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Updated: Jan 14, 2026

Dynamic Lung Tumor Tracking for Stereotactic Ablative Body Radiation Therapy
Published on: June 7, 2015
First experimental demonstration of magnetic resonance-guided multileaf collimator tracking for
Prescilla Uijtewaal1, Pim T S Borman1, Peter L Woodhead1,2
1Department of Radiotherapy, University Medical Center Utrecht, The Netherlands.
Background And Purpose:
(Ultra-)hypofractionated radiotherapy is an effective treatment for localized prostate cancer, but intrafraction motion can increase toxicity and/or reduce treatment efficacy. Therefore, motion management is essential. This study explores magnetic resonance imaging (MRI)-guided multileaf collimator (MLC) tracking for 2-fraction prostate radiotherapy on an MR-linac.
Materials And Methods:
We compared two MRI-guided MLC centroid tracking workflows, each using a different motion manager to derive and stream target positions to our in-house MLC tracking software. The first workflow relies on interleaved 2D (2.5D) cine-MRI, introducing minimal latency. In contrast, the second workflow utilized 3D cine-MRI, which operates at a relatively lower imaging frequency that introduces more latency.For experimental validation, we used a motion phantom equipped with an integrated insert that combines film with plastic scintillation dosimetry. A 2x12 Gy 11-beam prostate intensity modulated radiotherapy plan was created for tracking deliveries.
Results:
The signal latency introduced by the motion managers was 0.6 s for 2.5D cine-MRI and 6.3 s for 3D cine-MRI. Despite this latency, MLC tracking effectively restored the planned dose, improving the 2%/2mm local gamma pass-rates from 21% (due to linear drift) to 89% (2.5D) and 91% (3D). Plastic scintillator measurements showed reduced dose deviations at the periphery of the clinical target volume from 13-64% (no tracking) to 0-11% (2.5D) and 2-26% (3D).
Conclusion:
Our experiments demonstrated the technical feasibility of 2.5D and 3D cine-MRI-based MLC tracking on an MR-linac for 2-fraction prostate radiotherapy, with both motion management strategies achieving comparable dosimetric improvements despite the difference in latency.
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