Evidence map›Paper›PMID 38578306›Full record

ArticleNeuro-oncology2024

Treatment response as surrogate to predict risk for disease progression in pediatric medulloblastoma with persistent magnetic resonance imaging lesions after first-line treatment.

Denise Obrecht-Sturm, Lena Schömig, Martin Mynarek, Brigitte Bison, Rudolf Schwarz, Torsten Pietsch, Stefan M Pfister, Martin Sill, Dominik Sturm, Felix Sahm and 8 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

18 authors at 9 institutions in 3 countries.

Denise Obrecht-SturmPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-3216-8452
Lena SchömigPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin MynarekMildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-3302-2719
Brigitte BisonDepartment of Neuroradiology, University Hospital Augsburg, Augsburg, Germany.
Rudolf SchwarzDepartment for Radiotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Torsten PietschInstitute of Neuropathology, Brain Tumor Reference Center of the German Society for Neuropathology and Neuroanatomy (DGNN), University of Bonn, DZNE German Center for Neurodegenerative Diseases, Bonn, Germany.
Stefan M PfisterDepartment of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-5447-5322
Martin SillDepartment of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Dominik SturmPediatric Glioma Research Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Felix SahmCCU Neuropathology, German Cancer Research Center (DKFZ) and German Consortium for Translational Cancer Research (DKTK), Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-5441-1962
Rolf-Dieter KortmannDepartment of Radiation Oncology, University Hospital Leipzig, Leipzig, Germany.
Nicolas U GerberDepartment of Pediatric Oncology, University Children's Hospital Zürich, Zürich, Switzerland.
André O von BuerenDivision of Pediatric Hematology and Oncology, Department of Pediatrics, Obstetrics and Gynecology, University Hospital of Geneva, Geneva, Switzerland.
Gudrun FleischhackPediatrics III, Pediatric Oncology and Hematology, University Hospital Essen, Essen, Germany.
Ulrich SchüllerResearch Institute Kinderkrebs-Zentrum Hamburg, Hamburg, Germany.ORCID 0000-0002-8731-1121
Gunther NussbaumerDivision of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Martin BeneschDivision of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria.
Stefan RutkowskiPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Universität Hamburg · DEGerman Cancer Research Center · DEMedical University of Graz · ATEssen University Hospital · DEUniversity Children's Hospital Zurich · CHUniversity Hospital Augsburg · DEUniversity Hospital Leipzig · DEUniversity Hospital of Geneva · CHUniversity of Bonn · DE

Funding

Deutsche KinderkrebsstiftungGerman Children's Cancer FoundationSteirische Kinderkrebshilfe
6 · The paper itself

Abstract

backgroundThis study aims at clarifying the impact of persistent residual lesions following first-line treatment for pediatric medulloblastoma.

methodsData on 84 pediatric patients with medulloblastoma and persistent residual lesions on centrally reviewed magnetic resonance imaging (MRI) at the end of first-line therapy were analyzed.

resultsTwenty patients (23.8%) had residual lesions in the tumor bed (R+/M0), 51 (60.7%) had distant lesions (R0/M+) and 13 (15.5%) had both (R+/M+). Overall response to first-line therapy was minor or partial (≥ 25% reduction, minor response [MR]/PR) for 64 (76.2%) and stable disease (SD) for 20 patients (23.8%). Five-year post-primary-treatment progression-free (pptPFS) and overall survival (pptOS) were superior after MR/PR (pptPFS: 62.5 ± 7.0%[MR/PR] vs. 35.9 ± 12.8%[SD], P = .03; pptOS: 79.7 ± 5.9[MR/PR] vs. 55.5 ± 13.9[SD], P = .04). Furthermore, R+/M + was associated with a higher risk for progression (5-year pptPFS: 22.9 ± 17.9%[R+, M+] vs. 72.4 ± 12.0%[R+, M0]; P = .03). Watch-and-wait was pursued in 58 patients, while n = 26 received additional treatments (chemotherapy only, n = 19; surgery only, n = 2; combined, n = 3; valproic acid, n = 2), and their outcomes were not superior to watch-and-wait (5-year pptPFS: 58.5 ± 7.7% vs. 51.6 ± 10.7% P = .71; 5-year pptOS: 76.3 ± 6.9% vs. 69.8 ± 9.7%, P = .74). For the whole cohort, 5-year pptPFS by molecular subgroup (58 cases) were WNT: 100%, SHH: 50.0 ± 35.4%, group-4, 52.5 ± 10.5, group-3 54.2 ± 13.8%; (P = .08).

conclusionsOverall response and extent of lesions can function as surrogate parameters to predict outcomes in pediatric MB patients with persistent lesions after first-line therapy. Especially in the case of solitary persistent medulloblastoma MRI lesions, additional therapy was not beneficial. Therefore, treatment response, extent/kind of residual lesions and further diagnostic information need consideration for indication of additional treatments for persisting lesions.

Indexed as

Cerebellar NeoplasmsDisease ProgressionMagnetic Resonance ImagingMedulloblastomaAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleNeoplasm, ResidualPrognosisRetrospective StudiesSurvival RatechildrenmedulloblastomaMRIpersistent residual disease

Identifiers

PMID38578306
PMCPMC11376455
OpenAlexW4394019153

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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.