Evidence map›Paper›PMID 32564147›Full record

ArticleEuropean journal of pediatrics2021

Real-world data for pediatric medulloblastoma: can we improve outcomes?

Paula Sedano, Carmen González-San Segundo, Lourdes De Ingunza, Pedro Cuesta-Álvaro, Marta Pérez-Somarriba, Francisco Diaz-Gutiérrez, Carmen Garrido Colino, Alvaro Lassaletta

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Article in European journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Prognostic value of microRNA-125a expression status in molecular groups of pediatric medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Article
  5. Review
  6. Primary leptomeningeal medulloblastoma: a case-based review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022
    Review
  7. Article
  8. High expression of Toll-like receptor 7 is a survival factor in pediatric medulloblastoma.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Article
  9. Article
  10. 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.

Paula SedanoRadiation Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Carmen González-San SegundoRadiation Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Lourdes De IngunzaRadiation Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Pedro Cuesta-ÁlvaroComputing Services, Research Support, Complutense University of Madrid, Madrid, Spain.
Marta Pérez-SomarribaDepartment of Pediatric Oncology, Hospital Infantil Universitario Niño Jesús, Avenida Menéndez Pelayo, 65, 28009, Madrid, Spain.
Francisco Diaz-GutiérrezRadiation Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Carmen Garrido ColinoPediatric Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Alvaro LassalettaDepartment of Pediatric Oncology, Hospital Infantil Universitario Niño Jesús, Avenida Menéndez Pelayo, 65, 28009, Madrid, Spain. lassaalvaro@yahoo.com.ORCID http://orcid.org/0000-0003-2881-1473

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastoma (MB) is a malignant embryonal tumor that develops especially in childhood, with overall survival (OS) at 5 years of up to 70%. The objective of this study is to analyze treatment delivery variables in a retrospective cohort and evaluate the impact of these treatment quality parameters on survival. From 2000 to 2018, 40 pediatric patients with medulloblastoma, treated according to current international protocols, were retrospectively analyzed. Treatment delivery quality indicators were analyzed including the extent of surgery, radiotherapy (RT) parameters, and chemotherapy variables, related with time and dose-intensity deviations. With a median follow-up of 74 months (range, 6-195), OS at 5 years was 74 ± 7%, 81 ± 8% for standard-risk, and 55 ± 16% for high-risk patients (p = 0.090). Disease-free survival at 5 years was not significantly affected by extent of surgery (p = 0.428) and RT-related variables such as surgery-RT interval (p = 0.776) neither RT duration (p = 0.172) or maintenance chemotherapy compliance (p = 0.634). Multivariate analysis identified risk groups predictive of worse DFS (p = 0.032) and leptomeningeal dissemination associated with inferior OS (p = 0.029).Conclusion: Treatment delivery optimization has improved survival rates of patients with MB. Despite this, in our study, we have not established a clear influence of the considered radiotherapy and chemotherapy treatment quality parameters on outcomes. What is Known: • Improvement in treatment modalities during the last decades has reached a 5-year OS of up to 70% in these patients. • Extent of resection and radiotherapy parameters such as interval between surgery-radiotherapy and radiotherapy duration has been described as probable survival prognostic factors. What is New: • Differences in medulloblastoma survival rates between prospective studies and retrospective series. • The impact on survival of the three main treatment variables, surgery, radiotherapy and chemotherapy, susceptible to improvement.

Indexed as

Cerebellar NeoplasmsMedulloblastomaAntineoplastic Combined Chemotherapy ProtocolsChildHumansPrognosisProspective StudiesRetrospective StudiesSurvival RateTreatment OutcomeChildrenMedulloblastomaRadiotherapySurgerySurvivalTreatment quality

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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.