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Abstract Number: 2865

Methotrexate and Leflunomide Survival in Patients with Psoriatic Arthritis

Margarita Landi1, Cecilia Zaffarana1, Osvaldo Luis Cerda1, Josefina Gallino Yanzi1, Emilce Schneeberger1, Ignacio Carrillo1, María del Carmen Gonzalez Guzmán1, Jose A Maldonado Cocco1 and Gustavo Citera2, 1Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina, 2Rheumatology, Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: methotrexate (MTX) and psoriatic arthritis

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Session Information

Date: Tuesday, November 10, 2015

Title: Spondylarthropathies and Psoriatic Arthritis - Clinical Aspects and Treatment Poster III: Therapy

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose:

Disease Modifying Anti-Rheumatic Drugs (DMARDs) are frequently used in Psoriatic Arthritis (PsA), however there is limited data regarding their survival rates. This study attempts to estimate the survival rate of the most frequently used DMARDs in a cohort of PsA patients and to determine the main causes of drug discontinuation as well as factors associated with a higher survival rate.

Methods:

Patients with PsA according to CASPAR criteria, ≥ 18 years of age, belonging to the RAPSODIA cohort were studied. Socio-demographic and clinical data were collected. Peripheral, cutaneous and axial involvement were assessed along with functional status, quality of life and disease activity. Data regarding treatment was gathered by a direct interview with the patient and from medical records in order to reduce forgetfulness bias. Statistical analysis: Continuous variables were compared using Mann Whitney or T test with Levene’s test for homogeneity of variance, and categorical data by Chi2 or Fisher’s exact test. Kaplan Meier survival curves and log rank were used to analyse and compare drugs’ survival rate. Cox proportional analysis was performed to determine associated factors with drug survival.

Results:

A total of 87 patients with PsA were included in the analysis, with a median age of 52 years (IQR 40.2-61.7) and a slight female predominance (52.9%). Median disease duration was 10 years (IQR 6-17). Seventy patients (80.5%) received methotrexate (MTX), 23 (32.9%) had to discontinue it due to adverse events (65%) or treatment failure (35%). The median survival time of MTX was 13 years (range 8.5-17.4). The cumulative survival rate after 10 years of treatment was 55%, being significantly higher among patients receiving concomitant steroid therapy (Ẋ16.4±2.3 years vs Ẋ10±2 years, p=0.01).

Of the 16 patients receiving leflunomide (LFN), 56.25% had to discontinue, estimating a median survival time of 6 years (Range 1.6-10.3). The main reasons for discontinuation were adverse events (44.5%) and treatment failure (33.3%). The cumulative survival rate after 10 years was 35%. Patient’s age had a mayor impact in LFN survival; using a cut-off value of 50 years, elderly patients had higher drug survival (Ẋ5.5±1.5 years vs Ẋ3.3±1 years, p=0.03).

Conclusion:

In this cohort of PsA patients, MTX was the most frequently DMARD used, followed by LFN. MTX cumulative survival was greater than that of LFN and was favoured by concomitant steroid therapy. LFN survival was higher amongst patients with more than 50 years of age. The main reasons for drug discontinuation in both scenarios were adverse events and loss of efficacy. 


Disclosure: M. Landi, None; C. Zaffarana, None; O. L. Cerda, None; J. Gallino Yanzi, None; E. Schneeberger, None; I. Carrillo, None; M. D. C. Gonzalez Guzmán, None; J. A. Maldonado Cocco, None; G. Citera, None.

To cite this abstract in AMA style:

Landi M, Zaffarana C, Cerda OL, Gallino Yanzi J, Schneeberger E, Carrillo I, Gonzalez Guzmán MDC, Maldonado Cocco JA, Citera G. Methotrexate and Leflunomide Survival in Patients with Psoriatic Arthritis [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/methotrexate-and-leflunomide-survival-in-patients-with-psoriatic-arthritis/. Accessed .
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