Evidence map›Paper›PMID 35123517›Full record

ArticleRadiation oncology (London, England)2022

Clinical evaluation of two AI models for automated breast cancer plan generation.

Esther Kneepkens, Nienke Bakx, Maurice van der Sangen, Jacqueline Theuws, Peter-Paul van der Toorn, Dorien Rijkaart, Jorien van der Leer, Thérèse van Nunen, Els Hagelaar, Hanneke Bluemink and 1 more

Abstract read
In one paragraph

Article in Radiation oncology (London, England), 2022. 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
–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.

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.

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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

11 authors.

Esther Kneepkens *Department of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Nienke Bakx *Department of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Maurice van der SangenDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Jacqueline TheuwsDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Peter-Paul van der ToornDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Dorien RijkaartDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Jorien van der LeerDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Thérèse van NunenDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Els HagelaarDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Hanneke BlueminkDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.
Coen HurkmansDepartment of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands. coen.hurkmans@catharinaziekenhuis.nl.ORCID http://orcid.org/0000-0003-2268-0492

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArtificial intelligence (AI) shows great potential to streamline the treatment planning process. However, its clinical adoption is slow due to the limited number of clinical evaluation studies and because often, the translation of the predicted dose distribution to a deliverable plan is lacking. This study evaluates two different, deliverable AI plans in terms of their clinical acceptability based on quantitative parameters and qualitative evaluation by four radiation oncologists.

methodsFor 20 left-sided node-negative breast cancer patients, treated with a prescribed dose of 40.05 Gy, using tangential beam intensity modulated radiotherapy, two model-based treatment plans were evaluated against the corresponding manual plan. The two models used were an in-house developed U-net model and a vendor-developed contextual atlas regression forest model (cARF). Radiation oncologists evaluated the clinical acceptability of each blinded plan and ranked plans according to preference. Furthermore, a comparison with the manual plan was made based on dose volume histogram parameters, clinical evaluation criteria and preparation time.

resultsThe U-net model resulted in a higher average and maximum dose to the PTV (median difference 0.37 Gy and 0.47 Gy respectively) and a slightly higher mean heart dose (MHD) (0.01 Gy). The cARF model led to higher average and maximum doses to the PTV (0.30 and 0.39 Gy respectively) and a slightly higher MHD (0.02 Gy) and mean lung dose (MLD, 0.04 Gy). The maximum MHD/MLD difference was ≤ 0.5 Gy for both AI plans. Regardless of these dose differences, 90-95% of the AI plans were considered clinically acceptable versus 90% of the manual plans. Preferences varied between the radiation oncologists. Plan preparation time was comparable between the U-net model and the manual plan (287 s vs 253 s) while the cARF model took longer (471 s). When only considering user interaction, plan generation time was 121 s for the cARF model and 137 s for the U-net model.

conclusionsTwo AI models were used to generate deliverable plans for breast cancer patients, in a time-efficient manner, requiring minimal user interaction. Although the AI plans resulted in slightly higher doses overall, radiation oncologists considered 90-95% of the AI plans clinically acceptable.

Indexed as

Artificial IntelligenceRadiotherapy Planning, Computer-AssistedFemaleHumansUnilateral Breast NeoplasmsAutoplanningBreast cancercARFDeep learningDose mimickingU-net

Identifiers

PMID35123517
PMCPMC8817521

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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.