Evidence map›Paper›PMID 36354288›Full record

ArticleMedical physics2023

The dosimetric error due to uncorrected tumor rotation during real-time adaptive prostate stereotactic body radiation therapy.

Chandrima Sengupta, Simon Skouboe, Thomas Ravkilde, Per Rugaard Poulsen, Doan Trang Nguyen, Peter B Greer, Trevor Moodie, Nicholas Hardcastle, Amy J Hayden, Sandra Turner and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Medical physics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 15 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

16 authors at 7 institutions in 2 countries.

Chandrima SenguptaACRF Image X Institute, University of Sydney, Sydney, New South Wales, Australia.
Simon SkouboeDanish Center for Particle Therapy, Aarhus University Hospital, Aarhus, Denmark.
Thomas RavkildeDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Per Rugaard PoulsenDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Doan Trang NguyenACRF Image X Institute, University of Sydney, Sydney, New South Wales, Australia.
Peter B GreerDepartment of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.
Trevor MoodieCrown Princess Mary Cancer Center, Sydney, New South Wales, Australia.
Nicholas HardcastlePeter MacCallum Cancer Center, Melbourne, Victoria, Australia.
Amy J HaydenCrown Princess Mary Cancer Center, Sydney, New South Wales, Australia.
Sandra TurnerCrown Princess Mary Cancer Center, Sydney, New South Wales, Australia.
Shankar SivaPeter MacCallum Cancer Center, Melbourne, Victoria, Australia.
Keen-Hun TaiSir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.
Jarad MartinDepartment of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.
Jeremy T BoothNorthern Sydney Cancer Center, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Ricky O'BrienACRF Image X Institute, University of Sydney, Sydney, New South Wales, Australia.
Paul J KeallACRF Image X Institute, University of Sydney, Sydney, New South Wales, Australia.
University of Sydney · AUAarhus University Hospital · DKCancer Australia · AUCalvary Mater Newcastle Hospital · AUPeter MacCallum Cancer Centre · AURoyal North Shore Hospital · AUUniversity of Melbourne · AU

Funding

Cancer Australia APP1081534Cancer Australia APP1085360Prostate Cancer Foundation of Australia (PCFA)
6 · The paper itself

Abstract

backgroundDuring prostate stereotactic body radiation therapy (SBRT), prostate tumor translational motion may deteriorate the planned dose distribution. Most of the major advances in motion management to date have focused on correcting this one aspect of the tumor motion, translation. However, large prostate rotation up to 30° has been measured. As the technological innovation evolves toward delivering increasingly precise radiotherapy, it is important to quantify the clinical benefit of translational and rotational motion correction over translational motion correction alone. PURPOSE: The purpose of this work was to quantify the dosimetric impact of intrafractional dynamic rotation of the prostate measured with a six degrees-of-freedom tumor motion monitoring technology.

methodsThe delivered dose was reconstructed including (a) translational and rotational motion and (b) only translational motion of the tumor for 32 prostate cancer patients recruited on a 5-fraction prostate SBRT clinical trial. Patients on the trial received 7.25 Gy in a treatment fraction. A 5 mm clinical target volume (CTV) to planning target volume (PTV) margin was applied in all directions except the posterior direction where a 3 mm expansion was used. Prostate intrafractional translational motion was managed using a gating strategy, and any translation above the gating threshold was corrected by applying an equivalent couch shift. The residual translational motion is denoted as

resultsFractional data analysis shows that the dose differences from the plan (both ΔD(

conclusionsThe dosimetric impact of tumor rotation on a large prostate cancer patient cohort was quantified in this study. These results suggest that the standard 3-5 mm CTV-PTV margin was sufficient to account for the intrafraction prostate rotation observed for this cohort of patients, provided an appropriate gating threshold was applied to correct for translational motion. Residual dose errors due to uncorrected prostate rotation were small in magnitude, which may be corrected using different treatment adaptation strategies to further improve the dosimetric accuracy.

Indexed as

Prostatic NeoplasmsRadiosurgeryRadiotherapy, Intensity-ModulatedHumansMaleProstateRadiotherapy DosageRadiotherapy Planning, Computer-AssistedRotationmotion-induced dose errormotion managementtumor motion

Identifiers

PMID36354288
PMCPMC10099881
OpenAlexW4308680868

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Registered trials

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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.