Evidence map›Paper›PMID 39470841›Full record

ArticleWorld journal of urology2024

Prognostic implications and diagnostic significance of TFE3 rearrangement in renal cell carcinoma.

Carmina Muñoz Bastidas, Mario Tapia Tapia, Andrés Calva López, Vanessa Talavera Cobo, Juan Colombas Vives, Eduardo Miraval Wong, Cristina Gutiérrez Castané, Francisco Javier Ancizu Marckert, Marcos Torres Roca, Luis Labairu Huerta and 6 more

Abstract read
In one paragraph

Article in World journal of urology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Cancers · 2026
    Review
  4. Article
  5. Article
  6. Case Report: ExtrarenalFrontiers in oncology · 2025
    Article
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

16 authors.

Carmina Muñoz BastidasUniversity of Navarra Clinic, Urology, Pamplona, Spain. cmunozbasti@unav.es.ORCID http://orcid.org/0009-0000-1175-5706
Mario Tapia TapiaUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Andrés Calva LópezUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Vanessa Talavera CoboUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Juan Colombas VivesUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Eduardo Miraval WongUniversity of Navarra Clinic, Pathology, Pamplona, Spain.
Cristina Gutiérrez CastanéUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Francisco Javier Ancizu MarckertUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Marcos Torres RocaUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Luis Labairu HuertaUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Fernando Diez-Caballero AlonsoUniversity of Navarra Clinic, Urology, Pamplona, Spain.
José Enrique Robles GarcíaUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Felipe Villacampa AubáUniversity of Navarra Clinic, Urology, Pamplona, Spain.
Daniel González PadillaUniversity of Navarra Clinic, Urology, Madrid, Spain.
Bernardino Miñana LópezUniversity of Navarra Clinic, Urology, Madrid, Spain.
Daniel Sánchez ZalabardoUniversity of Navarra Clinic, Urology, Pamplona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the impact of TFE3 rearrangement, analyzing clinicopathological features that influence renal cell carcinoma (RCC) recurrence, and clarify the role of immunohistochemistry (IHC) staining in diagnosis.

methodsWe screened patients diagnosed of clear cell RCC (ccRCC), fluorescence in situ hybridization (FISH) was performed on all TFE3 positive IHC tumors. Clinicopathological and survival features were collected for analysis.

resultsOut of 695 patients treated for renal tumors, 478 (68.7%) were ccRCC and 22 were suspected of TFE3 rearrangement based on IHC. Subsequent testing revealed 8 (1.15%) were positive in the FISH test (TFE3-rearranged-RCC) and 14 (2.01%) tested negative. No significant differences were noted in general characteristics among the three groups, except for age, TFE3-rearranged-RCC were younger than ccRCC (median age, 49 vs. 58 years, p=0.02). TFE3-rearranged-RCC exhibited a significant higher recurrence rate compared to ccRCC (50% vs 18.8%) and multivariate analysis revealed that TFE3 rearrangement, along with tumor size and metastasis, was an independent prognostic factor for recurrence (HR=4.6; 95% CI 1.1-21.2; p=0.05). Survival analysis demonstrated a significant shorter PFS (progression-free survival) for TFE3-rearranged-RCC compared to ccRCC.

conclusionsTFE3 rearrangement is an independent prognostic factor for recurrence and contributes to a worse PFS, suggesting the necessity of careful follow-up. Diagnosis should be confirmed using FISH due to low specificity of IHC. Further studies are needed to confirm TFE3 IHC staining as a prognostic factor.

Indexed as

Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarcinoma, Renal CellGene RearrangementKidney NeoplasmsAdultAgedFemaleHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisRetrospective StudiesSurvival RateBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsTFE3 protein, humanFluorescence in situ hybridizationPrognosisRenal cell carcinomaTFE3TFE3-rearranged-RCC

Identifiers

PMID39470841
PMCPMC11522134

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.