Predictors of treatment response in a lupus nephritis population: lessons from the Aspreva Lupus Management Study (ALMS) trial
Authors
Yiu, Sean
Su, Li
Gordon, Caroline
Truman, Matt
Lisk, Laura
Solomons, Neil
for the MASTERPLANS Consortium
Payne, Katherine
Lunt, Mark
Peek, Niels
Geifman, Nophar
Gavan, Sean
Armitt, Gillian
Doherty, Patrick
Prattley, Jennifer
Azadbakht, Narges
Papazian, Angela
Sueur, Helen Le
Farrelly, Carmen
Richardson, Clare
Shabbir, Zunnaira
Hewitt, Lauren
McHugh, Neil
Reynolds, John
Young, Stephen
Jayne, David
Farewell, Vern
Pickering, Matthew
Lightstone, Elizabeth
Gilmore, Alyssa
Botto, Marina
Vyse, Timothy
Morris, David Lester
D’Cruz, D
Vital, Edward
Wittmann, Miriam
Emery, Paul
Beresford, Michael
Hedrich, Christian
Midgley, Angela
Gritzfeld, Jenna
Ehrenstein, Michael
Isenberg, David
Parvaz, Mariea
Dunnage, Jane
Batchelor, Jane
Holland, E
Upsall, Pauline
Publication Date
2022-05-30Journal Title
Lupus Science & Medicine
Publisher
BMJ Publishing Group
Volume
9
Issue
1
Language
en
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
McDonald, S., Yiu, S., Su, L., Gordon, C., Truman, M., Lisk, L., Solomons, N., et al. (2022). Predictors of treatment response in a lupus nephritis population: lessons from the Aspreva Lupus Management Study (ALMS) trial. Lupus Science & Medicine, 9 (1) https://doi.org/10.1136/lupus-2021-000584
Abstract
Objectives: To identify predictors of overall lupus and lupus nephritis (LN) responses in patients with LN. Methods: Data from the Aspreva Lupus Management Study (ALMS) trial cohort was used to identify baseline predictors of response at 6 months. Endpoints were major clinical response (MCR), improvement, complete renal response (CRR) and partial renal response (PRR). Univariate and multivariate logistic regressions with least absolute shrinkage and selection operator (LASSO) and cross-validation in randomly split samples were utilised. Predictors were ranked by the percentage of times selected by LASSO and prediction performance was assessed by the area under the receiver operating characteristics (AUROC) curve. Results: We studied 370 patients in the ALMS induction trial. Improvement at 6 months was associated with older age (OR=1.03 (95% CI: 1.01 to 1.05) per year), normal haemoglobin (1.85 (1.16 to 2.95) vs low haemoglobin), active lupus (British Isles Lupus Assessment Group A or B) in haematological and mucocutaneous domains (0.61 (0.39 to 0.97) and 0.50 (0.31 to 0.81)), baseline damage (SDI>1 vs =0) (0.38 (0.16 to 0.91)) and 24-hour urine protein (0.63 (0.50 to 0.80)). LN duration 2–4 years (0.43 (0.19 to 0.97) vs <1 year) and 24-hour urine protein (0.63 (0.45 to 0.89)) were negative predictors of CRR. LN duration 2–4 years (0.45 (0.24 to 0.83) vs <1 year) negatively predicted PRR. The AUROCs of models for improvement, CRR and PRR were 0.56, 0.55 and 0.51 respectively. Conclusions: Baseline variables predicted 6-month outcomes in patients with SLE. While the modest performance of models emphasises the need for new biomarkers to advance this field, the factors identified can help identify those patients who may require novel treatment strategies.
Keywords
Biomarker studies, 1506, 2253, cyclophosphamide, treatment, lupus nephritis
Identifiers
lupus-2021-000584
External DOI: https://doi.org/10.1136/lupus-2021-000584
This record's URL: https://www.repository.cam.ac.uk/handle/1810/337770
Rights
Licence:
https://creativecommons.org/licenses/by/4.0/
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