TY - JOUR
T1 - Using real-world data to dynamically predict flares during tapering of biological DMARDs in rheumatoid arthritis
T2 - development, validation, and potential impact of prediction-aided decisions
AU - van der Leeuw, Matthijs S.
AU - Messelink, Marianne A.
AU - Tekstra, Janneke
AU - Medina, Ojay
AU - van Laar, Jaap M.
AU - Haitjema, Saskia
AU - Lafeber, Floris
AU - Veris-van Dieren, Josien J.
AU - van der Goes, Marlies C.
AU - den Broeder, Alfons A.
AU - Welsing, Paco M.J.
N1 - Funding Information:
This project was made possible by the Applied Data Analytics in Medicine (ADAM) program of the University Medical Center Utrecht, Utrecht, the Netherlands. The authors would like to specifically acknowledge Prof. Dr. Wouter W. van Solinge, PhD, IR, Hyleco H. Nauta, and Harry Pijl, MBA, for their organizational support.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - BACKGROUND: Biological disease-modifying antirheumatic drugs (bDMARDs) are effective in the treatment of rheumatoid arthritis. However, as bDMARDs may also lead to adverse events and are expensive, tapering them is of great clinical interest. Tapering according to disease activity-guided dose optimization (DGDO) does not seem to affect long term remission rates, but flares are frequent during this process. Our objective was to develop a model for the prediction of flares during bDMARD tapering using data from routine care and to evaluate its potential clinical impact. METHODS: We used a joint latent class model to repeatedly predict the probability of a flare occurring within the next 3 months. The model was developed using longitudinal data on disease activity (DAS28) and other routine care data from two clinics. Predictive accuracy was assessed in cross-validation and external validation was performed with data from the DRESS (Dose REduction Strategy of Subcutaneous tumor necrosis factor inhibitors) trial. Additionally, we simulated the reduction in number of flares and bDMARD dose when implementing the model as a decision aid during bDMARD tapering in the DRESS trial. RESULTS: Data from 279 bDMARD courses were used for model development. The final model included two latent DAS28-trajectories, bDMARD type and dose, disease duration, and seropositivity. The area under the curve of the final model was 0.76 (0.69-0.83) in cross-validation and 0.68 (0.62-0.73) in external validation. In simulation of prediction-aided decisions, the mean number of flares over 18 months decreased from 1.21 (0.99-1.43) to 0.75 (0.54-0.96). The reduction in he bDMARD dose was mostly maintained, increasing from 54 to 64% of full dose. CONCLUSIONS: We developed a dynamic flare prediction model, exclusively based on data typically available in routine care. Our results show that using this model to aid decisions during bDMARD tapering may significantly reduce the number of flares while maintaining most of the bDMARD dose reduction. TRIAL REGISTRATION: The clinical impact of the prediction model is currently under investigation in the PATIO randomized controlled trial (Dutch Trial Register number NL9798).
AB - BACKGROUND: Biological disease-modifying antirheumatic drugs (bDMARDs) are effective in the treatment of rheumatoid arthritis. However, as bDMARDs may also lead to adverse events and are expensive, tapering them is of great clinical interest. Tapering according to disease activity-guided dose optimization (DGDO) does not seem to affect long term remission rates, but flares are frequent during this process. Our objective was to develop a model for the prediction of flares during bDMARD tapering using data from routine care and to evaluate its potential clinical impact. METHODS: We used a joint latent class model to repeatedly predict the probability of a flare occurring within the next 3 months. The model was developed using longitudinal data on disease activity (DAS28) and other routine care data from two clinics. Predictive accuracy was assessed in cross-validation and external validation was performed with data from the DRESS (Dose REduction Strategy of Subcutaneous tumor necrosis factor inhibitors) trial. Additionally, we simulated the reduction in number of flares and bDMARD dose when implementing the model as a decision aid during bDMARD tapering in the DRESS trial. RESULTS: Data from 279 bDMARD courses were used for model development. The final model included two latent DAS28-trajectories, bDMARD type and dose, disease duration, and seropositivity. The area under the curve of the final model was 0.76 (0.69-0.83) in cross-validation and 0.68 (0.62-0.73) in external validation. In simulation of prediction-aided decisions, the mean number of flares over 18 months decreased from 1.21 (0.99-1.43) to 0.75 (0.54-0.96). The reduction in he bDMARD dose was mostly maintained, increasing from 54 to 64% of full dose. CONCLUSIONS: We developed a dynamic flare prediction model, exclusively based on data typically available in routine care. Our results show that using this model to aid decisions during bDMARD tapering may significantly reduce the number of flares while maintaining most of the bDMARD dose reduction. TRIAL REGISTRATION: The clinical impact of the prediction model is currently under investigation in the PATIO randomized controlled trial (Dutch Trial Register number NL9798).
KW - Applied data analytics in medicine
KW - Biologicals
KW - Predictive algorithm
KW - Rheumatoid arthritis
KW - Tapering bDMARD therapy
KW - Humans
KW - Arthritis, Rheumatoid/drug therapy
KW - Hydrolases
KW - Male
KW - Treatment Outcome
KW - Antirheumatic Agents/therapeutic use
KW - Biological Products/therapeutic use
UR - http://www.scopus.com/inward/record.url?scp=85126900397&partnerID=8YFLogxK
U2 - 10.1186/s13075-022-02751-8
DO - 10.1186/s13075-022-02751-8
M3 - Article
C2 - 35321739
AN - SCOPUS:85126900397
SN - 1478-6362
VL - 24
SP - 1
EP - 11
JO - Arthritis research & therapy
JF - Arthritis research & therapy
IS - 1
M1 - 74
ER -