Evidence map›Paper›PMID 38465768›Full record

ArticleNeuro-oncology2024

Very long-term outcomes of pediatric patients treated for optic pathway gliomas: A longitudinal cohort study.

Alice Morin, Rodrigue Allodji, Dulanjalee Kariyawasam, Philippe Touraine, Stéphanie Puget, Kevin Beccaria, Emilie De Carli, Virginie Kieffer, Sophie Rivollet, Samuel Abbou and 7 more

Open access · greenAbstract read
In one paragraph

Article in Neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Surgical options of chiasmatic hypothalamic glioma-a relevant part of therapy in an interdisciplinary approach for tumor control.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Article
  8. Paediatric low-grade glioma: the role of classical pathology in integrated diagnostic practice.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024
    Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 1 country.

Alice MorinDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.ORCID 0009-0009-5259-0181
Rodrigue AllodjiRadiation Epidemiology Group, INSERM Unit 1018, Villejuif, France.
Dulanjalee KariyawasamDepartment of Pediatric Endocrinology, Diabetology and Gynaecology, Necker-Enfants Malades University Hospital, Paris cite University, Paris, France.ORCID 0000-0002-3870-202X
Philippe TouraineDepartment of Endocrinology and Reproductive Medicine, Pitie-Salpetriere Hospital, Sorbonne University, Paris, France.ORCID 0000-0002-8462-7753
Stéphanie PugetNeuro-surgery Department, Necker-Enfants Malades University Hospital, Paris cite University, Paris, France.
Kevin BeccariaNeuro-surgery Department, Necker-Enfants Malades University Hospital, Paris cite University, Paris, France.ORCID 0000-0002-3405-1944
Emilie De CarliDepartment of Children and Adolescents Onco-hematology, Angers University Hospital, Angers, France.
Virginie KiefferMonitoring and Integration Center for Children with Acquired Brain Damage, Saint-Maurice Hospital, Saint-Maurice, France.
Sophie RivolletDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.
Samuel AbbouDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.
Chiraz FayechDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.
Vincent SouchardRadiation Epidemiology Group, INSERM Unit 1018, Villejuif, France.
Christelle DufourDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.ORCID 0000-0001-5993-8077
Florent De VathaireRadiation Epidemiology Group, INSERM Unit 1018, Villejuif, France.ORCID 0000-0002-8374-9281
Stéphanie BolleRadiation Oncology Department, Gustave Roussy, Paris-Saclay University, Villejuif, France.
Jacques GrillDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.ORCID 0000-0003-4773-3001
Brice FresneauDepartment of Children and Adolescents Oncology, Gustave Roussy, Paris-Saclay University, Villejuif, France.ORCID 0000-0001-7603-7828
Université Paris-Saclay · FRInserm · FRHôpital Necker-Enfants Malades · FRHôpitaux de Saint Maurice · FRSorbonne Université · FRUniversité d'Angers · FR

Funding

French Society of Childhood and Adolescent CancerThe Fondation ARCThe Gustave Roussy Foundatio
6 · The paper itself

Abstract

backgroundOptic pathway gliomas (OPGs) represent 5% of childhood brain tumors. Successive relapses lead to multiple treatments exposing to late complications.

methodsWe included patients treated at Gustave Roussy (GR) between January 1980 and December 2015 for OPG, before 18 years old and alive at 5 years from diagnosis. Mortality and physical health conditions data were extracted from medical data files and updated, thanks to the GR long-term follow-up program and French national mortality registry for patients included in the French Childhood Cancer Survivor Study.

resultsWe included 182 5-year OPG-childhood survivors in the analysis (sex ratio M/F 0.8, 35% with neurofibromatosis type 1 [NF1]). With a median follow-up of 17.2 years (range = 5-41), we registered 82 relapses, 9 second malignancies, and 15 deaths as first events after 5 years, resulting in 20-year conditional overall survival (C-OS) and late events-free survival of 79.9% (95% confidence interval [CI] = 71-86) and 43.5% (95% CI = 36-51), respectively. Radiotherapy exposure in NF1 patients (hazard ratio [HR] = 6, 95% CI = 1.7-21.2) and hypothalamic involvement (HR = 3.2, 95% CI = 1.4-7.3) were significantly associated with C-OS in multivariable analyses. Ninety-five percent of 5-year OPG survivors suffered from any health condition, especially visual acuity "<1/10" (n = 109), pituitary deficiency (n = 106), and neurocognitive impairment (n = 89). NF1 (HR 2.1) was associated with precocious puberty. With a median time post-diagnosis of 4.2 years, 33 cerebrovascular events were observed in 21 patients.

conclusionsLate relapses, second malignancies, and cerebrovascular diseases are severe late events resulting in premature mortality. Morbidity is high and needs after-cancer care to improve quality of life. Risk factors could be considered to better stratify long-term follow-up.

Indexed as

Optic Nerve GliomaAdolescentAdultCancer SurvivorsChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantInfant, NewbornLongitudinal StudiesMaleNeoplasm Recurrence, LocalNeurofibromatosis 1Prognosislong-term outcomeoptic pathway gliomapediatric

Identifiers

PMID38465768
PMCPMC11226872
OpenAlexW4392637044

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.