Literature DB >> 26486743

Utility of BRAF V600E mutation-specific immunohistochemistry in detecting BRAF V600E-mutated gastrointestinal stromal tumors.

Deepa T Patil1, Shuang Ma2, Mai Konishi3, Paula D Carver2, Marina Pukay4, Carol Beadling4, Christopher L Corless4, Brian P Rubin2.   

Abstract

OBJECTIVES: As patients with BRAF V600E mutation respond to BRAF inhibitors, it is important to identify these mutations to stratify patients for the appropriate therapy. In this study, we evaluated the utility of a BRAF V600E allele-specific antibody in gastrointestinal stromal tumors (GISTs).
METHODS: BRAF V600E mutation-specific immunohistochemistry (negative, weak, or moderate/strong expression) and BRAF sequencing were performed on 38 consecutive GISTs diagnosed between January 2013 and April 2014.
RESULTS: GISTs from a cohort of 25 men and 13 women (mean age, 61 years; range, 39-88 years) were localized to the stomach (18), small bowel (10), colon (three), rectum (two), and pelvis/omentum (five). Strong and diffuse cytoplasmic BRAF expression was noted in two (5%) of 38 cases, while eight (21%) of 38 cases showed weak staining, and 28 (74%) of 38 cases were negative. Both of the strongly positive cases arose in the stomach, occurring in a 42-year-old and a 47-year-old woman, respectively. The lesions measured 0.8 and 1 cm, showed spindle cell morphology, and had no risk of progressive disease by Miettinen criteria. Both cases showed heterozygous BRAF V600E, while no BRAF mutations were detected in cases with weak or negative BRAF expression.
CONCLUSIONS: BRAF V600E mutation-specific immunohistochemistry is a highly sensitive and specific method for detecting BRAF-mutated GISTs. Copyright© by the American Society for Clinical Pathology.

Entities:  

Keywords:  BRAF V600E; Gastrointestinal stromal tumor; Immunohistochemistry

Mesh:

Substances:

Year:  2015        PMID: 26486743     DOI: 10.1309/AJCPRK3V2EIIUPQZ

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  4 in total

1.  Neurofibromin C terminus-specific antibody (clone NFC) is a valuable tool for the identification of NF1-inactivated GISTs.

Authors:  Sabrina Rossi; Daniela Gasparotto; Matilde Cacciatore; Marta Sbaraglia; Alessia Mondello; Maurizio Polano; Alessandra Mandolesi; Alessandro Gronchi; David E Reuss; Andreas von Deimling; Roberta Maestro; Angelo Paolo Dei Tos
Journal:  Mod Pathol       Date:  2017-09-01       Impact factor: 7.842

2.  Gastrointestinal stromal tumors (GISTs): SEAP-SEOM consensus on pathologic and molecular diagnosis.

Authors:  J Martin-Broto; V Martinez-Marín; C Serrano; N Hindi; J A López-Guerrero; R Ramos-Asensio; A Vallejo-Benítez; D Marcilla-Plaza; R González-Cámpora
Journal:  Clin Transl Oncol       Date:  2016-12-09       Impact factor: 3.405

3.  Analysis of C-Kit Exon 9, Exon 11 and BRAFV600E Mutations Using Sangers Sequencing in Gastrointestinal Stromal Tumours.

Authors:  Divya Madhala; Sandhya Sundaram; MohanaPriya Chinambedudandapani; Archana Balasubramanian
Journal:  Cureus       Date:  2020-03-22

4.  Concomitant KIT/BRAF and PDGFRA/BRAF mutations are rare events in gastrointestinal stromal tumors.

Authors:  Sabrina Rossi; Marta Sbaraglia; Marta Campo Dell'Orto; Daniela Gasparotto; Matilde Cacciatore; Elena Boscato; Valentina Carraro; Luisa Toffolatti; Giovanna Gallina; Monia Niero; Emanuela Pilozzi; Alessandra Mandolesi; Fausto Sessa; Aurelio Sonzogni; Cristina Mancini; Guido Mazzoleni; Salvatore Romeo; Roberta Maestro; Angelo P Dei Tos
Journal:  Oncotarget       Date:  2016-05-24
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.