MRI-based interpretable deep learning radiomics for predicting treatment response in axial spondyloarthritis.

BACKGROUND

The clinical efficacy of tumor necrosis factor inhibitors (TNFi) in axial spondyloarthritis (axSpA) is limited by high non-response rates, necessitating accurate pre-treatment stratification. This study aimed to develop and validate MRI-based interpretable deep learning radiomics (DLR) models to predict treatment response to TNFi in patients with axSpA.

METHODS

In this prospective study, patients diagnosed with axSpA who underwent sacroiliac joint MRI before TNFi initiation were enrolled. Patients were allocated to training and test sets at an approximate 4:1 ratio. The endpoints were major (ASAS40) and moderate (ASAS20) improvement, as defined by the Assessment of SpondyloArthritis International Society criteria. Deep learning and radiomics features were extracted from MRI. A four-step selection process, including reproducibility analysis, univariable filtering, redundancy reduction, and LASSO regression, was used to distill robust predictors. These were then integrated with clinical data to build DLR-clinical (DLRC) models using L2-regularized logistic regression.

RESULTS

A total of 183 patients (mean age, 26.5 ± 9.0 years; 121 [66.1%] males) were analyzed. The DLRC models were validated on the independent test set, with high area under the receiver operating characteristic curve (AUC) values for predicting ASAS40 (0.876, 95%CI: 0.738-0.973) and ASAS20 (0.886, 95%CI: 0.753-0.978) responses. Calibration curves indicated good model agreement, and decision curve analysis (DCA) confirmed their clinical utility. Compared to the clinical-only model, the DLRC models showed significant integrated discrimination improvement (IDI) for ASAS40 and ASAS20 (0.234 and 0.283, all p < 0.05) prediction, respectively.

CONCLUSION

MRI-based interpretable DLR models accurately predicted TNFi treatment response in axSpA patients, offering a non-invasive tool to guide personalized therapy.