Evidence map›Paper›PMID 27184492›Full record

ReviewTargeted oncology2016

Will Testicular Germ Cell Tumors Remain Untargetable?

Fouad Aoun, Hampig Raphael Kourie, Simone Albisinni, Thierry Roumeguère

Abstract readReview
PubMed Publisher
In one paragraph

Review in Targeted oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. mJournal of translational medicine · 2019
    Article
  2. Article
  3. 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

4 authors at 3 institutions in 2 countries.

Fouad AounDepartment of Urology, Hôtel Dieu de France, Beyrouth, Lebanon. fouad.aoun@bordet.be.
Hampig Raphael KourieDepartment of Oncology, Jules Bordet Institute, 1 Héger Bordet Street, 1000, Brussels, Belgium.
Simone AlbisinniDepartment of Urology, Erasme Hospital, Route de Lennik 808, 1070, Brussels, Belgium.
Thierry RoumeguèreDepartment of Urology, Erasme Hospital, Route de Lennik 808, 1070, Brussels, Belgium.
Erasmus Hospital · BEHôtel-Dieu de France · LBInstitut Jules Bordet · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Testicular Germ cell tumors (TGCT) represent the most common solid tumors affecting young men. They constitute a distinct entity because of their embryonic origin and their unique biological behavior. Recently, new preclinical data on genetic and epigenetic susceptibility profiles, biological signaling machinery as well as on molecular patterns of tumors and pathways of pathogenesis helped to elucidate the pathogenesis and the differentiation of TGCTs and to understand the mechanisms behind the development of resistance to treatment. In the present work, we have reviewed new clues to the development, differentiation and progression of TGCTs. We focus on the most important epigenetic and molecular biomarkers, and discussed their diagnostic and prognostic accuracy compared to the currently used biomarkers. The mechanisms underlying the development of resistance to cisplatin and commonly used chemotherapeutic agents are also discussed in detail. Finally, we summarize failed and ongoing clinical trials using targeted therapies in resistant TGCTs, and analyze the potential of new targeted therapies.

Indexed as

Antineoplastic AgentsHumansNeoplasms, Germ Cell and EmbryonalTesticular NeoplasmsAntineoplastic Agents

Identifiers

PMID27184492
OpenAlexW2406949811

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.