Evidence map›Paper›PMID 33458271›Full record

ArticlePhysics and imaging in radiation oncology2019

Planning feasibility of extremely hypofractionated prostate radiotherapy on a 1.5 T magnetic resonance imaging guided linear accelerator.

Mariska D den Hartogh, Hans C J de Boer, Eline N de Groot-van Breugel, Jochem R N van der Voort van Zyp, Jochem Hes, Uulke A van der Heide, Floris Pos, Karin Haustermans, Tom Depuydt, Robert Jan Smeenk and 3 more

Open access · goldAbstract read
In one paragraph

Article in Physics and imaging in radiation oncology, 2019. 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
3.6field-weighted citation impact, top 7% 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, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Imaging science and development in modern high-precision radiotherapy.Physics and imaging in radiation oncology · 2019
    Article
  8. Article
  9. 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

13 authors at 5 institutions in 2 countries.

Mariska D den HartoghDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Hans C J de BoerDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Eline N de Groot-van BreugelDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Jochem R N van der Voort van ZypDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Jochem HesDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Uulke A van der HeideDepartment of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Floris PosDepartment of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Karin HaustermansDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Tom DepuydtDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Robert Jan SmeenkDepartment of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Martina Kunze-BuschDepartment of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Bas W RaaymakersDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Linda G W KerkmeijerDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
University Medical Center Utrecht · NLKU Leuven · BERadboud University Nijmegen · NLThe Netherlands Cancer Institute · NLRadboud University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeRecently, intermediate and high-risk prostate cancer patients have been treated in a multicenter phase II trial with extremely hypofractionated prostate radiotherapy (hypo-FLAME trial). The purpose of the current study was to investigate whether a 1.5 T magnetic resonance imaging guided linear accelerator (MRI-linac) could achieve complex dose distributions of a quality similar to conventional linac state-of-the-art prostate treatments. MATERIALS AND

methodsThe clinically delivered treatment plans of 20 hypo-FLAME patients (volumetric modulated arc therapy, 10 MV, 5 mm leaf width) were included. Prescribed dose to the prostate was 5 × 7 Gy, with a focal tumor boost up to 5 × 10 Gy. MRI-linac treatment plans (intensity modulated radiotherapy, 7 MV, 7 mm leaf width, fixed collimator angle and 1.5 T magnetic field) were calculated. Dose distributions were compared.

resultsIn both conventional and MRI-linac treatment plans, the V35Gy to the whole prostate was >99% in all patients. Mean dose to the gross tumor volume was 45 Gy for conventional and 44 Gy for MRI-linac plans, respectively. Organ at risk doses were met in the majority of plans, except for a rectal V35Gy constraint, which was exceeded in one patient, by 1 cc, for both modalities. The bladder V32Gy and V28Gy constraints were exceeded in two and one patient respectively, for both modalities.

conclusionPlanning of stereotactic radiotherapy with focal ablative boosting in prostate cancer on a high field MRI-linac is feasible with the current MRI-linac properties, without deterioration of plan quality compared to conventional treatments.

Indexed as

Focal boostHypofractionationMRI-linacProstate cancerStereotactic body radiotherapy

Identifiers

PMID33458271
PMCPMC7807729
OpenAlexW2957527574

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.