Predicting the efficiency of chidamide in patients with angioimmunoblastic T-cell lymphoma using machine learning algorithm

被引:0
作者
Zhang, Chunlan [1 ]
Xu, Juan [1 ]
Gu, Mingyu [2 ,3 ]
Tang, Yun [1 ]
Tang, Wenjiao [1 ]
Wang, Jie [1 ]
Liu, Qinyu [1 ]
Yang, Yunfan [1 ]
Zhong, Xushu [1 ]
Xu, Caigang [1 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Hematol, Dept Hematol, Chengdu, Peoples R China
[2] Sichuan Univ, West China Sch Med, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Chengdu, Peoples R China
关键词
machine learning; chidamide; prognosis; angioimmunoblastic T-cell lymphoma; biomarker;
D O I
10.3389/fphar.2024.1435284
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Chidamide is subtype-selective histone deacetylase (HDAC) inhibitor that showed promising result in clinical trials to improve prognosis of angioimmunoblastic T-cell lymphoma (AITL) patients. However, in real world settings, contradictory reports existed as to whether chidamide improve overall survival (OS). Therefore, we aimed to develop an interpretable machine learning (Machine learning)-based model to predict the 2-year overall survival of AITL patients based on chidamide usage and baseline features.Methods A total of 183 patients with AITL were randomly divided into training set and testing set. We used 5 ML algorithms to build predictive models. Recursive feature elimination (RFE) method was used to filter for the most important features. The ML models were interpreted and the relevance of the selected features was determined using the Shapley additive explanations (SHAP) method and the local interpretable model-agnostic explanationalgorithm.Results A total of 183 patients with newly diagnosed AITL from 2012 to 2022 from 3 centers in China were enrolled in our study. Seventy-one patients were dead within 2 years after diagnosis. Five ML algorithms were built based on chidamide usage and 16 baseline features to predict 2-year OS. Catboost model presented to be the best predictive model. After RFE screening, 12 variables demonstrated the best performance (AUC = 0.8651). Using chidamide ranked third among all the variables that correlated with 2-year OS.Conclusion This study demonstrated that the Catboost model with 12 variables could effectively predict the 2-year OS of AITL patients. Combining chidamide in the treatment therapy was positively correlated with longer OS of AITL patients.
引用
收藏
页数:9
相关论文
共 22 条
  • [1] Outcomes and prognostic factors in angioimmunoblastic T-cell lymphoma: final report from the international T-cell Project
    Advani, Ranjana H.
    Skrypets, Tetiana
    Civallero, Monica
    Spinner, Michael A.
    Manni, Martina
    Kim, Won Seog
    Shustov, Andrei R.
    Horwitz, Steven M.
    Hitz, Felicitas
    Cabrera, Maria Elena
    Dlouhy, Ivan
    Vassallo, Jose
    Pileri, Stefano A.
    Inghirami, Giorgio
    Montoto, Silvia
    Vitolo, Umberto
    Radford, John
    Vose, Julie M.
    Federico, Massimo
    [J]. BLOOD, 2021, 138 (03) : 213 - 220
  • [2] RHOA G17V Induces T Follicular Helper Cell Specification and Promotes Lymphomagenesis
    Cortes, Jose R.
    Ambesi-Impiombato, Alberto
    Couronne, Lucile
    Quinn, S. Aidan
    Kim, Christine S.
    Almeida, Ana C. da Silva
    West, Zachary
    Belver, Laura
    Martin, Marta Sanchez
    Scourzic, Laurianne
    Bhagat, Govind
    Bernard, Olivier A.
    Ferrando, Adolfo A.
    Palomero, Teresa
    [J]. CANCER CELL, 2018, 33 (02) : 259 - +
  • [3] Artificial intelligence in cancer research, diagnosis and therapy
    Elemento, Olivier
    Leslie, Christina
    Lundin, Johan
    Tourassi, Georgia
    [J]. NATURE REVIEWS CANCER, 2021, 21 (12) : 747 - 752
  • [4] CS055 (Chidamide/HBI-8000), a novel histone deacetylase inhibitor, induces G1 arrest, ROS-dependent apoptosis and differentiation in human leukaemia cells
    Gong, Ke
    Xie, Jia
    Yi, Hong
    Li, Wenhua
    [J]. BIOCHEMICAL JOURNAL, 2012, 443 : 735 - 746
  • [5] Chidamide Maintenance Therapy Following Induction Therapy in Patients With Peripheral T-Cell Lymphoma Who Are Ineligible for Autologous Stem Cell Transplantation: Case Series From China
    Guo, Wei
    Wang, Xingtong
    Li, Jia
    Yin, Xianying
    Zhao, Yangzhi
    Tang, Yang
    Wang, Anna
    Bai, Ou
    [J]. FRONTIERS IN ONCOLOGY, 2022, 12
  • [6] Comparison of four prognostic scores in peripheral T-cell lymphoma
    Gutierrez-Garcia, G.
    Garcia-Herrera, A.
    Cardesa, T.
    Martinez, A.
    Villamor, N.
    Ghita, G.
    Martinez-Trillos, A.
    Colomo, L.
    Setoain, X.
    Rodriguez, S.
    Gine, E.
    Campo, E.
    Lopez-Guillermo, A.
    [J]. ANNALS OF ONCOLOGY, 2011, 22 (02) : 397 - 404
  • [7] Artificial Intelligence and Machine Learning in Clinical Medicine, 2023
    Haug, Charlotte J. J.
    Drazen, Jeffrey M. M.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2023, 388 (13) : 1201 - 1208
  • [8] T-Cell Lymphomas, Version 2.2022
    Horwitz, Steven M.
    Ansell, Stephen
    Ai, Weiyun Z.
    Barnes, Jeffrey
    Barta, Stefan K.
    Brammer, Jonathan
    Clemens, Mark W.
    Dogan, Ahmet
    Foss, Francine
    Ghione, Paola
    Goodman, Aaron M.
    Guitart, Joan
    Halwani, Ahmad
    Haverkos, Bradley M.
    Hoppe, Richard T.
    Jacobsen, Eric
    Jagadeesh, Deepa
    Jones, Allison
    Kallam, Avyakta
    Kim, Youn H.
    Kumar, Kiran
    Mehta-Shah, Neha
    Olsen, Elise A.
    Rajguru, Saurabh A.
    Rozati, Sima
    Said, Jonathan
    Shaver, Aaron
    Shea, Lauren
    Shinohara, Michi M.
    Sokol, Lubomir
    Torres-Cabala, Carlos
    Wilcox, Ryan
    Wu, Peggy
    Zain, Jasmine
    Dwyer, Mary
    Sundar, Hema
    [J]. JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2022, 20 (03): : 285 - 308
  • [9] Development of a Novel Clinical Prognostic Model for Patients With Angioimmunoblastic T-Cell Lymphoma
    Huang, Chen
    Zhang, Huichao
    Gao, Yuhuan
    Diao, Lanping
    Liu, Lihong
    [J]. TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2020, 19
  • [10] IDH2 and TET2 mutations synergize to modulate T Follicular Helper cell functional interaction with the AITL microenvironment
    Leca, Julie
    Lemonnier, Francois
    Meydan, Cem
    Foox, Jonathan
    El Ghamrasni, Samah
    Mboumba, Diana-Laure
    Duncan, Gordon S.
    Fortin, Jerome
    Sakamoto, Takashi
    Tobin, Chantal
    Hodgson, Kelsey
    Haight, Jillian
    Smith, Logan K.
    Elia, Andrew J.
    Butler, Daniel
    Berger, Thorsten
    de Leval, Laurence
    Mason, Christopher E.
    Melnick, Ari
    Gaulard, Philippe
    Mak, Tak W.
    [J]. CANCER CELL, 2023, 41 (02) : 323 - +