Evidence map›Paper›PMID 35275197›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2022

Temozolomide and Radiotherapy versus Radiotherapy Alone in Patients with Glioblastoma, IDH-wildtype: Post Hoc Analysis of the EORTC Randomized Phase III CATNON Trial.

C Mircea S Tesileanu, Marc Sanson, Wolfgang Wick, Alba A Brandes, Paul M Clement, Sara C Erridge, Michael A Vogelbaum, Anna K Nowak, Jean-Francois Baurain, Warren P Mason and 27 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00626990 (Phase III Trial on Concurrent and Adjuvant Temozolomide Chemotherapy in Non-1p/19q Deleted Anaplastic Glioma. The CATNON Intergroup Trial.), which is not on this map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 1% 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.

NCT00626990 phase3active not recruitingnot on this map

Phase III Trial on Concurrent and Adjuvant Temozolomide Chemotherapy in Non-1p/19q Deleted Anaplastic Glioma. The CATNON Intergroup Trial.

TypeinterventionalSponsorEuropean Organisation for Research and Treatment of Cancer - EORTCRan2007 to 2029Enrolled751ConditionsBrain and Central Nervous System TumorsArmstemozolomide, DNA methylation analysis, laboratory biomarker analysis, adjuvant therapy, quality-of-life assessment
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

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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

37 authors at 20 institutions in 10 countries.

C Mircea S TesileanuNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0003-3541-9242
Marc SansonSorbonne Université, Inserm, CNRS, UMR S 1127, Paris Brain Institute - Institut du Cerveau (ICM), AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière - Charles Foix, Service de Neurologie 2-Mazarin, Paris, France.ORCID 0000-0002-1813-8476
Wolfgang WickNeurology Department, University of Heidelberg, and Clinical Cooperation Unit Neurooncology, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-6171-634X
Alba A BrandesMedical Oncology Department, AUSL-IRCCS Scienze Neurologiche, Bologna, Italy.
Paul M ClementOncology Department, KU Leuven and General Medical Oncology Department, UZ Leuven, Leuven Cancer Institute, Leuven, Belgium.ORCID 0000-0001-7600-0806
Sara C ErridgeEdinburgh Centre for Neuro-Oncology, Western General Hospital, University of Edinburgh, Edinburgh, United Kingdom.
Michael A VogelbaumNeuro-Oncology Department, Moffitt Cancer Center, Tampa, Florida.
Anna K NowakMedical School, University of Western Australia, Crawley, Western Australia.ORCID 0000-0002-9317-9526
Jean-Francois BaurainMedical Oncology Department, King Albert II Cancer Institute, Cliniques universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.ORCID 0000-0003-4876-4600
Warren P MasonPrincess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
Helen WheelerNorthern Sydney Cancer Centre, University of Sydney, St Leonards, New South Wales, Australia.ORCID 0000-0002-6949-354X
Olivier L ChinotAix-Marseille University, AP-HM, Neuro-Oncology division, Marseille, France.ORCID 0000-0001-6317-9691
Sanjeev GillMedical Oncology Department, Alfred Hospital, Melbourne, Australia.
Matthew GriffinClinical Oncology Department, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Leland RogersRadiation Oncology Department, Gammawest Cancer Services, Salt Lake City, Utah.
Walter TaalNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0002-5530-7259
Roberta RudàNeuro-Oncology Department, City of Health and Science Hospital and University of Turin, Turin, Italy.
Michael WellerNeurology Department, Clinical Neuroscience Center, University Hospital and University of Zurich, Zurich, Switzerland.ORCID 0000-0002-1748-174X
Catherine McBainClinical Oncology Department, The Christie NHS FT, Manchester, United Kingdom.
Myra E van LindeMedical Oncology Department, Brain Tumor Center Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
Kenneth AldapePrincess Margaret Cancer Centre, University of Toronto, Toronto, Canada.ORCID 0000-0001-5119-7550
Robert B JenkinsDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Johan M KrosPathology Department, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0002-4727-0724
Pieter WesselingPathology Department, Amsterdam University Medical Centers, Amsterdam, the Netherlands.ORCID 0000-0001-5453-5201
Andreas von DeimlingNeuropathology Department, Ruprecht-Karls-University, and CCU Neuropathology German Cancer Institute and Consortium, DKFZ, and DKTK, Heidelberg, Germany.ORCID 0000-0002-5863-540X
Youri HoogstrateNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0003-2166-0676
Iris de HeerNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Peggy N AtmodimedjoPathology Department, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Hendrikus J DubbinkPathology Department, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0002-2160-5207
Rutger W W BrouwerCenter for Biomics, Erasmus MC, Rotterdam, the Netherlands.
Wilfred F J van IJckenCenter for Biomics, Erasmus MC, Rotterdam, the Netherlands.ORCID 0000-0002-0421-8301
Kin Jip CheungEORTC HQ, Brussels, Belgium.
Vassilis GolfinopoulosEORTC HQ, Brussels, Belgium.ORCID 0000-0002-8667-9477
Brigitta G BaumertRadiation-Oncology Department (MAASTRO), Maastricht University Medical Center (MUMC) and GROW (School for Oncology), Maastricht, the Netherlands.
Thierry GorliaEORTC HQ, Brussels, Belgium.
Pim J FrenchNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0002-0668-9529
Martin J van den BentNeurology Department, Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0001-5710-5127
Erasmus MC Cancer Institute · NLIneos (Belgium) · BEErasmus University Rotterdam · NLGerman Cancer Research Center · DEPrincess Margaret Cancer Centre · CAAmsterdam Neuroscience · NLAssistance Publique Hôpitaux de Marseille · FRCancer Institute of New South Wales · AUCancer Services · USCentre National de la Recherche Scientifique · FRCliniques Universitaires Saint-Luc · BECTO Hospital · ITIstituto delle Scienze Neurologiche di Bologna · ITKantonsspital Graubünden · CHMayo Clinic · USMoffitt Cancer Center · USNottingham University Hospitals NHS Trust · GBPrincess Máxima Center · NLRega Institute for Medical Research · BEThe Alfred Hospital · AU

Funding

NRG Oncology Network Group Operations Center - GY9 BIQSFP Reports/BudgetsU10CA180868 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI NORMAN WOLMARK · 2014 to 2026
$206.8M
Statistics CoreU10CA180822 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Elaina Harper · 2014 to 2026
$146.4M
Genomic Biomarkers of CancerZIABC011850 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ALDAPE, KENNETH · 2019 to 2025
$5.1M
UNDERSTANDING THE INTERACTIONS BETWEEN GERMLINE AND SOMATIC ALTERATIONS in the PATHOGENESIS OF GLIOMASR01CA230712 · NCI · MAYO CLINIC ROCHESTER · PI JENKINS, ROBERT B. · 2018 to 2022
$3.3M
Cancer Research UK CRUK/07/028NCI NIH HHS R01 CA230712NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868
6 · The paper itself

Abstract

purposeIn a post hoc analysis of the CATNON trial (NCT00626990), we explored whether adding temozolomide to radiotherapy improves outcome in patients with IDH1/2 wildtype (wt) anaplastic astrocytomas with molecular features of glioblastoma [redesignated as glioblastoma, isocitrate dehydrogenase-wildtype (IDH-wt) in the 2021 World Health Organization (WHO) classification of central nervous system tumors]. PATIENTS AND

methodsFrom the randomized phase III CATNON study examining the addition of adjuvant and concurrent temozolomide to radiotherapy in anaplastic astrocytomas, we selected a subgroup of IDH1/2wt and H3F3Awt tumors with presence of TERT promoter mutations and/or EGFR amplifications and/or combined gain of chromosome 7 and loss of chromosome 10. Molecular abnormalities including MGMT promoter methylation status were determined by next-generation sequencing, DNA methylation profiling, and SNaPshot analysis.

resultsOf the 751 patients entered in the CATNON study, 670 had fully molecularly characterized tumors. A total of 159 of these tumors met the WHO 2021 molecular criteria for glioblastoma, IDH-wt. Of these patients, 47 received radiotherapy only and 112 received a combination of radiotherapy and temozolomide. There was no added effect of temozolomide on either overall survival [HR, 1.19; 95% confidence interval (CI), 0.82-1.71] or progression-free survival (HR, 0.87; 95% CI, 0.61-1.24). MGMT promoter methylation was prognostic for overall survival, but was not predictive for outcome to temozolomide treatment either with respect to overall survival or progression-free survival.

conclusionsIn this cohort of patients with glioblastoma, IDH-wt temozolomide treatment did not add benefit beyond that observed from radiotherapy, regardless of MGMT promoter status. These findings require a new well-powered prospective clinical study to explore the efficacy of temozolomide treatment in this patient population.

Indexed as

AstrocytomaBrain NeoplasmsGlioblastomaAntineoplastic Agents, AlkylatingDacarbazineDNA MethylationDNA Modification MethylasesDNA Repair EnzymesHumansIsocitrate DehydrogenaseProspective StudiesTemozolomideAntineoplastic Agents, AlkylatingDacarbazineDNA Modification MethylasesDNA Repair EnzymesIsocitrate DehydrogenaseTemozolomide

Identifiers

PMID35275197
PMCPMC9297529
OpenAlexW4220938340

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Registered trials

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.