- Open Access
A multicentre, efficacy and safety study of methotrexate to increase response rates in patients with uncontrolled gout receiving pegloticase (MIRROR): 12-month efficacy, safety, immunogenicity, and pharmacokinetic findings during long-term extension of an open-label study
Arthritis Research & Therapy volume 24, Article number: 208 (2022)
Publications suggest immunomodulation co-therapy improves responder rates in uncontrolled/refractory gout patients undergoing pegloticase treatment. The MIRROR open-label trial showed a 6-month pegloticase + methotrexate co-therapy responder rate of 79%, compared to an established 42% pegloticase monotherapy responder rate. Longer-term efficacy/safety data are presented here.
Uncontrolled gout patients (serum urate [SU] ≥ 6 mg/dL and SU ≥ 6 mg/dL despite urate-lowering therapy [ULT], ULT intolerance, or functionally-limiting tophi) were included. Patients with immunocompromised status, G6PD deficiency, severe kidney disease, or methotrexate contraindication were excluded. Oral methotrexate (15 mg/week) and folic acid (1 mg/day) were administered 4 weeks before and during pegloticase therapy. Twelve-month responder rate (SU < 6 mg/dL for ≥ 80% during month 12), 52-week change from baseline in SU, and extended safety were examined. Efficacy analyses were performed for patients receiving ≥ 1 pegloticase infusion. Pharmacokinetics (PK)/anti-drug antibodies (ADAs) were examined and related to efficacy/safety findings.
Fourteen patients were included (all male, 49.3 ± 8.7 years, 13.8 ± 7.4-year gout history, pre-therapy SU 9.2 ± 2.5 mg/dL). Three patients were non-responders and discontinued study treatment before 24 weeks, one patient exited the study per protocol at 24 weeks (enrolled prior to treatment extension amendment), and 10 remained in the study through week 52. Of the 10, 8 completed 52 weeks of pegloticase + methotrexate and were 12-month responders. The remaining two discontinued pegloticase + methotrexate at week 24 (met treatment goals) and stayed in the study under observation (allopurinol prescribed at physicians’ discretion); one remained a responder at 12 months. At 52 weeks, change from baseline in SU was − 8.2 ± 4.1 mg/dL (SU 1.1 ± 2.4 mg/dL, n = 10). Gout flares were common early in treatment but progressively decreased while on therapy (weeks 1–12, 13/14 [92.9%]; weeks 36–52, 2/8 [25.0%]). One patient recovered from sepsis (serious AE). Two non-responders developed high ADA titers; fewer patients had trough concentrations (Cmin) below the quantitation limit (BQL), and the median Cmin was higher (1.03 µg/mL vs. BQL) than pegloticase monotherapy trials.
Pegloticase + methotrexate co-therapy was well-tolerated over 12 months, with sustained SU lowering, progressive gout flare reduction, and no new safety concerns. Antibody/PK findings suggest methotrexate attenuates ADA formation, coincident with higher treatment response rates.
ClinicalTrials.gov, NCT03635957. Registered on 17 August 2018.
Gout is a common, inflammatory arthritis caused by monosodium urate deposition in the setting of chronically elevated serum urate levels (SU > 6 mg/dL). Monosodium urate crystals cause chronic systemic inflammation, even between acute gout flares [1, 2]. Additionally, hyperuricemia has been linked to multiple comorbidities, including hypertension [3, 4], cardiovascular disease [5,6,7,8,9], diabetes [3, 10], kidney disease [11, 12], metabolic syndrome , and a higher mortality rate [9, 14, 15]. Gout treatment guidelines recommend maintaining SU below at least 6 mg/dL [16, 17], but some patients are unable to meet this target because of urate-lowering therapy (ULT) under-utilization , patient non-compliance [19, 20], ULT intolerance, or ULT inefficacy . As a result, an estimated 10% of patients may develop uncontrolled gout , which markedly impairs patient quality of life and physical functioning .
Pegloticase, a pegylated uricase enzyme, is an FDA-approved therapy for adult patients with uncontrolled gout and is highly effective in lowering SU . It should be noted that pegloticase is commercially available only in the USA. The recombinant enzyme rapidly lowers SU by converting uric acid to allantoin, a water-soluble molecule that is readily excreted by the kidneys. Though the initial response to treatment is robust, many patients develop anti-drug antibodies (ADAs) to the therapy and are unable to complete a full course of treatment. Clinical trials of pegloticase monotherapy found a 42% treatment responder rate (responder defined as a patient with SU < 6.0 mg/dL for 80% of the time or longer during both months 3 and 6 of therapy), with approximately one-quarter (26%) of patients experiencing infusion reactions (IRs) when a pre-infusion monitoring protocol for SU was not followed [24, 25]. Anti-pegloticase antibodies that develop following pegloticase exposure are associated with both loss of urate-lowering effect, through increased pegloticase clearance, and a higher risk of IRs [26,27,28]. Starting in 2017, successes with immunomodulation co-therapy have been reported in the real-world setting with methotrexate [29, 30] and leflunomide  and in a clinical trial setting with azathioprine (TRIPLE open-label) , methotrexate (MIRROR open-label trial) , and mycophenolate mofetil in a randomized placebo-controlled clinical trial (RECIPE trial) . Likely related to these reports, immunomodulation use with pegloticase is increasing in the USA . In 2015, approximately 2% of patients treated with pegloticase were also treated with immunomodulation, whereas in 2019, 15% of new pegloticase patients were also treated with immunomodulating co-therapy . The initial MIRROR open-label clinical trial reports describe 6-month outcomes , but longer-term safety and efficacy have not yet been published. Here, 12-month efficacy outcomes are described, along with pharmacokinetic (PK) and immunogenicity findings.
This study population has been fully described elsewhere . Briefly, patients with uncontrolled gout aged 18 − 65 years were considered for trial enrollment. Patients were said to have uncontrolled gout if their SU level was ≥ 6 mg/dL at screening and at least one of the following was true: they were unable to maintain SU < 6 mg/dL on an oral ULT, they had an intolerance to their current ULT, or tophaceous deposits that limited patient functionality were present (detected clinically or with dual-energy computed tomography [DECT]). The key exclusion criteria included serious acute bacterial infection < 2 weeks prior to screening, severe chronic/recurrent bacterial infection, immunocompromised status, glucose-6-phosphate dehydrogenase (G6PD) deficiency (tested at screening), severe chronic renal impairment (glomerular filtration rate [GFR] < 25 mL/min/1.73 m2 or currently on dialysis), or liver disease (alanine aminotransferase [ALT] or aspartate aminotransferase [AST] > 3 times upper limit).
All enrolled patients were scheduled to receive 4 weeks of oral methotrexate (15 mg/week, run-in period) followed by treatment with both pegloticase (8 mg infusion every 2 weeks) and methotrexate (15 mg orally every week) for up to 52 weeks (treatment period). As previously described in this study’s first publication reporting 6-month findings , the methotrexate dose was chosen based on the enhancement of other biologics’ durability when methotrexate was used as co-therapy, published rheumatology expert opinions, and study advisory board recommendations. The original protocol included a 24-week treatment period, but a protocol amendment extended the treatment period to 52 weeks. Patients also received 1 mg/day of oral folic acid during both the run-in and treatment periods. All patients were required to begin gout flare prophylaxis (colchicine, non-steroidal anti-inflammatory drugs [NSAIDs], and/or low-dose prednisone [≤ 10 mg/day] as chosen by the treating physician) at least 1 week prior to initiating pegloticase, continuing flare prophylaxis per American College of Rheumatology guidelines . When they did occur, flares were managed with NSAIDs, colchicine, corticosteroids, and intraarticular steroid injections at the treating physician’s discretion.
Patients were administered standard IR prophylaxis prior to each pegloticase infusion. This included oral fexofenadine (60 or 180 mg) the day before and morning of infusion, acetaminophen (1000 mg) the morning of infusion, and intravenous glucocorticoid (200 mg hydrocortisone or 125 mg methylprednisolone) immediately prior to each infusion. An SU monitoring protocol  was implemented to decrease the risk of IRs. Patients discontinued pegloticase + methotrexate co-therapy if they had two consecutive SU measurements above 6 mg/dL after week 2.
Study procedures from screening to month 6 have been previously described . Briefly, screening included study eligibility confirmation and patient medical and surgical history (including concomitant medications), physical examination, gout assessment (including flare history), and laboratory testing (SU measurement, hematology, clinical chemistry). After eligibility was confirmed, patients began the 4-week methotrexate run-in period (− 4 weeks) within 2 weeks of screening and returned for physical, laboratory, gout flare, and safety assessment at week − 2.
Pegloticase therapy was initiated on day 1 (methotrexate and folic acid continued during pegloticase treatment) and had a maximum duration of 52 weeks. Patients returned every 2 weeks for follow-up assessment (concomitant medication update, physical examination) and pegloticase infusion [see Additional file 1]. Safety assessments at each study visit included adverse event (AE) evaluation and blood/urine sampling for laboratory measurement and SU monitoring. The published Rheumatology Common Terminology Criteria for Adverse Events (CTCAE) grading system (1 = mild, 2 = moderate, 3 = severe, 4 = life-threatening) was used to determine AE severity . When gout flares were documented, severity was assessed using a standardized flare grading system based on joint pain, joint swelling, and pain levels at rest .
Pharmacokinetics and anti-drug antibodies
Blood samples for pegloticase PK evaluations were collected before and after pegloticase infusion on day 1 and on weeks 4, 8, 22, and 36. Samples were also collected before pegloticase infusion at weeks 10, 14, 18, 22, and 52. Pre-infusion blood samples were collected from all patients to evaluate the immunogenicity of pegloticase by measuring both anti-PEG and anti-uricase immunoglobulin G (IgG) antibodies (ADAs) at day 1 and weeks 2, 4, 6, 8, 10, 14, 18, 22, 24, 36, and 52. A small subset of patients had additional visits at weeks 1 and 7 (non-infusion visits), during which blood samples were collected for both PK and antibody evaluations. Pre-infusion blood samples were also collected to measure methotrexate polyglutamate(s) (MTX-PGs 1 to 5) in red blood cells at day 1 and weeks 4, 8, 22, 24, and 36.
Pegloticase concentration in the serum was measured using a validated enzymatic/fluorescence assay (Charles River Laboratories, Senneville, Quebec, Canada). The calibration range was 0.6 to 10 µg/mL. ADAs were measured using a validated enzyme-linked immunosorbent assay (anti-pegloticase/PEG, anti-uricase; Precision for Medicine, Redwood City, CA, USA). The drug tolerance level was < 0.02 µg/mL in neat serum. Measurements of MTX-PG1 to 5 red blood cell concentrations were performed by Exagen Inc. (AVISE® MTX test; Vista, CA, USA) using a liquid chromatography–mass spectrometry method .
Pegloticase pharmacokinetic analysis
Serum pegloticase concentration data were analyzed using two methods to evaluate the impact of methotrexate co-therapy on pegloticase PK. First, pegloticase exposures (median observed peak concentration [Cmax] and trough concentration [Cmin] across visits) with methotrexate from the current study were compared to the observed values in historical monotherapy phase 3 studies (C0405 and C0406) [23, 26]. Second, the observed pegloticase concentrations with methotrexate co-therapy in the current study were overlaid against the 90% prediction band of pegloticase concentrations following monotherapy based on the population PK model from the phase 3 data . Pharmacokinetic profiles of pegloticase following 8 mg IV infusion every 2 weeks for a total of 12 infusions were simulated for 400 patients with an average body surface area of 2.12 m2 (percent coefficient of variation = 13.3%). The population PK simulations were done using NONMEM 7.4 (ICON Development Solutions, Ellicott City, MD, USA).
The primary efficacy endpoint was the proportion of responders during month 6 (SU < 6 mg/dL for ≥ 80% of month 6) and has been fully reported elsewhere . Secondary and exploratory efficacy objectives described here include the proportion of treatment responders (SU < 6 mg/dL during ≥ 80% of the examined time) during months 3, 9, and 12; overall response rate during months 3 and 6 combined; and mean change from baseline in SU at weeks 14, 24, 36, and 52. A sample size of 12–16 patients was planned, which would demonstrate a statistically greater response rate over pegloticase monotherapy if at least 10/13 (77%) patients were responders for the primary endpoint (proportion of pegloticase responders during month 6 in pegloticase pivotal trials [43.5%] ), based on an exact test for proportions with a 5% type 1 error. Longer-term (9 months, 12 months) efficacy endpoints do not have established historical comparators.
All efficacy and safety analyses were performed on the modified intent-to-treat (mITT) population, defined as all patients who received at least 1 dose of pegloticase. Continuous variables are summarized by visit as mean ± standard deviation, and categorical variables are summarized as n (%). SU values below quantification limits (BQL) were set to zero for analyses. Safety analyses were also performed on data collected during the run-in period using the ITT population, defined as all patients who received at least 1 dose of methotrexate. The incidence and titer of positive ADAs (anti-PEG and anti-uricase) are summarized by visit.
Seventeen patients were screened for study eligibility between September 2018 and April 2019. Fifteen patients began the methotrexate run-in period and made up the ITT population. Fourteen completed the entire 4-week run-in period (1 patient was lost to follow-up after week − 2), began pegloticase + methotrexate co-therapy, and made up the mITT population through week 24. As already reported, 11 of 14 completed 24 weeks of pegloticase + methotrexate co-therapy for a 6-month responder rate of 79% (95% CI 49.2 to 95.3%; 3 patients discontinued pegloticase prior to 24 weeks because of SU rise) . Of the 11 patients remaining in the study at week 24, 8 continued therapy through week 52, 2 met gout treatment goals (as determined by the treating investigator) at week 24 discontinuing study treatment but remaining in the study for observation through week 52, and 1 completed the study at week 24 (enrolled prior to protocol amendment that extended treatment). One of the patients who met the treatment goals at week 24 initiated allopurinol at the treating investigator’s discretion at week 24 (300 mg/day for 1 week, 600 mg/day for 2 weeks, then 300 mg/day through week 52), and the other patient started allopurinol at week 26 (150 mg/day for 21 weeks then 300 mg/day through week 52 [see Additional file 2]). The patient who completed the study at week 24 was not included in the analyses beyond 24 weeks (i.e., mITT N = 13 after week 24).
Table 1 summarizes the mITT patient characteristics at baseline. Briefly, patients were 49.3 ± 8.7 years of age and had an average gout history of 13.8 ± 7.4 years. Prior to initiating pegloticase, SU averaged 9.2 ± 2.5 mg/dL and 13 patients (93%) had clinically evident tophi.
All 8 patients who continued pegloticase + methotrexate co-therapy through week 52 were treatment responders during months 9 and 12. Pegloticase response rate in the mITT population was 10 of 13 patients (76.9%) during month 9 and 9 of 13 patients (69.2%) during month 12 (Table 2). Of the 4 patients who did not meet the response criteria during month 12, all had discontinued study treatment prior to (3 patients met the pegloticase discontinuation criteria [1 patient each at week 4, week 6, and week 10]) or at week 24 (1 patient met the treatment goals and discontinued pegloticase). After initiating pegloticase, SU rapidly decreased and was 0.0 ± 0.0 mg/dL at week 24 (change from baseline − 9.3 ± 2.8 mg/dL, n = 11) and 1.1 ± 2.5 mg/dL at week 52 (change from baseline − 8.2 ± 4.1 mg/dL, n = 10). In the patients remaining on pegloticase + methotrexate treatment through week 52 (n = 8), SU was 0.0 ± 0.0 at weeks 36 and 52 (change from baseline − 9.4 ± 3.3 mg/dL; Fig. 1, Table 2). In the 2 patients who remained in the study, but discontinued pegloticase + methotrexate at week 24, SU remained < 6 mg/dL until week 36 in the patient who initiated allopurinol at week 24 and until week 50 in the patient who initiated allopurinol at week 26 [see Additional file 2].
The measured concentrations of MTX-PGs were maintained during the treatment course, suggesting compliance with MTX administration [see Additional file 3]. Concomitant treatment with methotrexate generally improved pegloticase exposures, resulting in a lower proportion of patients with Cmin BQL on methotrexate (5/14 [36%] vs. without methotrexate 63/82 [77%]) and higher overall Cmin (median [Q1, Q3] 1.03 (BQL, 1.23) µg/mL with methotrexate vs. BQL [BQL, BQL] without methotrexate), as well as slightly higher peak concentration Cmax (median [Q1, Q3] 2.11 [1.65, 2.59] µg/mL with methotrexate vs. 1.51 [BQL, 2.48] µg/mL without methotrexate; Fig. 2, Table 3). Consistently, pegloticase + methotrexate co-treatment resulted in more observed pegloticase concentrations above the predicted median value of pegloticase monotherapy (66% for the entire 14-day dosing interval and 82% for trough concentrations, Fig. 3). All non-responders had pegloticase Cmin BQL across time points, whereas responders typically had measurable Cmin values across most time points with the exception of two patients that only have Cmin above BQL for a few visits (Fig. 2).
ADA data are consistent with the improved pegloticase efficacy and PK when co-administered with methotrexate. An increase in ADA titer was observed in 2 of 3 non-responders (1 patient from < 10 at baseline to 320 at week 4, 1 patient 40 at baseline to 640 at week 2) and temporally corresponded with the loss of pegloticase exposure and SU increase. The third non-responder received 5 pegloticase infusions prior to meeting the SU discontinuation criteria. This patient was positive for anti-PEG antibody titer prior to the first pegloticase dose but negative during the treatment period. Two of eleven responders at month 6 showed a small increase (≤ 40) in anti-PEG antibody titer at a single time during pegloticase + methotrexate treatment. All other anti-PEG antibody titer measurements were either negative or no greater than the baseline levels. The remaining 9 responders were considered negative for the induction of anti-PEG antibodies.
Ten patients (66.7%) experienced an AE during the run-in period, including gout flare (5 patients), nausea (2 patients), and abdominal discomfort (2 patients, Table 4). All patients experienced one or more AEs during pegloticase + methotrexate Treatment, most commonly gout flare (13 patients [92.9%]). Patients also experienced diarrhea, nasopharyngitis, upper respiratory tract infection, muscle strain, and arthralgia (3 patients each [21.4%], Table 4). One SAE of bacterial sepsis secondary to cholecystitis was observed and deemed unrelated to the study treatments by the reporting investigator.
Infusion reaction, anaphylaxis, cardiovascular events, and gout flare were AEs of special interest. A single IR was reported in one patient following the 5th pegloticase infusion (week 8 visit). As previously detailed , the event was described by the investigator as a mild cough that began towards the end of the infusion and resolved without treatment after approximately 1 h. Typical IR signs (hives, itching, shortness of breath, sweating, chills) were not present. In this patient, SU remained BQL, and the patient met the responder criteria during month 6 (exited study at week 24). Anaphylaxis, cardiovascular event, and major adverse cardiovascular event (including non-fatal myocardial infarction, non-fatal stroke, cardiovascular death, and congestive heart failure) were not observed during any study period. Thirteen patients (92.9%) experienced gout flares during treatment (2 severe flares). However, both the number of patients on treatment who flared and the frequency of flares decreased over time, from 4.2 ± 2.3 flares (range 1–8 flares) in 13 of 14 patients (92.9%) during the initial 12 weeks of treatment to 2.5 ± 0.7 flares (range 2–3 flares) in 2 of 8 patients (25.0%) during weeks 37–52 (Fig. 4).
Liver and kidney functions were carefully monitored during both the run-in and treatment periods. At screening, 3 patients in the mITT population (21.4%) had an ALT above the upper limit of normal (ULN), and 2 patients (14.3%) had an AST above the ULN. A minor, transient increase in LFTs occurred shortly after methotrexate initiation, with LFTs stabilizing below the ULN at week 2 (Fig. 5a, b). LFTs remained stable through week 52. Two patients experienced one mild (grade 1) LFT elevation, both of which resolved following a methotrexate dose reduction (15 to 10 mg/week at week 25 in 1 patient [titrated back to 15 mg/week beginning at week 37] and week 2 in 1 patient). Methotrexate was otherwise well-tolerated in the mITT population. One patient had an accidental dose reduction to 12.5 mg/week on 2 occasions (weeks 9 and 18). All 3 patients who had a methotrexate dose reduction remained treatment responders during the pegloticase + methotrexate treatment period.
The mean estimated glomerular filtration rate (eGFR) was 84.6 ± 21.7 mL/min/1.73 m2 just prior to beginning methotrexate (week − 4, n = 14) and remained stable throughout the methotrexate run-in and pegloticase + methotrexate treatment periods (Fig. 5c). The mean eGFR was 88.3 ± 21.1 mL/min/1.73 m2 at week 24 (change from week − 4, + 4.2 ± 14.9 mL/min/1.73 m2, n = 11) and 80.9 ± 22.4 mL/min/1.73 m2 at week 52 (change from week − 4, − 4.0 ± 18.3 mL/min/1.73 m2, n = 10).
Compared to previously reported responder rates for pegloticase monotherapy, an increased proportion of patients treated with methotrexate in conjunction with pegloticase maintained therapeutic response during month 6 (42% vs. 79% ). Furthermore, all 6-month responders who remained on pegloticase + methotrexate co-therapy continued to be treatment responders through month 12 (SU < 1 mg/dL in all 8 patients). The duration of treatment response to pegloticase is of vital importance to patients with uncontrolled gout, many of whom pegloticase is their last medical treatment option.
The increased pegloticase treatment response rate is almost certainly attributable to the addition of methotrexate. Pegloticase is highly effective in lowering SU, but many patients have an incomplete response due to developing ADAs targeting polyethylene glycol moieties resulting in increased pegloticase clearance [24, 27]. When compared to historical phase 3 pivotal trial data, PK and ADA data from the current trial suggest that methotrexate reduces the immunogenicity of pegloticase and prolongs the biologic activity of pegloticase. Similar findings have been previously observed with other biologics (e.g., infliximab , adalimumab [40, 41], and certolizumab pegol ). The median pegloticase Cmin was higher (1.03 μg/mL with methotrexate vs. BQL without methotrexate), and the proportion of patients with a pegloticase Cmin BQL (36% vs. 77%) was lower in patients treated with pegloticase + methotrexate co-therapy than those treated with pegloticase monotherapy (the lowest quantitation limit was similar between studies). Furthermore, 2 of 11 primary endpoint responders in the current trial developed low titer (≤ 40) anti-PEG antibodies at a single visit following pegloticase treatment (the remaining 9 responders were ADA-negative or did not exceed their baseline ADA levels). In contrast, 2 of the 3 non-responders developed ADA titers concomitantly with an undetectable serum pegloticase concentration and increase in SU above 6 mg/dL. The remaining non-responder was positive for anti-PEG antibody titer prior to the first pegloticase dose, but negative thereafter. Pre-infusion serum pegloticase concentration was undetectable throughout treatment for reasons that remain unclear. It is worth noting that the detection of antibody formation is dependent on assay sensitivity and specificity and that the incidence of antibody positivity may be influenced by assay processing methodology. Therefore, a comparison of antibody incidence in the current study to historical pegloticase studies may not be appropriate. Concentrations of MTX-PGs were maintained during the treatment course, suggesting compliance with methotrexate administration. Additionally, there was no apparent difference in MTX-PG concentrations between responders and non-responders (data not shown).
Extended safety data indicate that pegloticase + methotrexate co-therapy was well tolerated over the 52-week treatment period, and no new safety concerns over pegloticase monotherapy or the 6-month findings  were identified. Gout flares remained the most common AE observed (13 of 14 patients [92.9%]) and occurred in most patients during the first 12 weeks of pegloticase therapy. However, both the number of patients experiencing flares and the frequency of flares markedly decreased over time. On average, worsening of hepatic or renal function was not noted throughout the run-in or treatment periods. Two AEs of increased LFTs were observed. Both were graded as mild and resolved with methotrexate dose reduction. Other AEs that were observed in more than 1 patient during the treatment period included diarrhea, nasopharyngitis, upper respiratory tract infection, arthralgia, muscle strain, sinusitis, and hypertension.
This study was limited by its small size, open-label design, and lack of a control group. Larger, randomized, placebo-controlled trials are needed to more rigorously examine the benefits and associated risks of administering methotrexate in conjunction with pegloticase to patients with uncontrolled gout. Such a trial has recently been completed (MIRROR RCT, NCT03994731). Our study findings prompt several clinical questions that cannot be answered with these data. First, it is not unheard of for patients to be treated with pegloticase for longer than 12 months. However, this study did not examine the risks and benefits of pegloticase + methotrexate co-therapy past treatment month 12. Second, the question of when to re-initiate oral ULT following pegloticase discontinuation remains. Some physicians restart oral ULT immediately in tolerant patients, while others wait until SU rises above 6 mg/dL. Lastly, there remains the question if lower doses of methotrexate may be able to achieve similar successful results as those seen here. Further studies to answer all of these questions are needed.
In conclusion, these data further support the use of methotrexate with pegloticase in patients with uncontrolled gout. New pharmacokinetic and ADA data presented here strongly suggest that methotrexate reduces immunogenicity to pegloticase, allowing more patients to accomplish treatment goals from full courses of therapy with a reduction in previously seen adverse effects. This benefit seems to be sustained for at least 12 months in patients remaining on co-therapy with both pegloticase and methotrexate.
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Below quantification limits
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We acknowledge the following employees of Horizon Therapeutics: Lissa Padnick-Silver, Ph.D., and Megan Francis-Sedlak, Ph.D., for the writing and editorial assistance and Colleen Canavan, M.S., for the trial support. We also acknowledge Exagen, Inc. for assistance with performing and interpreting MTX-PG measurements.
This work was supported by Horizon Therapeutics plc. Horizon was involved in the study design and data collection, analysis, and interpretation. Horizon was also involved in manuscript drafting and editing.
Ethics approval and consent to participate
This multicentre, open-label, efficacy and safety study (ClinicalTrials.gov: NCT03635957) was reviewed and approved for the 6 participating sites by the Western Institutional Review Board (Puyallup, WA; IRB assurance number: IRB00000533, protocol approval number 20182156). All patients provided written informed consent to participate, and all study conduct adhered to the tenants of the Declaration of Helsinki.
Consent for publication
JKB has received research support from Horizon Therapeutics and Radius Health as a study site and principal investigator. He has received consulting/speaker fees > 10 k from Horizon Therapeutics, Celgene, Novartis, and AbbVie. JRPT has served as a consultant/advisory board member for BMS, Janssen, Lilly Pfizer, Sanofi-Genzyme, AbbVie, Aurinia, AstraZeneca, and Samumed/Biosplice. He has served as a speaker for AbbVie, Amgen, BMS, Janssen, Lilly, Pfizer, Sanofi/Genzyme, Aurinia, AstraZeneca, and GlaxoSmithKline. He has received research grants and support from AbbVie, Amgen, BMS, Boehringer Ingelheim, Genentech, Gilead, Horizon Therapeutics, Janssen, Lilly, Pfizer, Vorso, Samumed/Biosplice, Selecta, Exagen, CSL Behring, Organogenesis, SunPharma, DRL, and Emerald. RB declares that there are no competing interests. HMK has received research support from Horizon Therapeutics (study site/investigator), is an advisor and speaker for Horizon Therapeutics, and is an owner and chairman of the Board of Discus Analytics (JoinMan). KO, YS, BL, LZ, YX, and JC are employees of and own stock in Horizon Therapeutics. PMP and SR were employees of Horizon Therapeutics during the study and own stock in Horizon. MEW has received grants from Amgen, Bristol-Myers Squibb, Lilly, and Sanofi. He has received consulting fees greater than US $10,000 from Chemocentryx, Corona, and Genosco and less than US $10,000 from AbbVie, Amgen, Aclaris, Arena, Bayer, Bristol Meyer Squibb, Crescendo Myriad Genetics, GlaxoSmithKline, Gilead Sciences, Horizon Therapeutics, Johnson and Johnson, Eli Lilly, Novartis, Pfizer, Rani Therapeutics, Roche, Samsung, Scipher Medicine, Set Point, Tremeau, and XBiotech; he has stock options in Can-Fite BioPharma, Scipher Medicine, Inmedix, and Vorso and royalties from Elsevier as co-editor for the textbook Rheumatology. JP has received research support from Horizon Therapeutics (study site/investigator). He has also served as an advisor and speaker for Horizon Therapeutics.
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Additional file 1: Supplement Table 1a.
Schedule of assessments, screening through Week 24. Supplement Table 1b. Schedule of assessments, Weeks 26-52.
Additional file 2: Supplemental Figure 1.
Serum urate levels in the two patients treated with pegloticase+methotrexate co-therapy for 24 weeks. Both patients met pegloticase treatment goals and continued in study on observation. Allopurinol was started at the investigators’ discretion. One patient (Patient 1) initiated allopurinol at Week 24 (300 mg/day for 1 week [Week 25], 600 mg for 2 weeks [Week 27], 300 mg/day thru Week 52) and the other (Patient 2) initiated allopurinol 2 weeks after discontinuing pegloticase+methotrexate (150 mg/day until Week 47, 300 mg/day thru Week 52).
Additional file 3: Supplemental Figure 2.
Individual concentration-time course of pegloticase and MTX polyglutamates.
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Botson, J.K., Tesser, J.R.P., Bennett, R. et al. A multicentre, efficacy and safety study of methotrexate to increase response rates in patients with uncontrolled gout receiving pegloticase (MIRROR): 12-month efficacy, safety, immunogenicity, and pharmacokinetic findings during long-term extension of an open-label study. Arthritis Res Ther 24, 208 (2022). https://doi.org/10.1186/s13075-022-02865-z