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Systematic analysis of off-label and off-guideline cancer therapy usage in a real-world cohort of 165,912 US patients.
Liu, Ruishan; Wang, Lisa; Rizzo, Shemra; Garmhausen, Marius Rene; Pal, Navdeep; Waliany, Sarah; McGough, Sarah; Lin, Yvonne G; Huang, Zhi; Neal, Joel; Copping, Ryan; Zou, James.
Afiliação
  • Liu R; Department of Electrical Engineering, Stanford University, Stanford, CA, USA; Department of Computer Science, University of Southern California, Los Angeles, CA, USA.
  • Wang L; Genentech, South San Francisco, CA, USA.
  • Rizzo S; Genentech, South San Francisco, CA, USA.
  • Garmhausen MR; Genentech, South San Francisco, CA, USA.
  • Pal N; Genentech, South San Francisco, CA, USA.
  • Waliany S; School of Medicine, Stanford University, Stanford, CA, USA.
  • McGough S; Genentech, South San Francisco, CA, USA.
  • Lin YG; Genentech, South San Francisco, CA, USA.
  • Huang Z; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA.
  • Neal J; School of Medicine, Stanford University, Stanford, CA, USA.
  • Copping R; Genentech, South San Francisco, CA, USA. Electronic address: copping.ryan@gene.com.
  • Zou J; Department of Electrical Engineering, Stanford University, Stanford, CA, USA; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA. Electronic address: jamesz@stanford.edu.
Cell Rep Med ; 5(3): 101444, 2024 Mar 19.
Article em En | MEDLINE | ID: mdl-38428426
ABSTRACT
Patients with cancer may be given treatments that are not officially approved (off-label) or recommended by guidelines (off-guideline). Here we present a data science framework to systematically characterize off-label and off-guideline usages using real-world data from de-identified electronic health records (EHR). We analyze treatment patterns in 165,912 US patients with 14 common cancer types. We find that 18.6% and 4.4% of patients have received at least one line of off-label and off-guideline cancer drugs, respectively. Patients with worse performance status, in later lines, or treated at academic hospitals are significantly more likely to receive off-label and off-guideline drugs. To quantify how predictable off-guideline usage is, we developed machine learning models to predict which drug a patient is likely to receive based on their clinical characteristics and previous treatments. Finally, we demonstrate that our systematic analyses generate hypotheses about patients' response to treatments.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Limite: Humans Idioma: En Revista: Cell Rep Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Limite: Humans Idioma: En Revista: Cell Rep Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos