Evidence map›Paper›PMID 39409115›Full record

ArticleInternational journal of molecular sciences2024

Descriptive Analysis of Common Fusion Mutations in Papillary Thyroid Carcinoma in Hungary.

Richard Armos, Bence Bojtor, Janos Podani, Ildiko Illyes, Bernadett Balla, Zsuzsanna Putz, Andras Kiss, Andrea Kohanka, Erika Toth, Istvan Takacs and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Molecular and clinicopathological characteristics ofHistology and histopathology · 2026
    Review
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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

12 authors.

Richard ArmosDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.ORCID 0009-0005-3334-1308
Bence BojtorDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.ORCID 0009-0004-5018-751X
Janos PodaniDepartment of Plant Systematics, Ecology and Theoretical Biology, Eötvös Loránd University, 1117 Budapest, Hungary.
Ildiko IllyesDepartment of Pathology, Forensic and Insurance Medicine, Faculty of Medicine, Semmelweis University, 1091 Budapest, Hungary.
Bernadett BallaSE HUN-REN-TKI ENDOMOLPAT Research Group, 1085 Budapest, Hungary.
Zsuzsanna PutzDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Andras KissDepartment of Pathology, Forensic and Insurance Medicine, Faculty of Medicine, Semmelweis University, 1091 Budapest, Hungary.ORCID 0000-0002-7453-3163
Andrea KohankaDepartment of Surgical and Molecular Pathology, National Institute of Oncology, 1122 Budapest, Hungary.ORCID 0000-0001-8834-4657
Erika TothDepartment of Surgical and Molecular Pathology, National Institute of Oncology, 1122 Budapest, Hungary.ORCID 0000-0003-2054-8447
Istvan TakacsDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Janos P KosaDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.
Peter LakatosDepartment of Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1083 Budapest, Hungary.

Funding

Hungarian Research Network SE HUN-REN-TKI ENDOMOLPATMinistry for Innovation and Technology 2020-4.1.1.-TKP2020-MOLORKIV
6 · The paper itself

Abstract

Thyroid cancer is the most common type of endocrine malignancy. Papillary thyroid carcinoma (PTC) is its predominant subtype, which is responsible for the vast majority of cases. It is true that PTC is a malignant tumor with a very good prognosis due to effective primary therapeutic approaches such as thyroidectomy and radioiodine (RAI) therapy. However, we are often required to indicate second-line treatments to eradicate the tumor properly. In these scenarios, molecular therapies are promising alternatives, especially if specifically targetable mutations are present. Many of these targetable gene alterations originate from gene fusions, which can be found using molecular diagnostics like next-generation sequencing (NGS). Nonetheless, molecular profiling is far from being a routine procedure in the initial phase of PTC diagnostics. As a result, the mutation status, except for

Indexed as

MutationThyroid Cancer, PapillaryThyroid NeoplasmsAdultAgedFemaleGene FusionHumansHungaryMaleMiddle AgedOncogene Proteins, FusionRetrospective StudiesOncogene Proteins, Fusionclinicopathological associationsfusion mutationsgene fusionsmolecular diagnosticspapillary thyroid carcinomathyroid cancer

Identifiers

PMID39409115
PMCPMC11477448

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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.