Pan-TRK Immunohistochemistry: An Example-Based Practical Approach to Efficiently Identify Patients With NTRK Fusion Cancer.
Biomarkers, Tumor
/ genetics
Gene Fusion
Genetic Predisposition to Disease
High-Throughput Nucleotide Sequencing
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Membrane Glycoproteins
/ genetics
Neoplasms
/ genetics
Phenotype
Predictive Value of Tests
Prognosis
Receptor, trkA
/ genetics
Receptor, trkB
/ genetics
Receptor, trkC
/ genetics
Reverse Transcriptase Polymerase Chain Reaction
Journal
Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091
Informations de publication
Date de publication:
01 08 2021
01 08 2021
Historique:
accepted:
20
08
2020
pubmed:
29
10
2020
medline:
14
9
2021
entrez:
28
10
2020
Statut:
ppublish
Résumé
Food and Drug Administration-approved TRK inhibitors with impressive overall response rates are now available for patients with multiple cancer types that harbor NTRK rearrangements, yet the identification of NTRK fusions remains a difficult challenge. These alterations are highly recurrent in extremely rare malignancies or can be detected in exceedingly small subsets of common tumor types. A 2-step approach has been proposed, involving a screening by immunohistochemistry (IHC) followed by a confirmatory method (fluorescence in situ hybridization, reverse transcriptase-polymerase chain reaction, or next-generation sequencing) in cases expressing the protein. However, there is no interpretation guide for any of the available IHC clones. To provide a pragmatic update on the use of pan-TRK IHC. Selected examples of the different IHC staining patterns across multiple histologies are shown. Primary literature review with PubMed, combined with personal diagnostic and research experience. In-depth knowledge of pan-TRK IHC will help pathologists implement a rational approach to the detection of NTRK fusions in human malignancies.
Identifiants
pubmed: 33112951
pii: 446878
doi: 10.5858/arpa.2020-0400-RA
doi:
Substances chimiques
Biomarkers, Tumor
0
Membrane Glycoproteins
0
NTRK1 protein, human
0
NTRK3 protein, human
0
Receptor, trkA
EC 2.7.10.1
Receptor, trkB
EC 2.7.10.1
Receptor, trkC
EC 2.7.10.1
tropomyosin-related kinase-B, human
EC 2.7.10.1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1031-1040Déclaration de conflit d'intérêts
Conde receives honoraria from Roche and Pfizer; travel expenses were covered by Roche, Pfizer, and Merck Sharp & Dohme. Lopez-Rios received honoraria from Lilly, Roche, Thermo Fischer Scientific, Pfizer, Bristol-Myers Squibb, Bayer, AstraZeneca, Merck Sharp & Dohme; research funding was received from Lilly, Roche, and Thermo Fischer Scientific. The other authors have no relevant financial interest in the products or companies described in this article.