Evidence map›Paper›PMID 30249036›Full record

ReviewBioengineering (Basel, Switzerland)2018

Embryonal Tumors of the Central Nervous System in Children: The Era of Targeted Therapeutics.

David E Kram, Jacob J Henderson, Muhammad Baig, Diya Chakraborty, Morgan A Gardner, Subhasree Biswas, Soumen Khatua

Open access · goldAbstract readReview
In one paragraph

Review in Bioengineering (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Primary Intracranial High Grade Congenital Glial Lesions (PIHGCL): A systematic review of case reports from 1985 to 2025.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Intracranial Tumors in the First Year of Life.Advances and technical standards in neurosurgery · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Childhood medulloblastoma-a single institution's historical perspective on survival and functional morbidity.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Article
  16. Introduction to the Special Issue on Pediatric Neuro-Oncology.Bioengineering (Basel, Switzerland) · 2018
    Article
  17. 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

7 authors at 4 institutions in 2 countries.

David E KramSection of Pediatric Hematology-Oncology, Department of Pediatrics, Wake Forest School of Medicine, Winston Salem, NC 27157, USA. dkram@wakehealth.edu.
Jacob J HendersonPape Family Pediatric Research Institute, Department of Pediatrics, Oregon Health and Science University, Portland, OR 97239, USA. hendejac@ohsu.edu.ORCID 0000-0002-3465-2256
Muhammad BaigDepartment of Pediatrics, MD Anderson Cancer Center, Houston, TX 77030, USA. MBaig@mdanderson.org.
Diya ChakrabortyDepartment of Pediatrics, MD Anderson Cancer Center, Houston, TX 77030, USA. DChakraborty@mdanderson.org.
Morgan A GardnerDepartment of Pediatrics, Wake Forest School of Medicine, Winston Salem, NC 27157, USA. magardne@wakehealth.edu.
Subhasree BiswasDepartment of Pediatrics, MD Anderson Cancer Center, Houston, TX 77030, USA. subhabis@gmail.com.
Soumen KhatuaDepartment of Pediatrics, MD Anderson Cancer Center, Houston, TX 77030, USA. SKhatua@mdanderson.org.ORCID 0000-0001-6416-650X
The University of Texas MD Anderson Cancer Center · USWake Forest University · USHumanitas University · ITOregon Health & Science University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Embryonal tumors (ET) of the central nervous system (CNS) in children encompass a wide clinical spectrum of aggressive malignancies. Until recently, the overlapping morphological features of these lesions posed a diagnostic challenge and undermined discovery of optimal treatment strategies. However, with the advances in genomic technology and the outpouring of biological data over the last decade, clear insights into the molecular heterogeneity of these tumors are now well delineated. The major subtypes of ETs of the CNS in children include medulloblastoma, atypical teratoid rhabdoid tumor (ATRT), and embryonal tumors with multilayered rosettes (ETMR), which are now biologically and clinically characterized as different entities. These important developments have paved the way for treatments guided by risk stratification as well as novel targeted therapies in efforts to improve survival and reduce treatment burden.

Indexed as

ATRTcentral nervous systemchildrenembryonal tumorsETMRmedulloblastomamolecular biologytargeted therapeutics

Identifiers

PMID30249036
PMCPMC6315657
OpenAlexW2889585165

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.