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BRAF mutant appendiceal adenocarcinoma differs from colorectal cancer but responds to BRAF-targeted therapy

  • Vinay K. Pattalachinti
  • , Emaan Haque
  • , Mahmoud Yousef
  • , Abdelrahman Yousef
  • , Saikat Chowdhury
  • , Michael Overman
  • , Christine M. Parseghian
  • , Van K. Morris
  • , Bryan Kee
  • , Ryan W. Huey
  • , Kanwal Raghav
  • , Colin M. Court
  • , John Paul Shen

Producción científica: Articlerevisión exhaustiva

Resumen

Appendiceal Adenocarcinoma (AA) is a rare gastrointestinal cancer with no FDA-approved targeted therapies. Here, we retrospectively compare BRAF-mutant AA and colorectal cancer (CRC). BRAF mutation is rare in AA (3%). Unlike CRC, BRAFV600E AA is not associated with poor prognosis, female sex, microsatellite instability, mucinous histology, or poor differentiation. In both cancers, BRAFV600E but not atypical BRAF mutations are mutually exclusive with other Ras-activating mutations. BRAFV600E + EGFR inhibition shows efficacy in BRAFV600E AA (disease control rate = 80%, median progression-free survival = 7.1 months).

Idioma originalEnglish (US)
Número de artículo38
Publicaciónnpj Precision Oncology
Volumen9
N.º1
DOI
EstadoPublished - dic 2025
Publicado de forma externa

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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