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Predictors of abatacept retention over 2 years in patients with rheumatoid arthritis: results from the real-world ACTION study

  • Rieke AltenEmail author
  • Xavier Mariette
  • Hanns-Martin Lorenz
  • Hubert Nüßlein
  • Mauro Galeazzi
  • Federico Navarro
  • Melanie Chartier
  • Julia Heitzmann
  • Coralie Poncet
  • Christiane Rauch
  • Manuela Le Bars
Open Access
Original Article

Abstract

Objectives

Evaluate abatacept retention over 2 years in the AbataCepT In rOutiNe clinical practice (ACTION) study.

Method

ACTION was an international, observational study of patients with moderate-to-severe rheumatoid arthritis (RA) who initiated intravenous abatacept. Crude abatacept retention rates over 2 years were estimated using Kaplan–Meier analyses in biologic-naive and -failure patients. Clinically relevant risk factors and significant prognostic factors for retention were evaluated using a Cox proportional hazards multivariable model.

Results

Overall, 2350/2364 enrolled patients were evaluable; 673 (28.6%) were biologic naive and 1677 (71.4%) had prior biologic failure (1 biologic, 728/1677 [43.4%]; ≥ 2 biologics, 949/1677 [56.6%]). Abatacept retention rate (95% confidence interval [CI]) at 2 years was 47.9% (45.7, 50.0): 54.5% (50.4, 58.3) for biologic-naive vs 45.2% (42.7, 47.7) for biologic-failure patients (log-rank P < 0.001). For patients with 1 and ≥ 2 prior biologic failures, respectively, retention rates (95% CI) were 50.2% (46.3, 53.9) vs 41.3% (38.0, 44.6; log-rank P < 0.001). Main reasons for discontinuation (biologic-naive vs biologic-failure, respectively) were lack of efficacy (61.4 vs 67.7%) and safety (21.3 vs 21.2%). Rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) double positivity versus negativity were predictive of higher retention in both biologic-naive (hazard ratio [HR] [95% CI] 0.71 [0.53, 0.96]; P = 0.019) and biologic-failure patients (HR [95% CI] 0.76 [0.62, 0.94]; P = 0.035).

Conclusions

Abatacept initiation as earlier vs later line of therapy in RA may achieve higher 2-year retention rates. RF and anti-CCP seropositivity could predict increased abatacept retention, irrespective of treatment line.

Trial registration

NCT02109666

Keywords

Biologic Efficacy Predictor Remission Rheumatoid arthritis 

Introduction

Management of patients with rheumatoid arthritis (RA) has evolved in recent years to include more personalized, strategic use of the range of therapeutic agents now available [1, 2]. Recommendations have been developed with the aim of optimizing clinical outcomes in every patient with RA through a treat-to-target approach to achieve sustained disease remission or low disease activity (LDA) [2]. In the presence of poor prognostic factors, treatment progression from a conventional synthetic (cs) disease-modifying anti-rheumatic drug (DMARD) to the inclusion of a biologic (b) DMARD such as abatacept can have unpredictable benefit [3].

Randomized controlled trials have provided evidence of the efficacy, safety and tolerability of abatacept in adults with moderate-to-severe RA [4, 5, 6]. However, a high proportion of patients with RA are unlikely to meet the stringent criteria required for participation in trials of biologics and study participants may not fully represent a clinical population [7]. Real-world data can provide valuable insights into the long-term use of biologics and the patient characteristics associated with the diverse responses observed in clinical settings [8, 9]. The determination of predictors of treatment retention and differential response will assist the development of the most appropriate, individualized treatment and has the potential to reduce unnecessary adjustments in therapy.

Abatacept is approved for the treatment of adults with moderate-to-severe RA [10, 11] and, uniquely, exerts a therapeutic effect through interaction with immune cells involved in the pathophysiology of RA by selective modulation of the C28:CD80/CD86 co-stimulation signal that is necessary for full T cell activation [12]. AbataCepT In rOutiNe clinical practice (ACTION; ClinicalTrials.gov identifier: NCT02109666) was a 2-year study to provide prospective, real-world data on abatacept retention, efficacy, and safety in patients with RA. The primary objective was to evaluate the retention of abatacept prescribed to adults with RA in a routine clinical setting. Secondary objectives included the identification of predictors of abatacept retention. Here we report the final 2-year results for all patients enrolled in ACTION.

Patients and methods

Study design

ACTION was a 2-year, non-interventional, international, multicentre cohort study in patients with RA initiating intravenous (IV) abatacept in clinical practice. The study design has been reported previously [13]. Patients were enrolled across Europe (Austria, Belgium, Czech Republic, Denmark, France, Germany, Greece, Italy, Netherlands, Spain, and Switzerland) and Canada. All participating countries were required to have regulatory approval and a reimbursement policy for abatacept to ensure availability of the drug to all eligible patients.

Rheumatologists were randomly selected for a well-balanced geographic distribution and were representative of specialists caring for patients with RA in each participating country. No product was provided to the physicians or patients by the study sponsor, and the observational design of the study did not interfere with usual clinical practice.

The final 2-year results for all patients enrolled in ACTION between May 2008 and December 2013 are reported here.

Study population

Patients eligible for inclusion were adults (aged ≥ 18 years) with moderate-to-severe RA, as defined by the American College of Rheumatology revised criteria 1987 [14], who initiated IV abatacept under the guidance of their physician and in accordance with the Summary of Product Characteristics in Europe [10] or the Product Monograph in Canada [11]. Patients were enrolled in ACTION either prospectively on initiation of abatacept or retrospectively within 3 months of initiation where authorized by the local ethics committee. Patients were recruited over three time periods that reflected the regulatory approval of abatacept in the participating countries [2]: May 2008–December 2010 (patients who were biologic naive or had prior ≥ 1 biologic failure; cohort A); September 2010–December 2013 (biologic-naive patients only; cohort B); and October 2011–December 2013 (patients with ≥ 1 prior biologic failure only; cohort C). Patients already participating in a clinical trial were excluded from ACTION.

Patients were followed up approximately every 3 months for 30 months in accordance with routine clinical practice or, if abatacept was discontinued before the end of the study, for up to 6 months after discontinuation. The ACTION study database was locked on 22 July 2016.

The study protocol and patient enrolment materials were approved by local ethics committees and regulatory agencies in each participating country (first approval received on 31 January 2008, Munich, Germany). The study was conducted in accordance with the Declaration of Helsinki [15], the International Conference on Harmonization Good Clinical Practice Guidelines [16], and the Good Epidemiological Practice Guidelines [17]. All enrolled patients provided informed consent in accordance with local laws.

Study outcomes

The primary endpoint was crude abatacept retention rate over 2 years. Retention was defined as consecutive time on treatment. Biologic-failure patients were those in whom a previous biologic was ineffective or had caused safety or tolerability concerns, patients in clinical remission or in whom there was a major improvement of symptoms following a previous biologic, or patients who had discontinued a previous biologic for any reason [18]. The first date of abatacept discontinuation and the reasons for discontinuation were recorded by the physician at follow-up, irrespective of whether the patient subsequently switched to subcutaneous (SC) abatacept or resumed treatment with IV abatacept, Exposure to abatacept was defined as the time between the dates of the first and last infusion of abatacept, plus 30 days.

Clinical response to abatacept at 2 years was assessed using European League Against Rheumatism (EULAR) response rates based on the 28-joint Disease Activity Score (DAS28) (erythrocyte sedimentation rate [ESR] or C-reactive protein [CRP]) and classified as good/moderate or no response [19]. Other assessments included clinical remission defined by DAS28 (ESR or CRP; < 2.6), Clinical Disease Activity Index (CDAI; ≤ 2.8), Simplified Disease Activity Index (SDAI; ≤ 3.3), and Boolean criteria [20].

Potential predictors of abatacept retention, including demographics, disease characteristics, co-morbidities at abatacept initiation, and previous and current treatments at baseline, were assessed in biologic-naive patients and in patients with prior biologic failure. Between-country effects were explored in patients from countries that recruited more than 10 patients, with Germany (highest number of enrolments) as the reference country.

Safety was monitored and evaluated in accordance with local regulations. The drug manufacturer’s pharmacovigilance department was notified of any adverse events (AEs) or serious adverse events (SAEs) assessed by the treating physician as related to abatacept or any other Bristol-Myers Squibb drug. An SAE was defined as an AE that was fatal or life-threatening, required or extended hospitalization, led to persistent or significant disability or incapacity, induced a birth defect, or was considered an important medical event. Deaths from any cause were reported. Safety is presented for the overall population, irrespective of treatment line.

Statistical analyses

Baseline characteristics and demographics were reported using descriptive statistics including sample size, mean, median and standard deviation (SD) for continuous variables, and frequency and percentage for categorical variables, and were compared using Fisher’s exact tests. Crude abatacept retention rates over 2 years with corresponding 95% confidence intervals (CIs) were estimated using Kaplan–Meier analyses for patients stratified by previous biologic exposure (biologic naive, 1 previous biologic, and ≥ 2 previous biologics) and compared by treatment line using a log-rank test.

Clinical outcomes at 2 years were assessed in patients with relevant baseline data collected no later than 8 days after the first abatacept infusion and were compared by treatment line using Fisher’s exact tests.

Clinically relevant known risk factors and predictors of abatacept discontinuation with significance (P ≤ 0.20) in univariable analyses and no collinearity were entered into multivariable Cox proportional hazards regression models (as shown in Supplementary Table S1 [see Online Resource 1]). Factors with a significance of P ≤ 0.10 after backward selection were retained in the final multivariable models. Results are presented as hazard ratios (HRs) with corresponding 95% CIs and P values. The HRs were statistically significant when the 95% CIs did not cross 1.

Results

Patients

Between May 2008 and December 2013, 2364 patients were enrolled in ACTION across Europe and Canada (cohort A, 1137 patients from 9 countries; cohort B, 555 patients from 8 countries; cohort C, 672 patients from 8 countries; Supplementary Fig. S1 [see Online Resource 2]). A total of 2350 patients were evaluable; 673 (28.6%) were biologic naive and 1677 (71.4%) had failed biologic treatment (1 biologic, 728/1677 [43.4% patients]; ≥ 2 biologics, 949/1677 [56.6% patients]) (Fig. 1). One patient erroneously classified as biologic naive for the 1-year analysis of ACTION was reclassified as a biologic-failure patient for this analysis [18]. For biologic-failure patients, 816/1677 (48.7%) had failed 1 tumor necrosis factor inhibitor (TNFi) and 805/1677 (48.0%) had failed ≥ 2 TNFis; 56/1677 (3.3%) had failed a non-TNFi biologic only.
Fig. 1

Patient disposition

Overall, baseline demographics were similar in all patients irrespective of treatment line (Table 1); however, in those who were biologic naive vs those with previous biologic failure at abatacept initiation, a higher proportion of patients had mean disease duration of ≤ 2 years (35.7 vs 9.0%; P < 0.001), mean CRP was lower (1.7 vs 2.1 mg/dL; P = 0.01), and a smaller proportion of patients had radiographic erosions (58.2 vs 71.5%; P < 0.001). Hypertension was the most common co-morbidity overall (38.2% and 39.1% of biologic-naive and biologic-failure patients, respectively). At abatacept initiation, over 90% of all patients had received prior methotrexate (Table 1); however, a greater proportion of biologic-failure vs biologic-naive patients had previous exposure to > 3 csDMARDs (6.9 vs 1.2%; P < 0.001), initiated abatacept as monotherapy (25.5 vs 16.6%; P < 0.001), and initiated abatacept with corticosteroids at a dose of > 5 mg/day (54.9 vs 47.3%; P < 0.01). The bDMARDs most commonly used previously by biologic-failure patients were etanercept and adalimumab (60.2% and 57.7% patients, respectively; Table 1).
Table 1

Baseline patient characteristics

 

Biologic naive (n = 673)

Biologic failure (n = 1677)

Age, years

59.9 (12.7)

57.0 (12.5)

Female, n (%)

496 (73.7)

1379 (82.2)

BMI, kg/m2

27.0 (5.4); n = 644

27.1 (5.6); n = 1597

BMI, n (%)

 < 25 kg/m2

265 (41.1)

649 (40.6)

 25–< 30 kg/m2

224 (34.8)

543 (34.0)

 ≥ 30–< 35 kg/m2

104 (16.1)

266 (16.7)

 ≥ 35 kg/m2

51 (7.9)

139 (8.7)

RA duration, years

7.2 (8.2); n = 669

12.1 (9.1); n = 1669

RA duration, n (%)

 ≤ 2 years

239/669 (35.7)*

151/1669 (9.0)

 3–5 years

155/669 (23.2)

320/1669 (19.2)

 6–10 years

122/699 (18.2)

421/1669 (25.2)

 > 10 years

153/699 (22.9)

777/1669 (46.6)

TJC28

9.0 (6.5); n = 633

10.4 (7.2); n = 1599

SJC28

6.6 (5.0); n = 641

7.0 (5.6); n = 1607

DAS28 (ESR)a

5.3 (1.2); n = 582

5.5 (1.3); n = 1422

DAS28 (CRP)a

4.8 (1.1); n = 568

5.0 (1.1); n = 1411

CDAIa

27.5 (11.5); n = 565

30.0 (12.9); n = 1388

SDAIa

29.1 (12.0); n = 526

31.8 (13.6); n = 1279

HAQ-DI

1.4 (0.7); n = 579

1.5 (0.7); n = 1471

PtGA, 100 mm VAS

62.0 (20.3); n = 620

65.4 (19.9); n = 1539

CRP, mg/dL

1.7 (2.6); n = 590

2.1 (3.5); n = 1474**

ESR, mm/h

33.1 (23.7); n = 605

33.7 (23.7); n = 1491

RF positive, n/N (%)

415/578 (71.8)

987/1385 (71.3)

Anti-CCP positive, n/N (%)

368/556 (66.2)

884/1309 (67.5)

RF and anti-CCP antibody status, n/N (%)

 Double positive

311/513 (60.6)

717/1166 (61.5)

 Single positive

77/513 (15.0)

182/1166 (15.6)

 Double negative

125/513 (24.4)

267/1166 (22.9)

Radiographic erosion, n/N (%)

353/607 (58.2)

1034/1446 (71.5)*

≥ 1 Co-morbidity, n (%)

518 (77.0)

1226 (73.1)

 Diabetes mellitus

85 (12.6)

207 (12.3)

 COPD

69 (10.3)

128 (7.6)

 Cardiac disorders

62 (9.2)

124 (7.4)

 Neoplasmsb

36 (5.3)

42 (2.5)*

Number of previous csDMARDsc, n (%)

 ≤ 3

655 (98.8)

1561 (93.1)

 > 3

8 (1.2)

116 (6.9)*

Previous MTX, n (%)

621 (92.3)

1552 (92.5)

Previous other csDMARDs, n (%)

 Leflunomide

278 (41.3)

951 (56.7)*

 Hydroxychloroquine/chloroquine

229 (34.0)

681 (40.6)**

 Sulfasalazine

148 (22.0)

578 (34.5)*

Previous corticosteroids, n (%)

533 (79.2)

1386 (82.6)

Previous other biologics, n (%)

 Adalimumab

967 (57.7)

 Anakinra

69 (4.1)

 Canakinumab

1 (0.1)

 Certolizumab

52 (3.1)

 Etanercept

1010 (60.2)

 Golimumab

22 (1.3)

 Infliximab

512 (30.5)

 Ocrelizumab

3 (0.2)

 Rituximab

239 (14.3)

 Tocilizumab

181 (10.8)

Number of previous biologics, n (%)

 1

728 (43.4)

 ≥ 2

949 (56.6)

Number of previous TNFi, n (%)

 1

872 (52.0)

 ≥ 2

805 (48.0)

Treatment pattern at initiation, n (%)

 Abatacept monotherapy

112 (16.6)

427 (25.5)*

 MTX (± other csDMARDs)

436 (77.7)

947 (75.7)

  MTX alone

358 (63.8)

829 (66.3)

  MTX + other csDMARD

78 (13.9)

118 (9.4)

 Other csDMARDs

125 (22.3)

303 (24.3)

 Corticosteroids

455 (67.6)

1190 (71.0)

  > 5 mg/day

208/440 (47.3)

625/1138 (54.9)**

  ≤ 5 mg/day

232/440 (52.7)

513/1138 (45.1)

  Median dose, mg/day

5.0; n = 440

7.5; n = 1138**

Data are mean (SD) unless indicated otherwise

aCalculated

bBenign, malignant, and unspecified (neoplasms not classified as either benign or malignant). Information on malignancies at baseline was not routinely collected

cMTX and corticosteroids not taken into account

Data in italics indicate a significant difference between biologic-naive and biologic-failure groups (P < 0.05)

*P < 0.001; **P < 0.01

anti-CCP, anti-cyclic citrullinated peptide; BMI, body mass index; CDAI, Clinical Disease Activity Index; COPD, chronic obstructive pulmonary disease; CRP, C-reactive protein; csDMARD, conventional synthetic DMARD; DAS28, 28-joint Disease Activity Score; ESR, erythrocyte sedimentation rate; HAQ-DI, Health Assessment Questionnaire–Disability Index; MTX, methotrexate; PtGA, Patient Global Assessment of disease activity; RA, rheumatoid arthritis; RF, rheumatoid factor; SD, standard deviation; SDAI, Simplified Disease Activity Index; SJC28, swollen joint count in 28 joints; TJC28, Tender joint count in 28 joints; VAS visual analogue scale

Retention

A total of 2350 of the 2364 patients enrolled were evaluable at 2 years. The overall crude retention rate (95% CI) at 2 years for the evaluable patients was 47.9% (45.7, 50.0). Retention rates (95% CI) at 2 years were significantly higher in biologic-naive vs biologic-failure patients (54.5% [50.5, 58.3] vs 45.2% [42.7, 47.7], respectively; P < 0.001). Crude retention rates at 2 years decreased with increasing number of previous biologics: 50.2% (46.3, 53.9) vs 41.3% (38.0, 44.6); log-rank test: P < 0.001 for 1 vs ≥ 2 previous biologics, respectively. The difference in retention rates between each line of treatment was statistically significant (log-rank test, P < 0.001; Fig. 2). Over 2 years, the most common reasons for discontinuation of abatacept in biologic-naive and biologic-failure patients, respectively, were inefficacy (61.4% and 67.7%) and safety (21.3% and 21.2%).
Fig. 2

Crude abatacept retention rates over 2 years by treatment line

In an exploratory analysis to include the patients who discontinued IV abatacept but either switched to SC abatacept or restarted IV abatacept within 6 months (77/186 [41.4%] biologic-naive and 186/526 [35.4%] biologic-failure patients), the overall retention rate (95% CI) at 2 years was 61.2% (59.1%, 63.2%) and remained higher for biologic-naive than for biologic-failure patients (68.9% [65.1%, 72.4%] vs 58.1% [55.6%, 60.5%], respectively).

Predictors of retention

Overall, 1603 of 2350 (68.2%) evaluable patients were included in the analysis of predictors of abatacept retention. Patients with data missing for any variables tested in the model were excluded.

Biologic-naive patients

In total, four of the 27 variables tested in the univariable analysis were entered into an initial multivariable Cox proportional hazard regression model: diabetes mellitus, country, rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) serostatus, and patient’s sex. After backward selection, only three variables were retained in the final multivariable model according to statistical significance (diabetes mellitus, country, and RF and anti-CCP serostatus; Fig. 3a). Biologic-naive patients were less likely to have discontinued abatacept at 2 years if they were RF and anti-CCP double positive vs double negative at baseline (HR: 0.71; 95% CI: 0.53, 0.96; P = 0.019); single-positive vs double-negative status at baseline was not associated with a lower likelihood of abatacept discontinuation. Biologic-naive patients with diabetes mellitus were less likely than those without this co-morbidity to have discontinued abatacept (HR, 0.61; 95% CI 0.38, 0.99; P = 0.043). Abatacept retention at 2 years varied by country, with patients in Canada, Greece, and Italy less likely to have discontinued than those in Germany (P < 0.001). Patient’s sex was not identified as a predictor of retention at 2 years.
Fig. 3

Multivariable model of abatacept retention in: a biologic-naive patients; b patients with previous biologic failure

Patients with previous biologic failure

In total, six of the 31 baseline variables tested in the univariable analyses were entered into the initial multivariable model: main reason for stopping the last biologic, abatacept monotherapy vs combination therapy, country, Patient Global Assessment of disease activity (PtGA), RF and anti-CCP serostatus, and bronchospasm and obstruction co-morbidity. After backward selection, four variables were retained in the final multivariable model according to statistical significance (main reason for stopping the last biologic, abatacept monotherapy vs combination therapy, PtGA, and RF and anti-CCP serostatus; Fig. 3b). Biologic-failure patients were less likely to have discontinued abatacept at 2 years if they were RF and anti-CCP double positive vs double negative at baseline (HR, 0.76; 95% CI 0.62, 0.94; P = 0.035). Primary efficacy failure (± secondary efficacy failure, remission, or other reasons) was associated with a trend towards a higher likelihood of abatacept discontinuation at 2 years (HR, 1.28; 95% CI 1.00, 1.63; P = 0.014). Initiation of abatacept in combination with methotrexate (± other DMARDs) was less likely than initiation as monotherapy to be associated with discontinuation at 2 years (HR, 0.68; 95% CI 0.55, 0.83; P < 0.001). Biologic-failure patients with a PtGA score of ≥ 70 vs < 70 mm on a visual analogue scale (VAS) of 0–100 mm at baseline were more likely to have discontinued abatacept at 2 years (HR, 1.26; 95% CI 1.05, 1.52; P = 0.040). The country in which abatacept was initiated or a baseline co-morbidity of bronchospasm and obstruction were not identified as predictors of abatacept retention at 2 years.

Clinical outcomes

Good/moderate EULAR response rates based on DAS28 (ESR, otherwise CRP) increased over 2 years of abatacept treatment in both biologic-naive and biologic-failure patients. Of the 605 patients with data available for the evaluation of EULAR response at 2 years, the proportion of patients with a good/moderate response was higher in biologic-naive patients than in those with previous biologic failure (Fig. 4). A good or moderate EULAR response (95% CI) was attained at 2 years by 90.7% (86.8, 94.6) of patients who were biologic naive and 81.6% (77.7, 85.4) of patients with previous biologic failure (1 previous biologic failure, 81.7% [76.2, 87.2]; ≥ 2 previous biologic failures, 81.5% [76.1, 86.9]) (Fisher’s exact test, P = 0.005; Fig. 4). Overall, RF/anti-CCP positivity vs double negativity was associated with a higher good/moderate EULAR response rate at 2 years: 87.7%, 83.4%, and 75.6% in double RF/anti-CCP-positive, single RF- or anti-CCP-positive, and double RF/anti-CCP-negative patients, respectively; Fisher’s exact test P = 0.007.
Fig. 4

EULAR response over 2 years by treatment line

At 2 years, clinical remission rates were numerically higher in biologic-naive vs biologic-failure patients: DAS28 (ESR) (n = 591): 49.5 vs 35.1%; DAS28 (CRP) (n = 579): 57.1 vs 49.3%; CDAI (n = 201): 31.5 vs 27.4%; SDAI (n = 151): 32.7 vs 25.6%; and Boolean (n = 579): 28.9 vs 20.2%. In the exploratory analysis, which included the patients who had discontinued abatacept and had either switched to SC abatacept or restarted IV abatacept within 6 months, clinical remission rates at the last follow-up before discontinuation in the biologic-naive vs biologic-failure patients were DAS28 (ESR) (n = 71): 36.4 vs 18.4%; DAS28 (CRP) (n = 75): 26.1 vs 26.9%; CDAI (n = 85): 4.3 vs 4.8%; SDAI (n = 72): 13.6 vs 6.0%, and Boolean (n = 75); 4.3 vs 5.8%. Remission rates at the first follow-up after abatacept was restarted were DAS28 (ESR) (n = 189): 21.0 vs 15.0%; DAS28 (CRP) (n = 191): 35.1 vs 17.9%; CDAI (n = 219): 17.5 vs 6.4%; SDAI (n = 172): 21.6 vs 5.0%; and Boolean (n = 191): 19.3 vs 3.0%.

Treatment pattern

Changes from baseline concomitant DMARD medication over 2 years were assessed in 286 biologic-naive patients and in 564 patients with previous biologic failure. At 2 years, the pattern of abatacept co-treatment was unchanged in 89.5% of biologic-naive patients (42/47 patients who had initiated abatacept as monotherapy and 214/239 patients who had initiated abatacept as combination therapy). At the same time point, the pattern of co-treatment was unchanged in 88.3% of biologic-failure patients (100/120 patients who had initiated abatacept as monotherapy and 398/444 patients who had initiated abatacept as combination therapy). The proportions of patients co-prescribed corticosteroids with abatacept were smaller at 2 years vs baseline: 141/286 (49.3%) vs 455/673 (67.6%) biologic-naive patients, and 319/564 (56.6%) vs 1190/1677 (71.0%) biologic-failure patients. The median dose of corticosteroid co-prescribed at 2 years was unchanged from baseline in biologic-naive patients (5 mg) and decreased from 7.5 mg to 6.0 mg in biologic-failure patients.

The proportions of patients who switched between the IV and SC formulations of abatacept over 2 years were similar in both biologic-naive and biologic-failure groups (13.1% and 13.4%, respectively). Patient choice was the most common reason for switching from the IV to SC formulation in both groups (biologic-naive, 54.9% patients; biologic-failure 62.0% patients).

Safety

A total of 381 SAEs were reported in 193/2364 (8.2%) patients; 94 SAEs led to abatacept discontinuation. There were 27 deaths, 2 of which were due to opportunistic infections (Pneumocystis jirovecii; candida). Serious infections were reported in 76 patients: most were upper respiratory tract infections; others included 4 opportunistic infections (4 cases: Pneumocystis jirovecii [2 cases], cytomegalovirus [1 case], candida [1 case]), and herpes (8 cases). Malignancies were reported in 24 patients (acute myeloid leukemia [1 patient], basal cell carcinoma [5 patients], bladder neoplasm [1 patient], benign breast neoplasm [1 patient], Bowen’s disease [3 patients], brain neoplasm [1 patient], breast cancer [2 patients], melanoma [2 patients], neoplasm [1 patient], non-Hodgkin’s lymphoma [2 patients], ovarian adenoma [1 patient], pelvic mass [1 patient], and squamous cell carcinoma of the skin [1 patient]); two patients had pre-existing malignancies at baseline (brain tumor, Bowen’s disease). Serious cardiac disorders were reported in 17 patients, serious vascular disorders occurred in 15 patients and serious immune system disorders were reported in 20 patients.

Discussion

Final results from this prospective, international study of abatacept showed that, in real-world clinical practice, around 48% of patients remained on abatacept treatment at 2 years, irrespective of treatment line. In this first real-world study to include a cohort of biologic-naive patients treated with abatacept, higher abatacept retention rates at 2 years were associated with lower previous exposure to biologics: biologic-naive patients showed a retention rate of 55% compared with a rate of 45% in patients with previous biologic failure. This was consistent with findings from independent registry studies for abatacept [21, 22] and other biologics [23, 24, 25, 26]. Predictors of abatacept retention were identified using multivariable analysis. Abatacept treatment achieved continued clinical improvement over 2 years and was well tolerated; the safety profile was consistent with that previously reported in clinical trials and the real-world setting [27, 28, 29] with no new safety signals identified. In general, the current findings confirm earlier observations from interim analyses of the ACTION study [30, 31, 32, 18] and provide clinically applicable data on various parameters of disease activity in both biologic-naive patients and in those with previous biologic failure.

ACTION was a long-term, observational study of adult patients with moderate-to-severe RA who initiated IV abatacept in routine clinical practice from May 2008 to December 2013. In this first analysis of ACTION to include the full study cohort, the overall retention of abatacept at 2 years was 47.9%, lower than the 54.4% reported in a previous interim analysis which included the patients enrolled from May 2008 to December 2010 only [32]. A later year of prescription has been associated with a higher risk of discontinuation of other biologics, possibly due to an increased likelihood of a change in therapy with the availability of more treatment options [33]. The SC formulation of abatacept gained European and Canadian approval for use in moderate-to-severe RA in 2012 and 2013, respectively [10, 11]. In our exploratory analysis to include patients who, following discontinuation of IV abatacept, either switched to the SC formulation or restarted IV abatacept, overall retention at 2 years was higher than in the main analysis in which these patients were excluded.

Double positivity for both RF and anti-CCP was associated with a greater likelihood of abatacept retention than either single positivity or double negativity, irrespective of treatment line. Real-world evidence from a pooled analysis of European RA registries has previously shown that RF and anti-CCP positivity were each strongly associated with improved retention of abatacept [34]. A positive association has also been demonstrated between abatacept retention and anti-CCP positivity in patients in clinical trials [35, 36] and a registry study [37]. In contrast, evidence of an association between seropositivity and improved retention of other biologics is lacking. A good/moderate EULAR response to abatacept at 2 years was significantly associated with an RF/anti-CCP positive versus double-negative serostatus and could suggest an increased clinical response to abatacept in more severe disease. Positivity for RF and anti-CCP was reported to be similarly predictive of more successful long-term treatment of biologic-failure patients with rituximab in a registry study [23]. The underlying reasons for improved response and retention rates in patients with seropositivity are not yet fully understood; however, a recent study demonstrated that abatacept inhibits autoantibody-mediated production of inflammatory cytokines by monocytes via the induction of indoleamine 2,3-dioxygenase [38]. These inhibitory effects may explain the rapid anti-inflammatory effects of abatacept and its preferential efficacy in anti-CCP-positive patients [38].

The presence of co-morbidities is an important aspect of the therapeutic management of RA [39]; patient co-morbidity has been shown to be predictive of the discontinuation of TNFis in RA [40]. In this final 2-year analysis of ACTION, biologic-naive patients with diabetes mellitus were at a lower risk of abatacept discontinuation than those without this co-morbidity. This finding could reflect a clinician preference for abatacept in patients with RA and diabetes mellitus; however, this would require confirmation in further study. Data from healthcare claims databases suggest that abatacept is associated with a reduced risk of cardiovascular outcomes compared with TNFis in patients with RA and diabetes mellitus [41].

Although there were no local reimbursement restrictions, differences in abatacept retention by country were observed within the biologic-naive patient group in the multivariable analysis, and these were independent of patient characteristics. These differences in retention may reflect national differences in prescribing guidelines; for example, although abatacept monotherapy is approved in Europe and Canada [10, 11], clinical guidelines in Germany permit abatacept monotherapy only in patients who are intolerant of methotrexate. Differences in abatacept retention have been observed previously across countries in a pooled analysis of data from European registries and were indicative of a lack of uniformity in access to biologics [22]. Irrespective of regional variations, real-world studies continue to provide valuable data on abatacept for clinicians.

The current analysis also identified a higher baseline PtGA (≥ 70 mm on a VAS scale of 0–100 mm) and the initiation of abatacept as monotherapy vs in combination with a csDMARD as predictors of lower retention in biologic-failure patients. Patient sex was not found to be a significant predictor of abatacept retention in biologic-naive patients, consistent with the findings for retention in a population-based, observational study of patients with RA receiving biologic therapy for the first time [42].

Several interim analyses of ACTION have investigated potential predictors of clinical response in specific patient populations [31, 32, 43, 44]. Identification of predictors in heterogeneous patient populations in a clinical setting may assist the prediction of clinical response with increased accuracy and improve the ability to attain treatment targets for the optimal management of RA [2]. Although multivariable analyses to investigate predictors of response were not performed in the current analysis, double RF/anti-CCP positivity was associated with better EULAR response vs double negativity, consistent with previous real-world evidence of an association between seropositivity and improved clinical outcomes with abatacept [37, 45]. The rates for good/moderate EULAR response based on DAS28 (ESR, otherwise CRP) and DAS28 (ESR or CRP) remission at 2 years were higher in biologic-naive than in biologic-failure patients, suggesting a greater benefit with earlier treatment, and reflecting changes in the management of RA over the study period and the earlier selection of bDMARDs for patients with poor prognostic factors [2].

ACTION was an observational study of abatacept in routine practice. The study methodology did not interfere with the usual clinical care of patients with RA, very few patients were lost to follow-up, and the results generated were representative and relevant to each participating country. Inherent limitations of observational, real-world studies include referral and channeling bias, the absence of an active comparator, and loss of patients to follow-up. Moreover, as there was no requirement for the investigator to perform follow-up visits or clinical assessments consistent with other registry studies worldwide, the data generated could be incomplete. To evaluate the impact of missing data in this real-world study, the same multivariable model was performed both with and without imputation; the predictors of retention identified were consistent with the assumptions tested (data not shown).

In conclusion, abatacept retention and EULAR response rates were higher in patients who received abatacept as an earlier line of treatment and in those who were seropositive for both RF and anti-CCP; additional predictors of abatacept retention were observed by treatment line. These findings have the potential to inform the development of an individualized treatment plan for the optimal management of patients with moderate-to-severe RA.

Notes

Acknowledgments

Professional medical writing and editorial assistance was provided by Linda Brown and Mary Tetlow at Caudex and funded by Bristol-Myers Squibb.

Funding

This work was supported by Bristol-Myers Squibb.

Compliance with ethical standards

Conflict of interest

RA: grant/research support: Bristol-Myers Squibb; speakers bureau: Bristol-Myers Squibb. XM: grant/research support: Biogen, Pfizer, UCB; speakers bureau: Bristol-Myers Squibb, LFB, GSK, Pfizer, UCB. H-ML: consulting fees: AbbVie, Bristol-Myers Squibb, Roche-Chugai, UCB, MSD, GSK, Sobi, Medac, Novartis, Janssen-Cilag, AstraZeneca, Pfizer, Actelion. HN: consulting fees: AbbVie, Bristol-Myers Squibb, Celgene, Janssen, Lilly, MSD, Novartis, Pfizer, Roche, UCB. MG: none declared. FN: grant/research support: Pfizer, MSD, AbbVie, Bristol-Myers Squibb, Roche; speakers bureau: Pfizer, MSD, Roche, UCB, AbbVie, Bristol-Myers Squibb; consultant: Pfizer, MSD, Roche, UCB, AbbVie, Bristol-Myers Squibb, Janssen, Lilly. MC: employee: Bristol-Myers Squibb. JH: consultant: Bristol-Myers Squibb. CP: consultant: Bristol-Myers Squibb. CR: shareholder and employee: Bristol-Myers Squibb. MLB: shareholder and employee: Bristol-Myers Squibb (at time of study).

Ethical approval

The study was conducted in accordance with the Declaration of Helsinki, the International Conference on Harmonization Good Clinical Practice Guidelines, and the Good Epidemiological Practice Guidelines. All enrolled patients provided informed consent in accordance with local laws.

Supplementary material

10067_2019_4449_MOESM1_ESM.pdf (166 kb)
ESM 1 (PDF 166 kb)

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© The Author(s) 2019
corrected publication 2019

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Rieke Alten
    • 1
    Email author
  • Xavier Mariette
    • 2
  • Hanns-Martin Lorenz
    • 3
  • Hubert Nüßlein
    • 4
  • Mauro Galeazzi
    • 5
  • Federico Navarro
    • 6
  • Melanie Chartier
    • 7
  • Julia Heitzmann
    • 8
  • Coralie Poncet
    • 9
  • Christiane Rauch
    • 10
  • Manuela Le Bars
    • 11
    • 12
  1. 1.Department of Internal Medicine, Rheumatology, Clinical Immunology, and OsteologySchlosspark-Klinik University Medicine BerlinBerlinGermany
  2. 2.Department of RheumatologyUniversité Paris-SudParisFrance
  3. 3.Department of RheumatologyUniversity HospitalHeidelbergGermany
  4. 4.Department of Internal Medicine and RheumatologyUniversity of Erlangen-NurembergNurembergGermany
  5. 5.Department of Medical Sciences, Surgery, and NeuroscienceUniversity of SienaSienaItaly
  6. 6.Department of RheumatologyHospital Universitario Virgen MacarenaSevilleSpain
  7. 7.Marketed Product Late Stage Operation DepartmentBristol-Myers SquibbRueil-MalmaisonFrance
  8. 8.ExcelyaBoulogne-BillancourtFrance
  9. 9.Docs InternationalIssy-les-MoulineauxFrance
  10. 10.Department of ImmunoscienceBristol-Myers SquibbMunichGermany
  11. 11.Speciality Development ImmunologyBristol-Myers SquibbRueil-MalmaisonFrance
  12. 12.Janssen-Cilag European Medical Affairs Immunology-GastroenterologyIssy-les-MoulineauxFrance

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