Evidence map›Paper›PMID 35506567›Full record

ArticleCancer medicine2022

NTRK fusion positive colorectal cancer is a unique subset of CRC with high TMB and microsatellite instability.

Hui Wang, Zhi-Wei Li, Qiuxiang Ou, Xue Wu, Misako Nagasaka, Yang Shao, Sai-Hong Ignatius Ou, Yu Yang

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
9.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 65 citations in OpenAlex.

  1. Annals of medicine and surgery (2012) · 2026
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  6. World journal of gastrointestinal oncology · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Current Status of Precision Medicine in Colorectal Cancer in Japan.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Article
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  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Hui WangDepartment of Medical Oncology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, China.
Zhi-Wei LiDepartment of Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, China.
Qiuxiang OuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.ORCID 0000-0002-2961-2057
Xue WuGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.
Misako NagasakaKarmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.ORCID 0000-0001-5308-615X
Yang ShaoGeneseeq Research Institute, Nanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.
Sai-Hong Ignatius OuChao Family Comprehensive Cancer Center, University of California Irvine School of Medicine, Orange, California, USA.ORCID 0000-0002-1764-4975
Yu YangDepartment of Oncology, the Second Affiliated Hospital of Harbin Medical University, Harbin Medical University, Harbin, China.
Genesee Community College · USHarbin Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNNanjing Medical University · CNUniversity of California, Irvine · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TRK fusions are rare but targetable mutations which occur across a wide variety of cancer types. We report the prevalence of approximately 0.7% for NTRK-positive colorectal cancer (CRC) by genetically profiling 2519 colonic and rectal tumors. The aberrations of APC and TP53 frequently co-occurred with NTRK gene fusions, whereas RAS/BRAF oncogenic alterations and NTRK fusions were almost always mutually exclusive. NTRK-driven colorectal cancer patients demonstrated increased TMB (median = 53 mut/MB, 95% CI: 36.8-68.0 mut/MB), high microsatellite instability, and an enrichment for POLE/POLD1 mutations when compared to molecularly unstratified colorectal cancer population. These data shed light on possible future approach of multimodality treatment regimen including TRK-targeted therapy and immune checkpoint inhibitor therapy in NTRK-positive CRCs.

Indexed as

Colorectal NeoplasmsMicrosatellite InstabilityGene FusionHumansMutationcolorectal cancergene fusionsmicrosatellite instabilityNTRKPOLE/POLD1tumor mutation burden

Identifiers

PMID35506567
PMCPMC9249987
OpenAlexW4225371124

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.