idiopathic Arthritis. Arthritis Rheum. 2009;61(5):658–66. doi:10.1002/art.24516.
Dervieux T, Greenstein N, Kremer J. Pharmacogenomic and metabolic biomarkers in the folate pathway and their association with methotrexate effects durin dosage escalation in rheumatoid arthritis. Arthritis Rheum. 2006;54(10):3095–102.
Becker ML, Van Haandel L, Gaedick R, et al. Analysis of methotrexate polyglutamates in patients with juvenile idiopathic arthritis: effect of route of administration on variability of intracellular methotrexate polyglutamate concentrations. Arthritis Rheum. 2010;62:1803–12.
Hroch M, Tukova J, Dolezalova P, Chladek J. An improved high-performance liquid chromatography method for quantification of methotrexate polyglutamates in red blood cells of children with juvenile idiopathic arthritis. Biopharm Drug Dispos. 2009;30(3):138–48. doi:10.1002/bdd.654.10.1002/art.38092.
Hinks A, Moncrieffe H, Martin P, et al. Association of the five-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. Ann Rheum Dis. 2011;70(8):1395–400.
Bulatovic M, Heijstek M, Van Dijkhuizen EH, Wulffraat N, Pluijm S, De Jonge R. Prediction of clinical nonresponse to methotrexate treatment in juvenile idiopathic arthritis. Ann Rheum Dis. 2012;71(9):1484–9.
Dolezalova P, Krijt J, Chladek J, Nemcova D, Hoza J. Adenosine and methotrexate polyglutamate concentrations in patients with juvenile arthritis. Rheumatology (Oxford). 2005;44(1):74–9.
Tukova J, Chladek J, Hroch M, Nemcova D, Hoza J, Dolezalova P. 677TT genotype is associated with elevated risk of methotrexate (MTX) toxicity in juvenile idiopathic arthritis: treatment outcome, erythrocyte concentrations of MTX and folates, and MTHFR polymorphisms. J Rheumatol. 2010;37:2180–6.
Ravelli A, Viola S, Migliavacca D, Ruperto N, Pistorio A, Martini A. The oligoarticular subtype is the best predictor of methotrexate efficacy in juvenile idiopathic arthritis. J Pediatr. 1999;135:316–20.
Wallace CA, Ruperto N, Giannini E. Childhood Arthritis and Rheumatology Research Alliance; Pediatric Rheumatology International Trials Organization; Pediatric Rheumatology Collaborative Study Group. Preliminary criteria for clinical remission for select categories of juvenile idiopathic arthritis. J Rheumatol. 2004;31(11):2290–4.
Albers HM, Wessels JA, van der Straaten RF, Brinkman DM, Suijlekom-Smit LW, Kamphuis SS, et al. Time to treatment as an important factor for the response to methotrexate in juvenile idiopathic arthritis. Arthritis Rheum. 2009;61(1):46–51. doi:10.1002/art.24087.
Vilca I, Munitis PG, Pistorio A, Ravelli A, Buoncompagni A, Bica B, et al. Pediatric Rheumatology International Trials Organisation (PRINTO): Predictors of poor response to methotrexate in polyarticular-course juvenile idiopathic arthritis: analysis of the PRINTO methotrexate trial. Ann Rheum Dis. 2010;69:1479–83. doi:10.1136/ard.2009.120840.
Albarouni M, Becker I, Horneff G. Predictors of response to methotrexate in juvenile idiopathic arthritis. Pediatr Rheumatol Online J. 2014;12:35. doi:10.1186/1546-0096-12-35.
Ravelli A, DI Fuccia G, Molinaro M, Ramenghi B, Zonta L, Regazzi MB, et al. Plasma levels after oral methotrexate in children with juvenile rheumatoid arthritis. J Rheumatol. 1993;20(9):1573–7.
Becker ML, Vhl, Gaedigk R, Lasky A, Hoeltzel MF, Stobaugh J, et al. Analysis of intracellular methotrexate polyglutamates in juvenile idiopathic arthritis: effect of route of administration upon intracellular methotrexate polyglutamate variability. Arthritis Rheum. 2010;62(6):1803–12.
Chabner BA, Allegra CJ, Curt GA, Clendeninn NJ, Baram J, Koizumi S, et al. Polyglutamation of methotrexate. Is methotrexate a prodrug? J Clin Invest. 1985;76(3):907–12.
Becker ML, Van Haandel L, Gaedigk R, Thomas B, Hoeltzel MF, Lasky A, et al. Red blood cell folate concentrations and polyglutamate distribution in juvenile arthritis: predictors of folate variability. Pharmacogenet Genomics. 2012;22(4):236–46.
Tukova J, Chladek J, Nemcova D, Chladkova J, Dolezalova P. Methotrexate bioavailability after oral and subcutaneous administration in children with juvenile idiopathic arthritis. Clin Exp Rheumatol. 2009;27:1047–53.
Balis FM, Mirro Jr J, Reaman GH, Evans WE, McCully C, Doherty KM, et al. Pharmacokinetics of subcutaneous methotrexate. J Clin Onkol. 1988;6:1882–6.
Albertioni F, Flatø B, Seideman P, Beck O, Vinje O, Peterson C, et al. Methotrexate in juvenile rheumatoid arthritis. Evidence of age dependent pharmacokinetics. J Clin Pharmacol. 1995;47(6):507–11.
Chladek J, Martinkova J, Simkova M, Vaneckova J. Pharmacokinetics of low doses of methotrexate in patients with psoriasis over the early period of treatment. Eur J Clin Pharmacol. 1998;53:437–44.
Hillson JL, Furst DE. Pharmacology and pharmacokinetics of methotrexate in rheumatic disease. Rheum Dis Clin North Am. 1997;23:757–78.
Chladek J, Grim J, Martinkova J, Simkova M, Vaneckova J. Low-dose methotrexate pharmacokinetics and pharmacodynamics in the therapy of severe psoriasis. Basic Clin Pharmacol Toxicol. 2005;96:247–8.
Becker ML, Rose CD, Cron RQ, Sherry DD, Bilker WB, Lautenbach E. Effectiveness and toxicity of methotrexate in juvenile idiopathic arthritis: comparison of two initial dosing regimens. J Rheumatol. 2010;37(4):870–5.
Kocharla L, Taylor J, Weiler J, Wiler T, Ting TV, Luggen M, et al. Monitoring Methotrexate Toxicity in Juvenile Idiopathic Arthritis. J Rheumatol. 2009;36(12):2813–8.
Ruperto N, Murray KJ, Gerloni V, Wulffraat N, de Oliveira SK, Falcini F, et al. Pediatric Rheumatology International Trials Organization a randomized trial of parenteral methotrexate comparing an intermediate dose with higher dose in children with juvenile idiopathic arthritis who failed to respond to standard doses of methotrexate. Arthritis Rheum. 2004;50(7):2191–201.
Bulatovič M, Heijstek MW, Verkaaik M, van Dijkhuizen EH, Armbrust W, Hoppenreijs EP, et al. High Prevalence of Methotrexate Intolerance in Juvenile Idiopathic Arthritis Development and Validation of a Methotrexate Intolerance Severity Score. Arthritis Rheum. 2011;63(7):2007–13. doi:10.1002/art.30367.
Roscoe JA, Morrow GA, Aapro MS, Molassiotis A, Olver I. Anticipatory nausea and vomiting. Support Care Cancer. 2011;19(10):1533–8.
van Dijkhuizen EH, Bulatović Ćalasan M, Pluijm SM, de Rotte MC, Vastert SJ, Kamphuis S, et al. Prediction of methotrexate intolerance in juvenile idiopathic arthritis: a prospective, observational cohort study. Pediatr Rheumatol Online J. 2015;13:5. doi:10.1186/s12969-015-0002-3.
van Dijkhuizen P, Pouw J, Scheuern A, Hügle B, Hardt S, Ganser G, et al. Intolerance in oral versus subcutaneous administration of methotrexate in patients with juvenile idiopathic arthritis: a cross-sectional, observational study. Pediatr Rheumatol Online J. 2014;12 Suppl 1:P131. doi:10.1186/1546-0096-12-S1-P131.
Petty RE, Southwood TR, Manners P, Baum J, Glass DN, Goldenberg J, et al. International league of associations for Rheumatology classification of juvenile idiopathic arthritis: 2nd revision, Edmonton, 2001. J Rheumatol. 2004;2:390–2.
Consolaro A, Ruperto N, Bracciolini G, Frisina A, Gallo MC, Pistorio A, et al. Defining criteria for high disease activity in juvenile idiopathic arthritis based on the Juvenile Arthritis Disease Activity Score. Ann Rheum Dis. 2014;73(7):1380–3.
Consolaro A, Bracciolini G, Ruperto N, Pistorio A, Magni-Manzoni S, Malattia C, et al. Remission, minimal disease activity, and acceptable symptom state in juvenile idiopathic arthritis: Defining criteria based on the juvenile arthritis disease activity score. Arthritis Rheumat. 2012;64(7):2366–74. doi:10.1002/art.34373.
Nordal EB, Zak M, Aalto K, Berntson L, Fasth A, Herlin T, et al. Validity and predictive ability of the juvenile arthritis desease activity score based on CRP versus ESR in a Nordic population-based setting. Ann Rheum Dis. 2012;71:1122–7.
McErlane F, Beresford MW, Baildam EM, Chieng EA, Davidson JE, Foster HE, et al. Validity of a three-variable Juvenile Arthritis Disease Activity Score in children with new-onset juvenile idiopathic arthritis. Ann Rheum Dis. 2013;72(12):1983–8. doi:10.1136/annrheumdis-2012-202031.
Wallace CA, Giannini EH, Huang B, Itert L, Ruperto N. Childhood Arthritis Rheumatology Research Alliance; Pediatric Rheumatology Collaborative Study Group; Paediatric Rheumatology International Trials Organisation. American College of Rheumatology provisional criteria for defining clinical inactive disease in select categories of juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2011;63(7):929–36. doi:10.1002/acr.20497.
Lurati A, Salmaso A, Gerloni V, Gattinara M, Fantini F. Accuracy of Wallace criteria for clinical remission in juvenile idiopathic arthritis: a cohort study of 761 consecutive cases. J Rheumatol. 2009;36(7):1532–5. doi:10.3899/jrheum.080434.
Ravelli A, Martini A. Remission in juvenile idiopathic arthritis. Clin Exp Rheumatol. 2006;24 Suppl 43:S105–10.
Wallace CA, Giannini EH, Spalding SJ, Hashkes PJ, O'Neil KM, Zeft AS, et al. Trial of early aggressive therapy in polyarticular juvenile idiopathic arthritis. Arthritis Rheum. 2012;64(6):2012–21.
Consolaro A, Calandra S, Robbiano C, Ravelli A. Treating Juvenile Idiopathic Arthritis According to JADAS-Based Targets. Ann Paediatr Rheum. 2014;3(1):4–10. doi:10.5455/apr.031720141940.
Ravelli A, Gerloni V, Corona F, Falcini F, Lepore L, De Sanctis R, et al. Oral versus intramuscular methotrexate in juvenile chronic arthritis. Clin Exp Rheumatol. 1998;16:181–3.
Alsufyani K, Ortiz-Alvarez O, Cabral DA, Tucker LB, Petty RE, Malleson PN. The role of subcutaneous administration of methotrexate in children with juvenile idiopathic arthritis who have failed oral methotrexate. J Rheumatol. 2004;31(1):179–82.
Klein A, Kaul I, Foeldvari I, Ganser G, Urban A, Horneff G. Efficacy and safety of oral and parenteral methotrexate therapy in children with juvenile idiopathic arthritis: an observational study with patients from the German Methotrexate Registry. Arthritis Care Res (Hoboken). 2012;64(9):1349–56. doi:10.1002/acr.21697.
Moncrieffe H, Ursu S, Holzinger D, Patrick F, Kassoumeri L, Wade A, et al. A subgroup of juvenile idiopathic arthritis patients who respond well to methotrexate are identified by the serum biomarker MRP8/14 protein. Rheumatology (Oxford). 2013;52(8):1467–76. doi:10.1093/rheumatology/ket152.
Bulatović Ćalasan M, den Boer E, de Rotte MC, Vastert SJ, Kamphuis S, de Jonge R, et al. Methotrexate polyglutamates in erythrocytes are associated with lower disease activity in juvenile idiopathic arthritis patients. Ann Rheum Dis. 2015;74:402–7. doi:10.1136/annrheumdis-2013-203723.
Pastore S, Stocco G, Favretto D, De Iudicibus S, Taddio A, d’Adamo P, et al. Genetic determinants for methotrexate response in juvenile idiopathic arthritis. Front Pharmacol. 2015;6:52. doi:10.3389/fphar.2015.00052.
Hinks A, Moncrieffe H, Martin P, Ursu S, Lal S, Kassoumeri L, et al. Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. Ann Rheum Dis. 2011;70:1395–400. doi:10.1136/ard.2010.146191.
de Rotte MC, Bulatovic M, Heijstek MW, Jansen G, Heil SG, van Schaik RH, et al. ABCB1 and ABCC3 gene polymorphisms are associated with first-year response to methotrexate in juvenile idiopathic arthritis. J Rheumatol. 2012;39(10):2032–40. doi:10.3899/jrheum.111593.
van der Meer A, Wulffraat NM, Prakken BJ, Gijsbers B, Rademaker CM, Sinnema G. Psychological side effects of MTX treatment in juvenile idiopathic arthritis: a pilot study. Clin Exp Rheumatol. 2007;25(3):480–5.
Figueroa-Moseley C, Jean-Pierre P, Roscoe JA, Ryan JL, Kohli S, Palesh OG, et al. Behavioral interventions in treating anticipatory nausea and vomiting. J Natl Compr Canc Netw. 2007;5:44–50.
Verkaaik M, Bulatović M, Sinnema G, Rademaker C, Wulffraat NM. Treatment of methotrexate (MTX) intolerance: behavioural therapy, versus switch to parenteral MTX versus oral MTX. Pediatr Rheumatol Online J. 2011;9 Suppl 1:O23. doi:10.1186/1546-0096-9-S1-O23.
Becker ML, Rosé CD, Cron RQ, Sherry DD, Bilker WB, Lautenbach E. Effectiveness and Toxicity of Methotrexate in Juvenile Idiopathic Arthritis: Comparison of 2 Inicial Dosing Regimens. Rheumatol. 2010;37(4):870–5. doi:10.3899/jrheum.090826.
Ortiz-Alvarez O, Morishita K, Avery G, Green J, Petty RE, Tucker LB, et al. Guidelines for blood test monitoring of methotrexate toxicity in juvenile idiopathic arthritis. J Rheumatol. 2004;31(12):2501–6.
Bartoli M, Tarò M, Magni-Manzoni S, Pistorio A, Traverso F, Viola S, et al. The magnitude of early response to methotrexate therapy predicts long-term outcome of patients with juvenile idiopathic arthritis. Ann Rheum Dis. 2008;67:370–4. doi:10.1136/ard.2007.073445.
Tynjälä P, Vähäsalo P, Tarkiainen M, Kröger L, Aalto K, et al. Aggressive Combination Drug Therapy in Very Early Polyarticular Juvenile Idiopathic Arthritis (ACUTE–JIA): a multicentre randomised open-label clinical trial. Ann Rheum Dis. 2011;70:1605–12. doi:10.1136/ard.2010.143347.
This study was supported by the grant from the Ministry of Health of the Czech Republic NT14149-3/2013
Availability of data and materials
We have not developed any new software or assessment tools. The instruments used are widely available and their resources have been appropriately cited. The patient data were entered in the excell spread sheets including their identification as only investigator team had an access to them. Patients have not consented on presenting their full data to any third parties.
The study was a part of the large departmental, investigator-initiated research project supported by the grant from the Ministry of Health of the Czech Republic number NT14149-3/2013.
JF participated in patient recruitment and follow-up assessments and in data analysis and drafted the manuscript. ŠF, KK and RS took part in patient recruitment and follow-up assessments and in data analysis. DN and JH participated in the study design, patient recruitment and follow-up assessments. MU participated in the study design and performed the statistical analysis. MS and LL participated in the study design and its co-ordination and were responsible for the quality of patient-reported outcome data. PD designed and co-ordinated the study, participated in patient recruitment and follow-up assessments and in data analysis and co-drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Fráňová, J., Fingerhutová, Š., Kobrová, K. et al. Methotrexate efficacy, but not its intolerance, is associated with the dose and route of administration. Pediatr Rheumatol 14, 36 (2016) doi:10.1186/s12969-016-0099-z
- Juvenile idiopathic arthritis
- Quality of life