Evidence map›Paper›PMID 37567953›Full record

ArticleNPJ precision oncology2023

Prevalence and clinico-genomic characteristics of patients with TRK fusion cancer in China.

Yujun Xu, Xiaoliang Shi, Weifeng Wang, Lin Zhang, Shinghu Cheung, Marion Rudolph, Nicoletta Brega, Xiaowei Dong, Lili Qian, Liwei Wang and 3 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Future oncology (London, England) · 2025
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. 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

13 authors at 6 institutions in 5 countries.

Yujun XuDepartment of Imaging Interventional Therapy, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University; Department of Imaging Interventional Therapy, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 250021, Jinan, China.
Xiaoliang ShiOrigiMed Co. Ltd, 201114, Shanghai, China.
Weifeng WangOrigiMed Co. Ltd, 201114, Shanghai, China.
Lin ZhangOrigiMed Co. Ltd, 201114, Shanghai, China.
Shinghu CheungPrecision Molecular Oncology, Research and Early Development - Oncology, Pharmaceuticals, Bayer U.S. LLC, Cambridge, USA.ORCID http://orcid.org/0000-0003-2093-6183
Marion RudolphTranslational Sciences Oncology, Research and Early Development - Oncology, Pharmaceuticals, Bayer AG, Berlin, Germany.
Nicoletta BregaStrategic Business Unit Oncology, Bayer S.p.A, Milan, Italy.ORCID http://orcid.org/0000-0002-5091-4631
Xiaowei DongOrigiMed Co. Ltd, 201114, Shanghai, China.
Lili QianOrigiMed Co. Ltd, 201114, Shanghai, China.
Liwei WangOrigiMed Co. Ltd, 201114, Shanghai, China.
Shaohua YuanOrigiMed Co. Ltd, 201114, Shanghai, China.
Daniel Shao Weng TanNational Cancer Centre Singapore, Duke-NUS Medical School, 169610, Singapore, Singapore. daniel.tan.s.w@singhealth.com.sg.
Kai WangOrigiMed Co. Ltd, 201114, Shanghai, China. wangk@origimed.com.ORCID http://orcid.org/0000-0002-8272-2888
Unimed Medical Institute · CNBayer (Germany) · DEBayer (Italy) · ITBayer (United States) · USShandong University · CNSingHealth · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurotrophic tyrosine kinase (NTRK) fusions involving NTRK1, NTRK2, and NTRK3 were found in a broad range of solid tumors as driver gene variants. However, the prevalence of NTRK fusions in Chinese solid tumor patients is rarely reported. Based on the next-generation sequencing data from 10,194 Chinese solid tumor patients, we identified approximately 0.4% (40/10,194) of Chinese solid tumor patients with NTRK fusion. NTRK fusions were most frequently detected in soft tissue sarcoma (3.0%), especially in the fibrosarcoma subtype (12.7%). A total of 29 NTRK fusion patterns were identified, of which 11 were rarely reported. NTRK fusion mostly co-occurred with TP53 (38%), CDKN2A (23%), and ACVR2A (18%) and rarely with NTRK amplification (5.0%) and single nucleotide variants (2.5%). DNA-based NTRK fusion sequencing exhibited a higher detection rate than pan-TRK immunohistochemistry (100% vs. 87.5%). Two patients with NTRK fusions showed clinical responses to larotrectinib, supporting the effective response of NTRK fusion patients to TRK inhibitors.

Identifiers

PMID37567953
PMCPMC10421940
OpenAlexW4385767312

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.