Evidence map›Paper›PMID 26373296›Full record

ReviewJournal of neuro-oncology2016

Evaluation of the good tumor response of embryonal tumor with abundant neuropil and true rosettes (ETANTR).

Petra Mozes, Péter Hauser, Tibor Hortobágyi, Gábor Benyó, István Peták, Miklós Garami, Adrienne Cserháti, Katalin Bartyik, László Bognár, Zoltán Nagy and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Extracranial extra-CNS spread of embryonal tumor with multilayered rosettes (ETMR): case series and systematic review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Embryonal tumor with multilayered rosettes: illustrative case and review of the literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Review
  6. 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

12 authors at 4 institutions in 1 country.

Petra MozesDepartment of Oncotherapy, Faculty of Medicine, University of Szeged, Szeged, Hungary. mozespetra@gmail.com.
Péter Hauser2nd Department of Paediatrics, Semmelweis University, Budapest, Hungary.
Tibor HortobágyiDepartment of Pathology, Medical Center, University of Debrecen, Debrecen, Hungary.
Gábor BenyóPaediatric Haematology and Stem Cell Transplantation Unit, St. István and St. László Hospital, Budapest, Hungary.
István PetákMTA-SE Pathobiochemistry Research Group, Department of Medical Chemistry, Semmelweis University, Budapest, Hungary.
Miklós Garami2nd Department of Paediatrics, Semmelweis University, Budapest, Hungary.
Adrienne CserhátiDepartment of Oncotherapy, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Katalin BartyikDepartment of Paediatrics and Paediatric Health Care Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.
László BognárDepartment of Neurosurgery, Medical Center, University of Debrecen, Debrecen, Hungary.
Zoltán NagyDepartment of Oncotherapy, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Eszter Turányi1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Katalin HideghétyDepartment of Oncotherapy, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Semmelweis University · HUUniversity of Szeged · HUUniversity of Debrecen · HUUnified Szent István and Szent László Hospital · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The embryonal tumor with abundant neuropil and true rosettes is a rare and highly malignant variant of embryonal brain tumors. It usually affects infants and young children under the age of 4 years and exhibits a very aggressive course with a dismal prognosis. For the 68 cases reported to date the mean age at diagnosis was 25.42 months (range 3-57 months). Survival data are available for 48 children (including our case): the median overall survival is 13.0 months, though 6 (9%) of the children have had a relative long survival (>30 months). The aggressive combined treatment, involving primary surgical tumor removal, adjuvant polychemotherapy, including high-dose chemotherapy with stem cell transplantation, radiotherapy and radiochemotherapy, might play an important role in the longer survival. We have performed a literature review and we present here a multimodal-treated case of a 2- year-old girl with a long survival, who was reoperated when recurrence occurred. The residual tumor demonstrated a good response to temozolomide radiochemotherapy (craniospinal axis + boost) and followed by maintenance temozolomide. The described complex aggressive treatment option might be considered for future cases of this tumor entity.

Indexed as

Brain NeoplasmsChild, PreschoolFemaleHumansKi-67 AntigenMagnetic Resonance ImagingNeoplasms, Germ Cell and EmbryonalNeuropilKi-67 AntigenCraniospinal axisETANTRRadiochemotherapyTemozolomide

Identifiers

PMID26373296
OpenAlexW1685821459

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.