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Topological Structures in the Space of Treatment-Naïve Patients with Chronic Lymphocytic Leukemia.
McGee, Reginald L; Reed, Jake; Coombes, Caitlin E; Herling, Carmen D; Keating, Michael J; Abruzzo, Lynne V; Coombes, Kevin R.
Afiliación
  • McGee RL; Department of Mathematics and Statistics, Haverford College, Haverford, PA 19041, USA.
  • Reed J; Department of Biostatistics, Data Science, and Epidemiology, Georgia Cancer Center at Augusta University, Augusta, GA 30912, USA.
  • Coombes CE; Department of Anesthesiology, Stanford University, Palo Alto, CA 94305, USA.
  • Herling CD; Clinic of Hematology, Cellular Therapy, Hemostaseology, and Infectious Diseases, University of Leipzig, 04103 Leipzig, Germany.
  • Keating MJ; Department of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
  • Abruzzo LV; Department of Pathology, Medical University of South Carolina, Charleston, SC 29425, USA.
  • Coombes KR; Department of Biostatistics, Data Science, and Epidemiology, Georgia Cancer Center at Augusta University, Augusta, GA 30912, USA.
Cancers (Basel) ; 16(15)2024 Jul 26.
Article en En | MEDLINE | ID: mdl-39123390
ABSTRACT
Patients are complex and heterogeneous; clinical data sets are complicated by noise, missing data, and the presence of mixed-type data. Using such data sets requires understanding the high-dimensional "space of patients", composed of all measurements that define all relevant phenotypes. The current state-of-the-art merely defines spatial groupings of patients using cluster analyses. Our goal is to apply topological data analysis (TDA), a new unsupervised technique, to obtain a more complete understanding of patient space. We applied TDA to a space of 266 previously untreated patients with Chronic Lymphocytic Leukemia (CLL), using the "daisy" metric to compute distances between clinical records. We found clear evidence for both loops and voids in the CLL data. To interpret these structures, we developed novel computational and graphical methods. The most persistent loop and the most persistent void can be explained using three dichotomized, prognostically important factors in CLL IGHV somatic mutation status, beta-2 microglobulin, and Rai stage. In conclusion, patient space turns out to be richer and more complex than current models suggest. TDA could become a powerful tool in a researcher's arsenal for interpreting high-dimensional data by providing novel insights into biological processes and improving our understanding of clinical and biological data sets.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza