Evidence map›Paper›PMID 32937871›Full record

ArticleCancers2020

Pediatric Suprasellar Germ Cell Tumors: A Clinical and Radiographic Review of Solitary vs. Bifocal Tumors and Its Therapeutic Implications.

Darian R Esfahani, Tord Alden, Arthur DiPatri, Guifa Xi, Stewart Goldman, Tadanori Tomita

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Pediatric sellar teratoma - Case report and review of the literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Intracranial bifocal germinoma.Radiology case reports · 2022
    Article
  18. Article
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Darian R EsfahaniDivision of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.ORCID 0000-0003-1073-1387
Tord AldenDivision of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.
Arthur DiPatriDivision of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.
Guifa XiDivision of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.
Stewart GoldmanDivision of Hematology, Oncology, Neuro-Oncology & Stem Cell Transplantation, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.
Tadanori TomitaDivision of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital, Chicago, IL 60611, USA.
Northwestern University · USLurie Children's Hospital · US

Funding

Charles and Eleanor Clarke Pediatric Neurosurgery Fellowship n/aYeager Professorship of Pediatric Neurosurgery n/a, Endowment
6 · The paper itself

Abstract

Suprasellar germ cell tumors (S-GCTs) are rare, presenting in either solitary or multifocal fashion. In this study, we retrospectively examine 22 solitary S-GCTs and 20 bifocal germ cell tumors (GCTs) over a 30-year period and demonstrate clinical, radiographic, and prognostic differences between the two groups with therapeutic implications. Compared to S-GCTs, bifocal tumors were almost exclusively male, exhibited higher rate of metastasis, and had worse rates of progression free and overall survival trending toward significance. We also introduce a novel magnetic resonance (MR) imaging classification of suprasellar GCT into five types: a IIIrd ventricle floor tumor extending dorsally with or without an identifiable pituitary stalk (Type Ia, Ib), ventrally (Type III), in both directions (Type II), small lesions at the IIIrd ventricle floor extending to the stalk (Type IV), and tumor localized in the stalk (Type V). S-GCTs almost uniformly presented as Type I-III, while most bifocal GCTs were Type IV with a larger pineal mass. These differences are significant as bifocal GCTs representing concurrent primaries or subependymal extension may be treated with whole ventricle radiation, while cerebrospinal fluid (CSF)-borne metastases warrant craniospinal irradiation (CSI). Although further study is necessary, we recommend CSI for bifocal GCTs exhibiting high-risk features such as metastasis or non-germinomatous germ cell tumor histology.

Indexed as

bifocal germ cell tumordual germ cell tumorgerminomaintracranial germ cell tumormagnetic resonance imagingnon-germinoma germ cell tumoroverall survivalprogression free survivalradiationsuprasellar tumor

Identifiers

PMID32937871
PMCPMC7565935
OpenAlexW3084820172

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.