Abstract

Predicting the response of patients with ulcerative colitis (UC) to a biologic such as vedolizumab (VDZ) before administration is an unmet need for optimizing individual patient treatment. We hypothesized that the machine-learning approach with daily clinical information can be a new, promising strategy for developing a drug-efficacy prediction tool. Random forest with grid search and cross-validation was employed in Cohort 1 to determine the contribution of clinical features at baseline (week 0) to steroid-free clinical remission (SFCR) with VDZ at week 22. Among 49 clinical features including sex, age, height, body weight, BMI, disease duration/phenotype, treatment history, clinical activity, endoscopic activity, and blood test items, the top eight features (partial Mayo score, MCH, BMI, BUN, concomitant use of AZA, lymphocyte fraction, height, and CRP) were selected for logistic regression to develop a prediction model for SFCR at week 22. In the validation using the external Cohort 2, the positive and negative predictive values of the prediction model were 54.5% and 92.3%, respectively. The prediction tool appeared useful for identifying patients with UC who would not achieve SFCR at week 22 during VDZ therapy. This study provides a proof-of-concept that machine learning using real-world data could permit personalized treatment for UC.

Highlights

  • Sex (M/F) Age Height Body weight Body mass index ulcerative colitis (UC) disease durationClinical activity of UC Lichtiger index Partial Mayo score UC disease typeTreatment history for UC 5-aminosalicylic acid (5-ASA) Azathioprine Prednisolone Anti TNF-alpha agent Tofacitinib Tacrolimus GMA Concomitant treatment for UC 5-ASA Azathioprine PrednisoloneEndoscopic activity of UC Complete blood countMayo endoscopic subscore Red blood cell (× 1­ 04/μL) UCEISHemoglobin (g/dL) UCEIS-V Hematocrit (%) UCEIS-E

  • It is an advantage of Random forest (RF) that we could investigate the contribution of these various clinical features in our cohorts despite the limited the number of subjects

  • It is challenging to assess a large number of features in detail using statistical methodology, such as univariate and multivariate analyses, which require a huge number of subjects

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Summary

Introduction

Sex (M/F) Age (years old) (median, range) Height (cm)*, # (mean, range) Body weight (kg)*, # (mean, range) Body mass index*, # (mean, range) UC disease duration (years) (median, range) UC disease type (total colitis/left-sided colitis) Treatment history for UC 5-ASA (+ /−) Azathioprine (+ /−) Prednisolone (+ /−) Anti TNF-alpha agent (+ /−) Tofacitinib (+ /−) Tacrolimus (+ /−) Granulocyte and monocyte apheresis (+ /−) Concomitant treatment for UC 5-ASA (+ /−) Azathioprine (+ /−) Prednisolone (+ /−) Clinical activity of UC Lichtiger index (median, range) Partial Mayo score (median, range) Endoscopic activity of UC (n = 31) Mayo endoscopic subscore (median, range) UCEIS UCEIS-V UCEIS-E UCEIS-B.

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