Evidence map›Paper›PMID 38765202›Full record

ArticleClinical and translational radiation oncology2024

Dummy run for planning of isotoxic dose-escalated radiation therapy for glioblastoma used in the PRIDE trial (NOA-28; ARO-2024-01; AG-NRO-06).

Sebastian H Maier, Stephan Schönecker, Vasiliki Anagnostatou, Sylvia Garny, Alexander Nitschmann, Daniel F Fleischmann, Marcel Büttner, David Kaul, Detlef Imhoff, Emmanouil Fokas and 19 more

Registry-linked trialAbstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05871021 (A Phase IIa, Open-label, Multicenter Study of Radiochemotherapy With Isotoxic Dose Escalation and Protective VEGF Inhibition Using Bevacizumab in the Treatment of Patients With First Diagnosis of IDH Wild-type, MGMT Unmethylated Glioblastoma), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

NCT05871021 phase2recruitingnot on this map

A Phase IIa, Open-label, Multicenter Study of Radiochemotherapy With Isotoxic Dose Escalation and Protective VEGF Inhibition Using Bevacizumab in the Treatment of Patients With First Diagnosis of IDH Wild-type, MGMT Unmethylated Glioblastoma

TypeinterventionalSponsorUniversity Hospital TuebingenRan2024 to 2028Enrolled146ConditionsGlioblastomaArmsDose escalation of radiation dose beyond the therapeutic standard
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Isotoxic stereotactic reirradiation for recurrent pelvic cancers.Physics and imaging in radiation oncology · 2026
    Article
  5. 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

29 authors.

Sebastian H MaierDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Stephan SchöneckerDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Vasiliki AnagnostatouDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Sylvia GarnyDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Alexander NitschmannDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Daniel F FleischmannDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Marcel BüttnerDepartment of Radiation Oncology, University Hospital Tübingen, Tübingen, Germany.
David KaulDepartment of Radiation Oncology and Radiotherapy, Charité-Universitätsmedizin Berlin (Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health), Berlin, Germany.
Detlef ImhoffDepartment of Radiotherapy of Oncology, University of Frankfurt, Frankfurt, Germany.
Emmanouil FokasDepartment of Radiotherapy of Oncology, University of Frankfurt, Frankfurt, Germany.
Clemens SeidelDepartment of Radiation Oncology, University Hospital Leipzig, University of Leipzig, Leipzig, Germany.
Peter HauDepartment of Neurology and Wilhelm Sander-NeuroOncology Unit, Regensburg University Hospital, Regensburg, Germany.
Oliver KölblDepartment of Radiotherapy, University Medical Center Regensburg, Regensburg, Germany.
Ilinca PoppDepartment of Radiation Oncology, University of Freiburg Faculty of Medicine, Freiburg, Germany.
Anca-Ligia GrosuDepartment of Radiation Oncology, University of Freiburg Faculty of Medicine, Freiburg, Germany.
Jan HaussmannDepartment of Radiation Oncology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University, Düsseldorf, Germany.
Wilfried BudachDepartment of Radiation Oncology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University, Düsseldorf, Germany.
Eren CelikDepartment of Radiation Oncology, CyberKnife and Radiation Therapy, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany.
Klaus-Henning KahlDepartment of Radiooncology, University Hospital Augsburg, Augsburg, Germany.
Elgin HoffmannDepartment of Radiation Oncology, University Hospital Tübingen, Tübingen, Germany.
Ghazaleh TabatabaiDepartment of Neurology and Interdisciplinary Neuro-Oncology, University Hospital Tübingen, Hertie Institute for Clinical Brain Research, Tübingen, Germany.
Frank PaulsenDepartment of Radiation Oncology, University Hospital Tübingen, Tübingen, Germany.
Adrien HolzgreveDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.
Nathalie L AlbertDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.
Ulrich MansmannInstitute for Medical Information Processing, Biometry and Epidemiology, Faculty of Medicine, LMU Munich, Munich, Germany.
Stefanie CorradiniDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Claus BelkaDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Maximilian NiyaziDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Raphael BodensohnDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The PRIDE trial (NOA-28; ARO-2024-01; AG-NRO-06; NCT05871021) is designed to determine whether a dose escalation with 75.0 Gy in 30 fractions can enhance the median overall survival (OS) in patients with methylguanine methyltransferase (MGMT) promotor unmethylated glioblastoma compared to historical median OS rates, while being isotoxic to historical cohorts through the addition of concurrent bevacizumab (BEV). To ensure protocol-compliant irradiation planning with all study centers, a dummy run was planned and the plan quality was evaluated. Methods: A suitable patient case was selected and the computed tomography (CT), magnetic resonance imaging (MRI) and O-(2-[ Results: Median DSC was 0.89, 0.90, 0.88 for PTV60, PTV60ex (planning target volume receiving 60.0 Gy for the standard and the experimental plan, respectively) and PTV75 (PTV receiving 75.0 Gy in the experimental plan), respectively. Median HD values were 17.0 mm, 13.9 mm and 12.1 mm, respectively. These differences were also evident in the volumes: The PTV60 had a volume range of 219.1-391.3 cc (median: 261.9 cc) for the standard plans, while the PTV75 volumes for the experimental plans ranged from 71.5-142.7 cc (median: 92.3 cc). The structures with the largest deviations in Dice score were the pituitary gland (median 0.37, range 0.00-0.69) and the right lacrimal gland (median 0.59, range 0.42-0.78). Conclusions: The deviations revealed the necessity of systematic trainings with appropriate feedback before the start of clinical trials in radiation oncology and the constant monitoring of protocol compliance throw-out the study. Trial registration: NCT05871021.

Indexed as

BevacizumabDose EscalationFET PETGlioblastomaPRIDE TrialQA

Identifiers

PMID38765202
PMCPMC11101689

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Registered trials

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