Pan-TRK Immunohistochemistry: An Example-Based Practical Approach to Efficiently Identify Patients With NTRK Fusion Cancer.


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
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

1031-1040

Déclaration 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.

Auteurs

Esther Conde (E)

From Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, CIBERONC, Madrid, Spain (Conde, Lopez-Rios).

Susana Hernandez (S)

Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, Madrid, Spain (Hernandez, Sanchez, Alonso, Martinez).

Elena Sanchez (E)

Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, Madrid, Spain (Hernandez, Sanchez, Alonso, Martinez).

Rita Maria Regojo (RM)

Pathology, Hospital Universitario La Paz, Madrid, Spain (Regojo).

Carmen Camacho (C)

Pathology, Complejo Hospitalario Universitario Insular Materno-Infantil, Las Palmas de Gran Canaria, Spain (Camacho). Conde and Hernandez contributed equally as co-first authors.

Marta Alonso (M)

Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, Madrid, Spain (Hernandez, Sanchez, Alonso, Martinez).

Rebeca Martinez (R)

Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, Madrid, Spain (Hernandez, Sanchez, Alonso, Martinez).

Fernando Lopez-Rios (F)

From Pathology and Laboratory of Therapeutic Targets, Hospital Universitario HM Sanchinarro, HMHospitales, CIBERONC, Madrid, Spain (Conde, Lopez-Rios).

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Classifications MeSH