Evidence map›Paper›PMID 37102792›Full record

ArticleThe British journal of radiology2023

Isotoxic dose escalated radiotherapy for glioblastoma based on diffusion-weighted MRI and tumor control probability-an in-silico study.

Yaru Pang, Michael Kosmin, Zhuangling Li, Xiaonian Deng, Zihuang Li, Xianming Li, Ying Zhang, Gary Royle, Spyros Manolopoulos

Open access · greenAbstract read
In one paragraph

Article in The British journal of radiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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

9 authors at 3 institutions in 2 countries.

Yaru PangDepartment of Medical Physics and Biomedical Engineering, University College London, Gower Street, London, United Kingdom.
Michael KosminNeuro-Oncology Team, Department of Oncology, University College London Hospital NHS Foundation Trust, 250 Euston Road, London, United Kingdom.
Zhuangling LiDepartment of Radiation Oncology, Shenzhen People's Hospital, Shenzhen, China.
Xiaonian DengDepartment of Radiation Oncology, Shenzhen People's Hospital, Shenzhen, China.
Zihuang LiDepartment of Radiation Oncology, Shenzhen People's Hospital, Shenzhen, China.
Xianming LiDepartment of Radiation Oncology, Shenzhen People's Hospital, Shenzhen, China.
Ying ZhangDepartment of Medical Physics and Biomedical Engineering, University College London, Gower Street, London, United Kingdom.
Gary RoyleDepartment of Medical Physics and Biomedical Engineering, University College London, Gower Street, London, United Kingdom.
Spyros ManolopoulosDepartment of Medical Physics and Biomedical Engineering, University College London, Gower Street, London, United Kingdom.
ShenZhen People’s Hospital · CNUniversity College London · GBNational Institute for Health Research · GB

Funding

Cancer Research UK 28990
6 · The paper itself

Abstract

objectivesGlioblastoma (GBM) is the most common malignant primary brain tumor with local recurrence after radiotherapy (RT), the most common mode of failure. Standard RT practice applies the prescription dose uniformly across tumor volume disregarding radiological tumor heterogeneity. We present a novel strategy using diffusion-weighted (DW-) MRI to calculate the cellular density within the gross tumor volume (GTV) in order to facilitate dose escalation to a biological target volume (BTV) to improve tumor control probability (TCP).

methodsThe pre-treatment apparent diffusion coefficient (ADC) maps derived from DW-MRI of ten GBM patients treated with radical chemoradiotherapy were used to calculate the local cellular density based on published data. Then, a TCP model was used to calculate TCP maps from the derived cell density values. The dose was escalated using a simultaneous integrated boost (SIB) to the BTV, defined as the voxels for which the expected pre-boost TCP was in the lowest quartile of the TCP range for each patient. The SIB dose was chosen so that the TCP in the BTV increased to match the average TCP of the whole tumor.

resultsBy applying a SIB of between 3.60 Gy and 16.80 Gy isotoxically to the BTV, the cohort's calculated TCP increased by a mean of 8.44% (ranging from 7.19 to 16.84%). The radiation dose to organ at risk is still under their tolerance.

conclusionsOur findings indicate that TCPs of GBM patients could be increased by escalating radiation doses to intratumoral locations guided by the patient's biology ( ADVANCES IN KNOWLEDGE: A personalized and voxel level SIB radiotherapy method for GBM is proposed using DW-MRI, which can increase the tumor control probability and maintain organ at risk dose constraints.

Indexed as

GlioblastomaDiffusion Magnetic Resonance ImagingHumansMagnetic Resonance ImagingProbabilityRadiotherapy DosageRadiotherapy Planning, Computer-Assisted

Identifiers

PMID37102792
PMCPMC10230387
OpenAlexW4367174784

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.