ArticleAdvances in radiation oncology2024
Automatic Treatment Planning for Radiation Therapy: A Cross-Modality and Protocol Study.
Article in Advances in radiation oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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.
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Who cites it
2 citing papers in PubMed.
- A rule-based, feedback-driven framework for fully automated prostate VMAT planning.Journal of applied clinical medical physics · 2026Article
- Multicenter study on the versatility and adoption of AI-driven automated radiotherapy planning across cancer types.Nature communications · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Purpose: This study investigated the applicability of 3-dimensional dose predictions from a model trained on one modality to a cross-modality automated planning workflow. Additionally, we explore the impact of integrating a multicriteria optimizer (MCO) on adapting predictions to different clinical preferences. Methods and Materials: Using a previously created 3-stage U-Net in-house model trained on the 2020 American Association of Physicists in Medicine OpenKBP challenge data set (340 head and neck plans, all planned using 9-field static intensity modulated radiation therapy [IMRT]), we retrospectively generated dose predictions for 20 patients. These dose predictions were, in turn, used to generate deliverable IMRT, VMAT, and tomotherapy plans using the fallback plan functionality in Raystation. The deliverable plans were evaluated against the dose predictions based on primary clinical goals. A new set of plans was also generated using MCO-based optimization with predicted dose values as constraints. Delivery QA was performed on a subset of the plans to assure clinical deliverability. Results: The mimicking approach accurately replicated the predicted dose distributions across different modalities, with slight deviations in the spinal cord and external contour maximum doses. MCO optimization significantly reduced doses to organs at risk, which were prioritized by our institution while maintaining target coverage. All tested plans met clinical deliverability standards, evidenced by a gamma analysis passing rate >98%. Conclusions: Our findings show that a model trained only on IMRT plans can effectively contribute to planning across various modalities. Additionally, integrating predictions as constraints in an MCO-based workflow, rather than direct dose mimicking, enables a flexible, warm-start approach for treatment planning, although the benefit is reduced when the training set differs significantly from an institution's preference. Together, these approaches have the potential to significantly decrease plan turnaround time and quality variance, both at high-resource medical centers that can train in-house models and smaller centers that can adapt a model from another institution with minimal effort.
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Registered trials
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.