Colonic Adenocarcinomas Harboring NTRK Fusion Genes: A Clinicopathologic and Molecular Genetic Study of 16 Cases and Review of the Literature
Language English Country United States Media print
Document type Journal Article
Grant support
Z99 CA999999
Intramural NIH HHS - United States
ZIA BC011427
Intramural NIH HHS - United States
PubMed
31567189
PubMed Central
PMC8170835
DOI
10.1097/pas.0000000000001377
PII: 00000478-202002000-00003
Knihovny.cz E-resources
- MeSH
- Adenocarcinoma diagnosis genetics pathology MeSH
- Oncogene Proteins, Fusion genetics metabolism MeSH
- Immunohistochemistry MeSH
- Middle Aged MeSH
- Humans MeSH
- Membrane Glycoproteins genetics metabolism MeSH
- Biomarkers, Tumor genetics metabolism MeSH
- Colonic Neoplasms diagnosis genetics pathology MeSH
- Follow-Up Studies MeSH
- Oncogene Fusion MeSH
- Receptor, trkA genetics metabolism MeSH
- Receptor, trkB genetics metabolism MeSH
- Receptor, trkC genetics metabolism MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Neoplasm Staging MeSH
- Receptor Protein-Tyrosine Kinases genetics metabolism MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Oncogene Proteins, Fusion MeSH
- Membrane Glycoproteins MeSH
- Biomarkers, Tumor MeSH
- Receptor, trkA MeSH
- Receptor, trkB MeSH
- Receptor, trkC MeSH
- tropomyosin-related kinase-B, human MeSH Browser
- Receptor Protein-Tyrosine Kinases MeSH
This study was undertaken to determine the frequency, and the clinicopathologic and genetic features, of colon cancers driven by neurotrophic receptor tyrosine kinase (NTRK) gene fusions. Of the 7008 tumors screened for NTRK expression using a pan-Trk antibody, 16 (0.23%) had Trk immunoreactivity. ArcherDx assay detected TPM3-NTRK1 (n=9), LMNA-NTRK1 (n=3), TPR-NTRK1 (n=2) and EML4-NTRK3 (n=1) fusion transcripts in 15 cases with sufficient RNA quality. Patients were predominantly women (median age: 63 y). The tumors involved the right (n=12) and left colon unequally and were either stage T3 (n=12) or T4. Local lymph node and distant metastases were seen at presentation in 6 and 1 patients, respectively. Lymphovascular invasion was present in all cases. Histologically, tumors showed moderate to poor (n=11) differentiation with a partly or entirely solid pattern (n=5) and mucinous component (n=10), including 1 case with sheets of signet ring cells. DNA mismatch repair-deficient phenotype was seen in 13 cases. Tumor-infiltrating CD4/CD8 lymphocytes were prominent in 9 cases. Programmed death-ligand 1 positive tumor-infiltrating immune cells and focal tumor cell positivity were seen in the majority of cases. CDX2 expression and loss of CK20 and MUC2 expression were frequent. CK7 was expressed in 5 cases. No mutations in BRAF, RAS, and PIK3CA were identified. However, other genes of the PI3K-AKT/MTOR pathway were mutated. In several cases, components of Wnt/β-catenin (APC, AMER1, CTNNB1), p53, and TGFβ (ACVR2A, TGFBR2) pathways were mutated. However, no SMAD4 mutations were found. Two tumors harbored FBXW7 tumor suppressor gene mutations. NTRK fusion tumors constitute a distinct but rare subgroup of colorectal carcinomas.
Department of Clinical Pathomorphology Medical University of Lublin Lublin
Department of Medical Surgical and Health Sciences University of Trieste Trieste
Department of Pathology Aichi Medical University School of Medicine Nagakute Japan
Department of Pathology and Laboratory Medicine Milan Italy
Department of Pathology Central Clinical Hospital of the Ministry of Interior
Department of Pathomorphology Copernicus Hospital Gdańsk Gdańsk
Department of Pathomorphology Jagiellonian University
Department of Pathomorphology Provincial Hospital Gorzów Wielkopolski
Department of Pathomorphology Provincial Hospital Olsztyn
Department of Surgery University of Helsinki
Department of Tumor Pathology Centre of Oncology Maria Skłodowska Curie Memorial Institute Kraków
Departments of Biology and Genetics
Departments of Molecular Diagnostics
Diagnostic Histopathology Laboratory Opole
Division of Pathology National Cancer Institute Aviano
Division of Pathomorphology and Oncological Cytology Wrocław Medical University Wrocław
Faculty of Health Sciences Jan Kochanowski University Kielce
Health Sciences and Physical Education University of Technology and Humanities Radom
Independent Laboratory of Pathology Zdunomed Szczecin
Institute of Pathology University Hospital of Erlangen Erlangen Germany
Laboratory of Pathology ElPat Elbląg Poland
Laboratory of Pathology National Cancer Institute Bethesda MD
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