Predictors of rituximab efficacy in systemic sclerosis-associated interstitial lung disease: machine-learning analysis of the DESIRES trial

Rheumatology (Oxford). 2025 Dec 1;64(SI):SI114-SI121. doi: 10.1093/rheumatology/keae716.

Abstract

Objectives: Rituximab is emerging as a promising therapeutic option for systemic sclerosis-associated interstitial lung disease (SSc-ILD). However, little is known about factors that predict the efficacy of rituximab in SSc-ILD.

Methods: A post-hoc analysis was performed on prospective data from 48 patients with SSc-ILD in the double-blind, randomized, placebo-controlled DESIRES trial. A total of 28 baseline factors were selected as candidates to predict the efficacy of rituximab on the percentage of predicted forced vital capacity (ppFVC) at 24 weeks. A machine learning causal tree algorithm was used to explore the combination of predictors to identify subpopulations with a good response to rituximab.

Results: Serum levels of C-reactive protein (CRP) and Krebs von den Lungen-6 (KL-6) were selected as branches of the decision tree to stratify patients into three subpopulations. In the subpopulation with serum CRP levels ≥0.055 mg/dl, ΔppFVC was significantly higher in the rituximab group than in the placebo group [difference 8.01% (95% CI: 4.40%, 11.62%)]. In the subpopulation with serum CRP levels <0.055 mg/dl and serum KL-6 levels ≥364 U/ml, ΔppFVC was comparable between the two groups [difference 2.47% (95% CI: -1.99%, 6.92%)]. In the subpopulation with serum CRP levels <0.055 mg/dl and serum KL-6 levels <364 U/ml, ΔppFVC was significantly lower in rituximab than in placebo [difference -6.85% (95% CI: -10.80%, -2.91%)].

Conclusion: Even slight elevations in serum CRP levels are associated with the improvement in ppFVC and may serve as predictors of rituximab efficacy in SSc-ILD.

Keywords: interstitial lung disease; machine learning; rituximab; systemic sclerosis.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Antirheumatic Agents* / therapeutic use
  • C-Reactive Protein / analysis
  • C-Reactive Protein / metabolism
  • Double-Blind Method
  • Female
  • Humans
  • Lung Diseases, Interstitial* / blood
  • Lung Diseases, Interstitial* / drug therapy
  • Lung Diseases, Interstitial* / etiology
  • Lung Diseases, Interstitial* / physiopathology
  • Machine Learning*
  • Male
  • Middle Aged
  • Mucin-1 / blood
  • Prospective Studies
  • Rituximab* / therapeutic use
  • Scleroderma, Systemic* / complications
  • Scleroderma, Systemic* / drug therapy
  • Treatment Outcome
  • Vital Capacity

Substances

  • Rituximab
  • C-Reactive Protein
  • Mucin-1
  • Antirheumatic Agents
  • MUC1 protein, human