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Evaluating eligibility criteria of oncology trials using real-world data and AI.
Liu, Ruishan; Rizzo, Shemra; Whipple, Samuel; Pal, Navdeep; Pineda, Arturo Lopez; Lu, Michael; Arnieri, Brandon; Lu, Ying; Capra, William; Copping, Ryan; Zou, James.
Afiliação
  • Liu R; Department of Electrical Engineering, Stanford University, Stanford, CA, USA.
  • Rizzo S; Genentech, South San Francisco, CA, USA.
  • Whipple S; Genentech, South San Francisco, CA, USA.
  • Pal N; Genentech, South San Francisco, CA, USA.
  • Pineda AL; Genentech, South San Francisco, CA, USA.
  • Lu M; Genentech, South San Francisco, CA, USA.
  • Arnieri B; Genentech, South San Francisco, CA, USA.
  • Lu Y; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA.
  • Capra W; Genentech, South San Francisco, CA, USA.
  • Copping R; Genentech, South San Francisco, CA, USA. copping.ryan@gene.com.
  • Zou J; Department of Electrical Engineering, Stanford University, Stanford, CA, USA. jamesz@stanford.edu.
Nature ; 592(7855): 629-633, 2021 04.
Article em En | MEDLINE | ID: mdl-33828294
ABSTRACT
There is a growing focus on making clinical trials more inclusive but the design of trial eligibility criteria remains challenging1-3. Here we systematically evaluate the effect of different eligibility criteria on cancer trial populations and outcomes with real-world data using the computational framework of Trial Pathfinder. We apply Trial Pathfinder to emulate completed trials of advanced non-small-cell lung cancer using data from a nationwide database of electronic health records comprising 61,094 patients with advanced non-small-cell lung cancer. Our analyses reveal that many common criteria, including exclusions based on several laboratory values, had a minimal effect on the trial hazard ratios. When we used a data-driven approach to broaden restrictive criteria, the pool of eligible patients more than doubled on average and the hazard ratio of the overall survival decreased by an average of 0.05. This suggests that many patients who were not eligible under the original trial criteria could potentially benefit from the treatments. We further support our findings through analyses of other types of cancer and patient-safety data from diverse clinical trials. Our data-driven methodology for evaluating eligibility criteria can facilitate the design of more-inclusive trials while maintaining safeguards for patient safety.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Ensaios Clínicos como Assunto / Seleção de Pacientes / Segurança do Paciente / Conjuntos de Dados como Assunto / Oncologia Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inteligência Artificial / Ensaios Clínicos como Assunto / Seleção de Pacientes / Segurança do Paciente / Conjuntos de Dados como Assunto / Oncologia Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article