Evidence map›Paper›PMID 37938323›Full record

ArticleVirchows Archiv : an international journal of pathology2023

mTOR eosinophilic renal cell carcinoma: a distinctive tumor characterized by mTOR mutation, loss of chromosome 1, cathepsin-K expression, and response to target therapy.

Anna Caliò, Stefano Marletta, Giulio Settanni, Mimma Rizzo, Stefano Gobbo, Serena Pedron, Lavinia Stefanizzi, Enrico Munari, Matteo Brunelli, Lisa Marcolini and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
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

19 authors at 11 institutions in 2 countries.

Anna Caliò *Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Stefano Marletta *Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Giulio SettanniDepartment of Pathology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar, Italy.
Mimma RizzoDivision of Medical Oncology, A.O.U. Consorziale Policlinico Di Bari, Bari, Italy.
Stefano GobboDepartment of Translational Medicine, University of Ferrara, Ferrara, Italy.
Serena PedronDepartment of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Lavinia StefanizziDepartment of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy.
Enrico MunariDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Matteo BrunelliDepartment of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Lisa MarcoliniDepartment of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy.
Anna PesciDepartment of Pathology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar, Italy.
Stefano FratoniDivision of Anatomic Pathology, S. Eugenio Hospital, Rome, Italy.
Francesco PiercontiDivision of Anatomic Pathology and Histology, Foundation "A. Gemelli" University Hospital, Università Cattolica del Sacro Cuore, Rome, Italy.
Maria Rosaria RaspolliniHistopathology and Molecular Diagnostics, Azienda Ospedaliero Universitaria Careggi, Florence, Italy.
Antonio MarchettiDivision of Anatomic Pathology and Histology, Ospedale Clinicizzato "SS. Annunziata" Università Di Chieti, Chieti, Italy.
Claudio DoglioniDepartment of Pathology, San Raffaele Hospital, Milan, Italy.
Mahul B AminDepartment of Pathology and Laboratory Medicine, University of Tennessee Health Science, Memphis, TN, USA.
Camillo PortaInterdisciplinary Department of Medicine, University of Bari "A. Moro, Bari, Italy.
Guido MartignoniDepartment of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy. guido.martignoni@univr.it.ORCID http://orcid.org/0000-0002-7761-7274
University of Verona · ITCasa di Cura Villa Garda · ITOspedale Sacro Cuore Don Calabria · ITAzienda Ospedaliero-Universitaria Careggi · ITOspedale SS. Annunziata · ITSt. Eugenio Hospital · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Bari Aldo Moro · ITUniversity of Brescia · ITUniversity of Ferrara · ITUniversity of Tennessee Health Science Center · US

Funding

Bando di ricerca finalizzata 2021 GR-2021-12374462
6 · The paper itself

Abstract

In the spectrum of oncocytic renal neoplasms, a subset of tumors with high-grade-appearing histologic features harboring pathogenic mutations in mammalian target of rapamycin (mTOR) and hitherto clinical indolent behavior has been described. Three cases (2F,1 M) with histologically documented metastases (lymph node, skull, and liver) were retrieved and extensively investigated by immunohistochemistry, FISH, and next-generation sequencing. Tumors were composed of eosinophilic cells with prominent nucleoli (G3 by ISUP/WHO) arranged in solid to nested architecture. Additionally, there were larger cells with perinuclear cytoplasmic shrinkage and sparse basophilic Nissl-like granules, superficially resembling the so-called spider cells of cardiac rhabdomyomas. The renal tumors, including the skull and liver metastases, showed immunoexpression PAX8, CK8-18, and cathepsin-K, and negativity for vimentin. NGS identified mTOR genetic alterations in the three cases, including the skull and liver metastases. One patient was then treated with Everolimus (mTOR inhibitors) with clinical response (metastatic tumor shrinkage). We present a distinct renal tumor characterized by high-grade eosinophilic cells, cathepsin-K immunohistochemical expression, and harboring mTOR gene mutations demonstrating a malignant potential and showing responsiveness to mTOR inhibitors.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLiver NeoplasmsBiomarkers, TumorCathepsin KChromosomes, Human, Pair 1HumansMTOR InhibitorsMutationTOR Serine-Threonine KinasesBiomarkers, TumorCathepsin KCTSK protein, humanMTOR InhibitorsMTOR protein, humanTOR Serine-Threonine KinasesCathepsin-KEosinophilic-RCCmTORmTOR inhibitorsNext-generation sequencingOncocyticRCC

Identifiers

PMID37938323
PMCPMC10700445
OpenAlexW4388498514

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.