Skip to Main Content (Press Enter)

Logo UNISR
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills

UNIFIND
Logo UNISR

|

UNIFIND

unisr.it
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills
  1. Outputs

Determining clinical course of diffuse large B-cell lymphoma using targeted transcriptome and machine learning algorithms

Academic Article
Publication Date:
2022
Short description:
Determining clinical course of diffuse large B-cell lymphoma using targeted transcriptome and machine learning algorithms / Albitar, M., Zhang, H., Goy, A., Xu-Monette, Z.Y., Bhagat, G., Visco, C., Tzankov, A., Fang, X., Zhu, F., Dybkaer, K., Chiu, A., Tam, W., Zu, Y., Hsi, E.D., Hagemeister, F.B., Huh, J., Ponzoni, M., Ferreri, A.J.M., Moller, M.B., Parsons, B.M., et al.. - In: BLOOD CANCER JOURNAL. - ISSN 2044-5385. - 12:2(2022). [10.1038/s41408-022-00617-5]
abstract:
Multiple studies have demonstrated that diffuse large B-cell lymphoma (DLBCL) can be divided into subgroups based on their biology; however, these biological subgroups overlap clinically. Using machine learning, we developed an approach to stratify patients with DLBCL into four subgroups based on survival characteristics. This approach uses data from the targeted transcriptome to predict these survival subgroups. Using the expression levels of 180 genes, our model reliably predicted the four survival subgroups and was validated using independent groups of patients. Multivariate analysis showed that this patient stratification strategy encompasses various biological characteristics of DLBCL, and only TP53 mutations remained an independent prognostic biomarker. This novel approach for stratifying patients with DLBCL, based on the clinical outcome of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone therapy, can be used to identify patients who may not respond well to these types of therapy, but would otherwise benefit from alternative therapy and clinical trials.
Iris type:
1.1 Articolo in rivista
List of contributors:
Albitar, M.; Zhang, H.; Goy, A.; Xu-Monette, Z. Y.; Bhagat, G.; Visco, C.; Tzankov, A.; Fang, X.; Zhu, F.; Dybkaer, K.; Chiu, A.; Tam, W.; Zu, Y.; Hsi, E. D.; Hagemeister, F. B.; Huh, J.; Ponzoni, M.; Ferreri, A. J. M.; Moller, M. B.; Parsons, B. M.; Van Krieken, J. H.; Piris, M. A.; Winter, J. N.; Li, Y.; Xu, B.; Young, K. H.
Authors of the University:
FERRERI ANDRES JOSE MARIA
PONZONI MAURILIO
Handle:
https://iris.unisr.it/handle/20.500.11768/153120
Full Text:
https://iris.unisr.it//retrieve/handle/20.500.11768/153120/179148/s41408-022-00617-5.pdf
Published in:
BLOOD CANCER JOURNAL
Journal
  • Overview

Overview

URL

https://www.nature.com/articles/s41408-022-00617-5
  • Use of cookies

Powered by VIVO | Designed by Cineca | 26.7.2.0