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PrCRS: a prediction model of severe CRS in CAR-T therapy based on transfer learning.
Wei, Zhenyu; Zhao, Chengkui; Zhang, Min; Xu, Jiayu; Xu, Nan; Wu, Shiwei; Xin, Xiaohui; Yu, Lei; Feng, Weixing.
Afiliación
  • Wei Z; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China. 952376687@hrbeu.edu.cn.
  • Zhao C; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China.
  • Zhang M; Shanghai Unicar-Therapy BioMedicine Technology Co., Ltd, Shanghai, China.
  • Xu J; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China.
  • Xu N; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China.
  • Wu S; School of Chemical and Molecular Engineering, East China Normal University, Zhongshan North Street, Shanghai, 200000, People's Republic of China.
  • Xin X; Shanghai Unicar-Therapy BioMedicine Technology Co., Ltd, Shanghai, China.
  • Yu L; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China.
  • Feng W; Intelligent Systems Science and Engineering College, Harbin Engineering University, Liaoyuan Street, Harbin, 150006, Heilongjiang Province, People's Republic of China.
BMC Bioinformatics ; 25(1): 197, 2024 May 20.
Article en En | MEDLINE | ID: mdl-38769505
ABSTRACT

BACKGROUND:

CAR-T cell therapy represents a novel approach for the treatment of hematologic malignancies and solid tumors. However, its implementation is accompanied by the emergence of potentially life-threatening adverse events known as cytokine release syndrome (CRS). Given the escalating number of patients undergoing CAR-T therapy, there is an urgent need to develop predictive models for severe CRS occurrence to prevent it in advance. Currently, all existing models are based on decision trees whose accuracy is far from meeting our expectations, and there is a lack of deep learning models to predict the occurrence of severe CRS more accurately.

RESULTS:

We propose PrCRS, a deep learning prediction model based on U-net and Transformer. Given the limited data available for CAR-T patients, we employ transfer learning using data from COVID-19 patients. The comprehensive evaluation demonstrates the superiority of the PrCRS model over other state-of-the-art methods for predicting CRS occurrence. We propose six models to forecast the probability of severe CRS for patients with one, two, and three days in advance. Additionally, we present a strategy to convert the model's output into actual probabilities of severe CRS and provide corresponding predictions.

CONCLUSIONS:

Based on our findings, PrCRS effectively predicts both the likelihood and timing of severe CRS in patients, thereby facilitating expedited and precise patient assessment, thus making a significant contribution to medical research. There is little research on applying deep learning algorithms to predict CRS, and our study fills this gap. This makes our research more novel and significant. Our code is publicly available at https//github.com/wzy38828201/PrCRS . The website of our prediction platform is http//prediction.unicar-therapy.com/index-en.html .
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoterapia Adoptiva / Aprendizaje Profundo / Síndrome de Liberación de Citoquinas / COVID-19 Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoterapia Adoptiva / Aprendizaje Profundo / Síndrome de Liberación de Citoquinas / COVID-19 Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article