Evidence map›Paper›PMID 40781322›Full record

ArticleRadiation oncology (London, England)2025

From standardized to individualized margins for online adaptive tumor dose escalation in rectal cancer.

C M Kensen, Lisa Wiersema, Anja Betgen, Doenja M J Lambregts, Corrie A M Marijnen, Uulke A van der Heide, Tomas M Janssen

Abstract read
In one paragraph

Article in Radiation oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

C M KensenDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Lisa WiersemaDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Anja BetgenDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Doenja M J LambregtsDepartment of Radiology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Corrie A M MarijnenDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Uulke A van der HeideDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands.
Tomas M JanssenDepartment of Radiation Oncology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, 1066 CX, The Netherlands. t.janssen@nki.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo determine the impact of tumor characteristics such as tumor volume, circumference and location in the rectum on intrafraction motion during dose-escalated MRI-guided radiotherapy of rectal cancer and to explore the potential of PTV margin individualization.

methodsSeventy-seven rectal cancer patients, treated with short course radiotherapy (SCRT) on a 1.5T MR-Linac, were included in the study. For all five treatment fractions per patient, the GTV of the primary tumor was manually delineated on T2-weighted images acquired for online plan adaptation (MRI

resultsIntrafraction motion was correlated with tumor location with larger displacement in Anterior-Posterior (p = 0.001) and Cranial-Caudal (CC; p = 0.043) direction for caudal tumors compared to proximal tumors (lower border starting > 5 cm from anorectal junction). For tumor volume, a significant (p = 0.049), but small association with Left-Right motion was found, with larger tumors exhibiting larger motion. PTV margins required for the full cohort were 2.8 mm LR, 6.3 mm AP, 2.2 mm cranial and 5.6 mm caudal. Individualizing on tumor location resulted in AP margin of 3.5 mm for proximal rectal tumors and 6.7 mm for distal rectal tumors. Margins in CC direction were 3.2 mm for proximal rectal tumors and asymmetrically 2.0 mm cranial and 6.0 mm caudal for distal rectal tumors.

conclusionOur study demonstrated that distance to anorectal junction significantly influenced the magnitude and direction of the intrafraction motion of rectal cancer patients receiving SCRT, with distal tumors showing larger motion in the AP and CC directions. For proximal rectal tumors, the margin could be decreased in AP and CC direction.

Indexed as

Radiotherapy, Image-GuidedRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedRectal NeoplasmsAdultAgedAged, 80 and overDose Fractionation, RadiationFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPrognosisRadiotherapy DosageTumor BurdenIndividualized marginsIntrafraction motionMRI-guided radiotherapyOnline adaptive radiotherapyPTV marginRectal cancer

Identifiers

PMID40781322
PMCPMC12335123

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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.