Evidence map›Paper›PMID 38756654›Full record

ArticleFrontiers in oncology2024

Impact of treatment and clinical characteristics on the survival of children with medulloblastoma in Mexico.

Violeta Salceda-Rivera, Isidoro Tejocote-Romero, Diana S Osorio, Rosalba Bellido-Magaña, Araceli López-Facundo, Susana E Anaya-Aguirre, Daniel Ortiz-Morales, Roberto Rivera-Luna, Evelyne Reyes-Gutiérrez, Rebeca Rivera-Gómez and 18 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

28 authors.

Violeta Salceda-RiveraHospital Civil de Guadalajara "Dr. Juan I. Menchaca", Department of Pediatrics, Divisions of Pediatric Hematology-Oncology, Guadalajara, Jalisco, Mexico.
Isidoro Tejocote-RomeroIMIEM, Instituto Materno Infantil del Estado de Mexico, Secretaria de Salud, Toluca, Estado de Mexico, Mexico.
Diana S OsorioICON PLC, Clinical Research Organization, Dublin, Ireland.
Rosalba Bellido-MagañaHospital General Regional de Leon, Leon, Guanajuato, Mexico.
Araceli López-FacundoDepartment of Pediatric Oncology, ISSEMYM, Instituto de Seguridad Social del Estado de México y Municipios, Toluca, Estado de Mexico, Mexico.
Susana E Anaya-AguirreInstituto Mexicano del Seguro Social, Centro Médico Nacional La Raza, Mexico City, Mexico.
Daniel Ortiz-MoralesDepartment of Pediatric Oncology, Hospital General de México "Dr. Eduardo Liceaga", Mexico City, Mexico.
Roberto Rivera-LunaDepartment of Pediatric Oncology, Instituto Nacional de Pediatria, Mexico City, Mexico.
Evelyne Reyes-GutiérrezHospital de Especialidades del Niño y de la Mujer, Secretaria de Salud, Queretaro, Mexico.
Rebeca Rivera-GómezHospital General de Tijuana, Universidad Autonoma de Baja California, Tijuana, Baja California, Mexico.
Liliana Velasco-HidalgoDepartment of Pediatric Oncology, Instituto Nacional de Pediatria, Mexico City, Mexico.
Deyanira Cortés-AlvaHospital del Niño DIF Hidalgo, Sistema Nacional para el Desarrollo Integral de la Familia, Hidalgo, Mexico.
Sandra Lagarda-ArrecheaDepartment of Pediatric Oncology, Instituto Estatal de Cancerologia, Colima, Mexico.
Farina E Arreguín-GonzálezCentro Médico Nacional "20 de Noviembre" del Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Mexico City, Mexico.
Alma E Benito-ReséndizCentro Médico Nacional "20 de Noviembre" del Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Mexico City, Mexico.
Silvia Chávez-GallegosDepartment of Pediatric Oncology, Hospital Infantil "Eva Samano de López Mateos", Morelia, Michoacan, Mexico.
Eloy Pérez-RiveraDepartment of Pediatric Oncology, Hospital Infantil "Eva Samano de López Mateos", Morelia, Michoacan, Mexico.
Guillermo J Gaytán-FernándezHospital General Regional de Leon, Leon, Guanajuato, Mexico.
José A León-EspitiaHospital General Regional de Leon, Leon, Guanajuato, Mexico.
Jociela Domínguez-SánchezDepartment of Pediatric Oncology, Centenario Hospital Miguel Hidalgo, Aguascalientes, Mexico.
Carlos Leal-CavazosHospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo Leon, Nuevo Leon, Mexico.
Citlalli Simón-GonzálezDepartment of Pediatric Oncology, Hospital Regional de Alta Especialidad del Niño " Dr. Rodolfo Nieto Padrón", Tabasco, Mexico.
Tania C Larios-FarakDepartment of Pediatric Oncology, Hospital Infantil del Estado de Sonora, Hermosillo, Sonora, Mexico.
Nubia A Macías-GarcíaDepartment of Pediatric Oncology, Hospital del Niño "Dr. Federico Gómez Santos", Saltillo, Coahuila, Mexico.
Ana C García-EspinosaDepartment of Pediatric Oncology, Hospital Infantil de Especialidades de Chihuahua, Chihuahua, Chihuahua, Mexico.
Francisco Guerrero-MaymesDepartment of Pediatric Oncology, Hospital General de Occidente, Zapopan, Jalisco, Mexico.
Paola Casillas-ToralHospital Civil de Guadalajara "Dr. Juan I. Menchaca", Department of Pediatrics, Divisions of Pediatric Hematology-Oncology, Guadalajara, Jalisco, Mexico.
Oscar González-RamellaHospital Civil de Guadalajara "Dr. Juan I. Menchaca", Department of Pediatrics, Divisions of Pediatric Hematology-Oncology, Guadalajara, Jalisco, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Data on medulloblastoma outcomes and experiences in low- and middle-income countries, especially in Latin America, is limited. This study examines challenges in Mexico's healthcare system, focusing on assessing outcomes for children with medulloblastoma in a tertiary care setting. Methods: A retrospective analysis was conducted, involving 284 patients treated at 21 pediatric oncology centers in Mexico. Results: High-risk patients exhibited markedly lower event-free survival than standard-risk patients (43.5% vs. 78.3%, p<0.001). Influential factors on survival included anaplastic subtype (HR 2.4, p=0.003), metastatic disease (HR 1.9, p=0.001); residual tumor >1.5cm², and lower radiotherapy doses significantly impacted event-free survival (EFS) and overall survival (OS). Platinum-based chemotherapy showed better results compared to the ICE protocol in terms of OS and EFS, which was associated with higher toxicity. Patients under 3 years old displayed notably lower OS and EFS compared to older children (36.1% vs. 55.9%, p=0.01).

Indexed as

brain tumorchildhoodclinical characteristicsCNS tumorslow and middle income countriesmedulloblastomasurvival

Identifiers

PMID38756654
PMCPMC11096484

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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.