Evidence map›Paper›PMID 29858701›Full record

ReviewWorld journal of urology2019

Epidemiology, biology and treatment of sarcomatoid RCC: current state of the art.

Cedric Lebacle, Aydin Pooli, Thomas Bessede, Jacques Irani, Allan J Pantuck, Alexandra Drakaki

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of urology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
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  8. Diagnostic and prognostic role ofEJNMMI research · 2025
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  11. Review
  12. Article
  13. Article
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  15. Article
  16. Molecular mechanisms of resistance to tyrosine kinase inhibitor in clear cell renal cell carcinoma.International journal of urology : official journal of the Japanese Urological Association · 2022
    Review
  17. Article
  18. Review
  19. Effects ofThe Journal of international medical research · 2022
    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

6 authors at 3 institutions in 2 countries.

Cedric LebacleInstitute of Urologic Oncology (IUO), David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. clebacle@mednet.ucla.edu.ORCID http://orcid.org/0000-0002-8215-2918
Aydin PooliDepartment of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Thomas BessedeDepartment of Urology, University Hospital Bicetre, APHP, Le Kremlin Bicetre, France.
Jacques IraniDepartment of Urology, University Hospital Bicetre, APHP, Le Kremlin Bicetre, France.
Allan J PantuckDepartment of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Alexandra DrakakiInstitute of Urologic Oncology (IUO), David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
University of California, Los Angeles · USBicêtre Hospital · FRUCLA Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long recognized to confer an extremely poor prognosis, sarcomatoid dedifferentiation of renal cell carcinoma (sRCC) is a tumor phenotype that is finally beginning to be better understood on the molecular and genetic levels. With an overall incidence that ranges from 1 to 32% depending on associated RCC subtype, the survival of sarcomatoid RCC patients rarely exceeds 2 years. The main reasons for its poor outcome include its aggressive biology, its tendency to present at an advanced or metastatic stage at the time of diagnosis, its high rate of tumor recurrence after nephrectomy, and its limited response to systemic therapies. Molecular pathology studies suggest that sarcomatoid dedifferentiation originates from a focal epithelial-mesenchymal transition (EMT) arising in the carcinomatous component of the tumor. It is hoped that the growing understanding of the molecular biology of sRCC will soon make it possible to adapt treatments based on the identification of actionable tumor alterations. The deliberate inclusion of these patients in the multicenter clinical trials of immune, targeted and combination therapies is a necessary next step in pioneering future treatment strategies.

Indexed as

Antineoplastic AgentsAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellChemotherapy, AdjuvantEpithelial-Mesenchymal TransitionHumansKidney NeoplasmsNeoplasm Recurrence, LocalNephrectomyPrognosisSunitinibSurvival RateAntineoplastic AgentsAntineoplastic Agents, ImmunologicalSunitinibImmunotherapyKidney neoplasmsSarcomatoid renal cell carcinoma

Identifiers

PMID29858701
OpenAlexW2806746916

What OpenQuestion holds

Textmetadata
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.