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Updated: Nov 14, 2025

A Genetically Engineered Mouse Model of Sporadic Colorectal Cancer
Published on: July 6, 2017
NTRK fusion in Japanese colorectal adenocarcinomas
Yuya Yamashiro1, Taisei Kurihara1,2, Takuo Hayashi1
1Department of Human Pathology, Juntendo University School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo, Japan.
Abstract:
NTRK fusion-positive tumors are known to be highly sensitive to TRK inhibitors, such as larotrectinib and entrectinib. Therefore, identification of patients who can potentially benefit from these inhibitors is important; however, the frequency of NTRK fusions in Japanese patients with colorectal cancer (CRC) is unknown. We performed pan-TRK staining using TMA-based immunohistochemistry (IHC) on samples from 971 consecutive Japanese CRC cases from a single institution. Positive cases were further analyzed using NanoString and subsequent targeted RNA sequencing. We found three positive cases using TRK-IHC. Furthermore, the Nanostring assay supported the presence of NTRK fusion in these cases. Subsequent targeted RNA-sequencing and RT-PCR revealed two cases with TPM3-NTRK1 and one with TPR-NTRK1. The TNM stages of these cases were stage I, stage IIA, and stage IIIB, and two showed microsatellite instability-high status. Next-generation sequencing analysis using Cancer hotspot panel revealed TP53 and SMAD4 mutations in separate cases. IHC of β-catenin did not show nuclear accumulation. We found three cases (0.31%) of CRC with NTRK1 fusion among 971 consecutive Japanese CRC cases. No potential driver alterations other than NTRK fusion were identified in these three patients.
Insights
This study investigated NTRK fusions in Japanese colorectal cancer (CRC) patients. Three NTRK1 fusions were identified, suggesting a potential target for TRK inhibitors in a subset of CRC cases.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- NTRK fusion-positive tumors show sensitivity to TRK inhibitors like larotrectinib and entrectinib.
- Identifying patients for TRK inhibitor therapy is crucial.
- The frequency of NTRK fusions in Japanese colorectal cancer (CRC) is not well-established.
Purpose of the Study:
- To determine the frequency of NTRK fusions in Japanese patients with colorectal cancer.
- To characterize the identified NTRK fusions and associated genetic alterations.
Main Methods:
- Pan-TRK immunohistochemistry (IHC) on 971 Japanese CRC cases.
- NanoString assay and targeted RNA sequencing for fusion confirmation.
- RT-PCR and next-generation sequencing for genetic analysis.
Main Results:
- Three cases (0.31%) of NTRK1 fusions were identified in Japanese CRC patients.
- TPM3-NTRK1 and TPR-NTRK1 fusions were detected.
- Associated mutations included TP53 and SMAD4; two cases were microsatellite instability-high.
Conclusions:
- NTRK1 fusions occur at a low frequency in Japanese CRC.
- These fusions represent a potential actionable target for TRK inhibitors in this patient population.
- No other driver alterations were found in the fusion-positive cases.
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