A Machine Learning Approach for High-Dimensional Time-to-Event Prediction With Application to Immunogenicity of Biotherapies in the ABIRISK Cohort

被引:3
作者
Duhaze, Julianne [1 ,2 ]
Hassler, Signe [2 ,3 ,4 ]
Bachelet, Delphine [2 ,5 ]
Gleizes, Aude [6 ,7 ]
Hacein-Bey-Abina, Salima [6 ,8 ]
Allez, Matthieu [9 ]
Deisenhammer, Florian [10 ]
Fogdell-Hahn, Anna [11 ]
Mariette, Xavier [12 ]
Pallardy, Marc [7 ]
Broet, Philippe [1 ,2 ]
机构
[1] Ste Justine Hosp, Res Ctr, Montreal, PQ, Canada
[2] Paris Saclay Univ, Paul Brousse Hosp, Fac Med, INSERM,CESP,UMR 1018, Villejuif, France
[3] Sorbonne Univ, Immunol Immunopathol Immunotherapy i3, INSERM, UMR 959, Paris, France
[4] Hop La Pitie Salpetriere, AP HP, Biotherapy CIC BTi, Paris, France
[5] Hop Xavier Bichat, AP HP Nord, Dept Biostat Epidemiol & Clin Res, INSERM,CIC EC 1425, Paris, France
[6] Paris Saclay Univ, Le Kremlin Bicetre Hosp, AP HP, Clin Immunol Lab, Le Kremlin Bicetre, France
[7] Paris Saclay Univ, Fac Pharm, INSERM, UMR 996, Chatenay Malabry, France
[8] Paris Descartes Sorbonne Cite Univ, Fac Pharm, CNRS, UTCBS,UMR 8258, Paris, France
[9] Paris Diderot Univ, St Louis Hosp, AP HP, Dept Gastroenterol, Paris, France
[10] Innsbruck Med, Innsbruck, Austria
[11] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[12] Univ Paris Saclay, AP HP, Ctr Immunol Viral Infect & Autoimmune Dis, INSERM,UMR 1184, Paris, France
关键词
immunogenicity; biotherapy; machine learning; survival random forest; prediction;
D O I
10.3389/fimmu.2020.00608
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Predicting immunogenicity for biotherapies using patient and drug-related factors represents nowadays a challenging issue. With the growing ability to collect massive amount of data, machine learning algorithms can provide efficient predictive tools. From the bio-clinical data collected in the multi-cohort of autoimmune diseases treated with biotherapies from the ABIRISK consortium, we evaluated the predictive power of a custom-built random survival forest for predicting the occurrence of anti-drug antibodies. This procedure takes into account the existence of a population composed of immune-reactive and immune-tolerant subjects as well as the existence of a tiny expected proportion of relevant predictive variables. The practical application to the ABIRISK cohort shows that this approach provides a good predictive accuracy that outperforms the classical survival random forest procedure. Moreover, the individual predicted probabilities allow to separate high and low risk group of patients. To our best knowledge, this is the first study to evaluate the use of machine learning procedures to predict biotherapy immunogenicity based on bioclinical information. It seems that such approach may have potential to provide useful information for the clinical practice of stratifying patients before receiving a biotherapy.
引用
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页数:10
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