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Understanding inequities in precision oncology diagnostics.
Dutta, Ritika; Vallurupalli, Mounica; McVeigh, Quinn; Huang, Franklin W; Rebbeck, Timothy R.
Afiliação
  • Dutta R; Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Vallurupalli M; Harvard Medical School, Boston, MA, USA.
  • McVeigh Q; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Huang FW; Cancer Program, Broad Institute, Cambridge, MA, USA.
  • Rebbeck TR; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Nat Cancer ; 4(6): 787-794, 2023 06.
Article em En | MEDLINE | ID: mdl-37248397
ABSTRACT
Advances in molecular diagnostics have enabled the identification of targetable driver pathogenic variants, forming the basis of precision oncology care. However, the adoption of new technologies, such as next-generation sequencing (NGS) panels, can exacerbate healthcare disparities. Here, we summarize data on use patterns of advanced biomarker testing, highlight the disparities in both accessing NGS testing and using this data to match patients to appropriate personalized therapies and propose multidisciplinary strategies to address inequities looking forward.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Aspecto: Equity_inequality Limite: Humans Idioma: En Revista: Nat Cancer Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Aspecto: Equity_inequality Limite: Humans Idioma: En Revista: Nat Cancer Ano de publicação: 2023 Tipo de documento: Article