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Abstract Number: 1795

Therapeutic Strategies for Patients with Chronic Manifestations of Calcium Pyrophosphate Deposition Disease

Julien Damart1, Silvia Sirotti2, Mariano Andrès3, Edoardo Cipolletta4, Georgios Filippou5, Davide Carboni6, Emilio Filippucci7, Pilar Diez8, Abhishek Abhishek9, Augustin Latourte10, Hang-Korng Ea11, Sebastien Ottaviani12, Jean-Guillaume Letarouilly13, Renaud Desbarbieux14, Sahara Graf1, Laurène Norberciak1, Pascal Richette15 and Tristan Pascart16, 1Hôpital Saint-Philibert, Lomme, France, 2Università degli Studi di Milano, Milano, Italy, 3Dr Balmis Alicante General University Hospital-ISABIAL, Alicante, Spain, 4Polytechnic University of Marche, Ancona, Italy, 5Rheumatology Department, Luigi Sacco University Hospital, Siena, Italy, 6Luigi Sacco University, Milano, Italy, 7Polytechnic University of Marche, Rheumatology Unit, Department of Clinical and Molecular Sciences, "Carlo Urbani" Hospital, Jesi, Italy, 8Alicante University, Alicante, Spain, 9University of Nottingham, Nottingham, United Kingdom, 10Université de Paris, Paris, France, 11Lariboisière Hospital, Paris, France, 12Hopital Bichat-Claude Bernard, Paris, France, 13CHU Lille, Lille, France, 14Ch Boulogne-sur-Mer, Boulogne-sur-Mer, France, 15Department of Rheumatology, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris, Paris, France, 16Groupement Hospitalier de l'Institut Catholique de Lille, Lomme, France

Meeting: ACR Convergence 2022

Keywords: Biologicals, corticosteroids, CPPD

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Session Information

Date: Monday, November 14, 2022

Title: Metabolic and Crystal Arthropathies – Basic and Clinical Science Poster

Session Type: Poster Session D

Session Time: 1:00PM-3:00PM

Background/Purpose: Calcium pyrophosphate deposition (CPPD) disease lacks recommendations on treatment strategies. This study reports on treatment modalities used in European tertiary hospitals for the management of patients with chronic CPPD disease.

Methods: Charts from patients with a diagnosis of chronic CPPD disease were retrospectively reviewed. Chronic CPPD disease was defined as persistent CPP crystal inflammatory arthritis lasting for more than 3 months and/or recurrent ( >2 episodes/year) acute episodes of CPP crystal arthritis. Patients came from 4 centers in France, 1 in Spain and 2 in Italy. All treatments started from the 1st of January 2015 were recorded.

Baseline characteristics of patients were collected, including clinical presentation, items for CPPD diagnosis, disease activity (Patient Global Assessment (PGA) 0-10 on a numeric scale), quality of life on a 0 to 4 Likert scale, and treatments before 2015. The median number [inter-quartile range] of treatments used prior to each new treatment initiated was noted. Visits at baseline, months 3, 6, 12 and 24 were recorded for each new treatment initiated. Treatment efficacy was assessed with a 0 to 4 Likert scale according to the data from the files of the patients. If the treatment was discontinued before the 24 months visit, the date and cause was recorded.

Results: A total of 129 patients were included in the study (n = 66 in France, n = 21 in Spain, and n = 42 in Italy), cumulating n=194 treatments initiated since 2015, and a mean number of 1.8 (±0.9) treatments per patient. Mean age was 69.6 ± 13.1 years, n = 83 (64.3%) were females, duration of symptoms before the first recorded treatment was 16.8 (±27.1) months. Overall, n = 85 (65.9%) patients presented with persistent CPP crystal inflammatory arthritis and n = 83 (64.3%) presented with recurrent acute episodes of CPP crystal arthritis flares. Mean PGA at baseline was 6.6 ± 1.5, resulting in impaired quality of life (< 4 on the Likert scale) in 94.6% of patients.

The most frequent first-line therapy was colchicine in n= 83 (72.8%) patients (mainly 1mg QD (57.8%) and 0.5mg QD (33.7%) QID). At 24 months, n = 49 (59.0%) of patients were still on colchicine, n = 25 (30.1%) had discontinued colchicine for inefficacy, n = 4 (4.8%) for intolerance, and n = 5 (6.0%) for prolonged symptom remission.

The median position of each treatment in the therapeutic strategy, drug retention and treatment efficacy are reported in Table 1. Treatment retention for drugs with at least 20 initiations are reported in Figure 1. Combination of treatments was prescribed in 35 patients (27.1%), mostly using corticosteroids (n = 20, 66.7% of combinations).

Conclusion: This study shows that long term colchicine is the most frequent first-line therapy prescribed for chronic CPPD disease in a variety of European centers. Methotrexate is still significantly used, while anakinra and tocilizumab are the most frequent biological therapies. Although this is an uncontrolled study, our results call for adequately powered clinical trials evaluating the efficacy of hydroxychloroquine, methotrexate, colchicine and biological agents in persistent CPP crystal arthritis and recurrent acute CPP crystal arthritis.

Supporting image 1

Table 1.Treatment positionning in the therapeutic startegy, drug retention and efficacy of treatments used for the management of chronic manifestations of calcium pyrophosphate deposition disease.

Supporting image 2

Figure 1. Kaplan-Meyer survival plots of colchicine, methotrexate, anakinra and tocilizumab for the treatment of chronic manifestations of calcium pyrophsophate deposition disease.


Disclosures: J. Damart, None; S. Sirotti, None; M. Andrès, Menarini, Grunenthal; E. Cipolletta, None; G. Filippou, None; D. Carboni, None; E. Filippucci, None; P. Diez, None; A. Abhishek, AstraZeneca, Pfizer, Oxford immunotec, Inflazome, NGMBiopharmaceuticals, Uptodate, Cadilla pharmaceuticals; A. Latourte, None; H. Ea, None; S. Ottaviani, None; J. Letarouilly, None; R. Desbarbieux, None; S. Graf, None; L. Norberciak, None; P. Richette, AbbVie, Amgen, Biogen, Bristol Myers Squibb, Celgene, Eli Lilly, Janssen, Novartis, Pfizer, Roche, Sanofi-Aventis, UCB; T. Pascart, None.

To cite this abstract in AMA style:

Damart J, Sirotti S, Andrès M, Cipolletta E, Filippou G, Carboni D, Filippucci E, Diez P, Abhishek A, Latourte A, Ea H, Ottaviani S, Letarouilly J, Desbarbieux R, Graf S, Norberciak L, Richette P, Pascart T. Therapeutic Strategies for Patients with Chronic Manifestations of Calcium Pyrophosphate Deposition Disease [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/therapeutic-strategies-for-patients-with-chronic-manifestations-of-calcium-pyrophosphate-deposition-disease/. Accessed .
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