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Natural Language Processing for the Accurate Identification of Colorectal Cancer Mismatch Repair Status in Lynch Syndrome Screening.
Li, Dan; Udaltsova, Natalia; Layefsky, Evan; Doan, Cecilia; Corley, Douglas A.
Afiliação
  • Li D; Department of Gastroenterology, Kaiser Permanente Medical Center, Santa Clara, California; Division of Research, Kaiser Permanente Northern California, Oakland, California. Electronic address: Dan.X.Li@kp.org.
  • Udaltsova N; Division of Research, Kaiser Permanente Northern California, Oakland, California.
  • Layefsky E; Division of Research, Kaiser Permanente Northern California, Oakland, California.
  • Doan C; Division of Research, Kaiser Permanente Northern California, Oakland, California.
  • Corley DA; Division of Research, Kaiser Permanente Northern California, Oakland, California; Department of Gastroenterology, Kaiser Permanente Medical Center, San Francisco, California.
Clin Gastroenterol Hepatol ; 19(3): 610-612.e1, 2021 03.
Article em En | MEDLINE | ID: mdl-32036042
ABSTRACT
Lynch syndrome (LS) is the most common type of hereditary colorectal cancer (CRC) syndrome caused by pathogenic variants in mismatch repair (MMR) genes.1 Current multisociety guidelines recommend screening all CRC tumors for LS.2,3 The most widely adopted screening method is MMR immunohistochemistry (IHC) followed by germline analysis if indicated.2,3 However, the text-based nature of pathology and IHC reports used for LS screening results impedes creation of an efficient tracking system for identifying affected patients and screening outcomes.4 In this study, we developed and validated a natural language processing (NLP) tool for extracting MMR IHC results in LS screening in a large, diverse, multicenter, community-based setting.5.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Idioma: En Ano de publicação: 2021 Tipo de documento: Article