Evidence map›Paper›PMID 34550414›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Effects of different molecular subtypes and tumor biology on the prognosis of medulloblastoma.

Yavuz Aras, Duygu Dölen, Ayca İribas Çelik, Gozde Kılıç, Rejin Kebudi, Gökçen Ünverengil, Pulat Akın Sabancı, Ali Nail İzgi

Abstract read
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. 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

8 authors.

Yavuz ArasIstanbul Faculty of Medicine, Neurosurgery Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0001-8418-2291
Duygu DölenIstanbul Faculty of Medicine, Neurosurgery Department, Istanbul University, Istanbul, Turkey. dolenduygu@gmail.com.ORCID 0000-0002-6929-4401
Ayca İribas ÇelikIstanbul Faculty of Medicine, Radiation Oncology Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0002-1686-7114
Gozde KılıçIstanbul Faculty of Medicine, Pathology Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0001-8847-8831
Rejin KebudiInstitute of Oncology, Pediatric Hematology-Oncology Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-4344-8174
Gökçen ÜnverengilIstanbul Faculty of Medicine, Pathology Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-3177-7851
Pulat Akın SabancıIstanbul Faculty of Medicine, Neurosurgery Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0002-0283-0927
Ali Nail İzgiIstanbul Faculty of Medicine, Neurosurgery Department, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-0329-5089

Funding

Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi 34871
6 · The paper itself

Abstract

purposeMedulloblastoma is one of the most common malignant brain tumors in the pediatric population. Recent studies identified four distinct medulloblastoma subgroups with different molecular alterations and pathways, and natural courses and outcomes. To evaluate the results of surgical and medical treatments of patients with medulloblastoma and compare them among the medulloblastoma subgroups.

methodsThe clinical and radiological features, medical and surgical management and treatment outcomes and their correlation with molecular subgroups of 58 patients treated for medulloblastoma in the last 20 years were evaluated.

resultsFifty-eight patients, of whom 35 were male and 23 were female, were evaluated. The median age was 6 years (range, 1-19 years). The most common symptoms were nausea and vomiting (60%). Forty-three percent of the patients had headache and 40% had ataxia. Previous pathology reports revealed that 43 (74%), eight (14%), five (8%), and two (3%) had classic, desmoplastic, desmoplastic/nodular, and anaplastic morphologies, respectively. After the subgroup analyses, five patients (12%) were attributed to the wingless subgroup (WNT) group; 14 (32.5%), to the sonic hedgehog subgroup (SHH) group; and 24 (56%), to the non-WNT non-SHH group. On the basis of immunohistochemical analysis results, 15 patients could not be attributed to any subgroups. The clinical risk groups (average vs high-risk) and age at diagnosis (≥ 3 years vs < 3 years of age) were significant for 5-year event free survival (86% vs 43%, p:0.011 and 59% vs 36%, p:0.039). There was no significant difference in survival or event free survival according to molecular subtypes in this cohort.

conclusionIn corporation of molecular features to the clinicopathologic classification leads to risk-adapted treatment. Although the molecular subgroups did not affect outcome significantly in this study, more studies with larger numbers of patients are needed to understand the tumor pathophysiology of medulloblastoma and design the future medical practice.

Indexed as

Cerebellar NeoplasmsMedulloblastomaAdolescentChildChild, PreschoolFemaleHumansInfantMalePrognosisYoung AdultImmunohistochemistryMalignant childhood brain tumorMedulloblastomaNeurooncologyTumor biology

Identifiers

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.