Evidence map›Paper›PMID 23433793›Full record

ArticleInternational journal of radiation oncology, biology, physics2013

Management of pediatric spinal cord astrocytomas: outcomes with adjuvant radiation.

Zachary D Guss, Shalini Moningi, George I Jallo, Kenneth J Cohen, Moody D Wharam, Stephanie A Terezakis

Registry-linked trialAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04211974 (Genomic Landscape of Intramedullary Astrocytoma), which is not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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.

NCT04211974 unknown statusnot on this mapstarted 2019, after this paper: background citation

Genomic Landscape of Intramedullary Astrocytoma

TypeobservationalSponsorXuanwu Hospital, BeijingRan2019 to 2023Enrolled50ConditionsSpinal Cord AstrocytomaArmswhole-exome sequencing
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 40 citations in OpenAlex.

  1. Intramedullary pediatric low-grade glioma of the spine.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
  2. Astrocytomas of the spinal cord.Neuro-oncology advances · 2024
    Review
  3. Review
  4. Article
  5. Malignant Spinal Tumors.Advances in experimental medicine and biology · 2023
    Article
  6. Article
  7. Paediatric spinal cord low-grade gliomas-evaluation and management of post-surgical residual disease.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Article
  8. Review
  9. Article
  10. Pediatric primary high-grade spinal glioma: a National Cancer Database analysis of current patterns in treatment and outcomes.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  11. Article
  12. Article
  13. Pediatric intramedullary spinal cord tumor outcomes using the WeeFIM scale.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2018
    Article
  14. Review
  15. Article
  16. 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

6 authors at 2 institutions in 1 country.

Zachary D GussDepartment of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins Hospital, Baltimore, Maryland, USA.
Shalini Moningi
George I Jallo
Kenneth J Cohen
Moody D Wharam
Stephanie A Terezakis
Johns Hopkins Hospital · USJohns Hopkins University · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

purposePediatric intramedullary spinal cord tumors are exceedingly rare; in the United States, 100 to 200 cases are recognized annually, of these, most are astrocytomas. The purpose of this study is to report the outcomes in pediatric patients with spinal cord astrocytomas treated at a tertiary care center. METHODS AND MATERIALS: An institutional review board-approved retrospective single-institution study was performed for pediatric patients with spinal cord astrocytomas treated at our hospital from 1990 to 2010. The patients were evaluated on the extent of resection, progression-free survival (PFS), and development of radiation-related toxicities. Kaplan-Meier curves and multivariate regression model methods were used for analysis.

resultsTwenty-nine patients were included in the study, 24 with grade 1 or 2 (low-grade) tumors and 5 with grade 3 or 4 (high-grade) tumors. The median follow-up time was 55 months (range, 1-215 months) for patients with low-grade tumors and 17 months (range, 10-52 months) for those with high-grade tumors. Thirteen patients in the cohort received chemotherapy. All patients underwent at least 1 surgical resection. Twelve patients received radiation therapy to a median radiation dose of 47.5 Gy (range, 28.6-54.0 Gy). Fifteen patients with low-grade tumors and 1 patient with a high-grade tumor exhibited stable disease at the last follow-up visit. Acute toxicities of radiation therapy were low grade, whereas long-term sequelae were infrequent and manageable when they arose. All patients with low-grade tumors were alive at the last follow-up visit, compared with 1 patient with a high-grade tumor.

conclusionPrimary pediatric spinal cord astrocytomas vary widely in presentation and clinical course. Histopathologic grade remains a major prognostic factor. Patients with low-grade tumors tend to have excellent disease control and long-term survival compared to those with high-grade tumors. This experience suggests that radiation therapy may enhance tumor control with an acceptably low risk of long-term sequelae in this sensitive patient population.

Indexed as

AdolescentAstrocytomaBaltimoreChildChild, PreschoolDisease-Free SurvivalFemaleHumansMaleRadiation InjuriesRadiotherapy DosageRegression AnalysisRetrospective StudiesSpinal Cord NeoplasmsTertiary Care CentersTreatment Outcome

Identifiers

PMID23433793
PMCPMC4696045
OpenAlexW2045309587

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.