Evidence map›Paper›PMID 41531941›Full record

ArticleClinical and translational radiation oncology2026

Impact of tumour proximity to organs-at-risk in adaptive MR-guided SBRT for central lung tumours and metastases.

Sina Mansoorian, Ala Sami Ismail Salameh, Laura Hamm, Svenja Hering, Diego Kauffmann-Guerrero, Helmut Weingandt, Vanessa da Silva Mendes, Jan Hofmaier, Sebastian Marschner, Nina-Sophie Schmidt-Hegemann and 4 more

Abstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Sina MansoorianDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Ala Sami Ismail SalamehDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Laura HammDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Svenja HeringDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Diego Kauffmann-GuerreroDepartment of Medicine V, University Hospital, Munich, Munich, Germany.
Helmut WeingandtDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Vanessa da Silva MendesDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Jan HofmaierDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Sebastian MarschnerDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Nina-Sophie Schmidt-HegemannDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Guillaume LandryDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Claus BelkaDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Stefanie CorradiniDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Chukwuka EzeDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Centrally located lung tumours present challenges for SBRT due to elevated toxicity risk. Online adaptive MR-guided radiotherapy (oMRgRT) offers improved target coverage and Organ at risk (OAR) sparing by accounting for interfractional anatomical changes. This study evaluated the dosimetric impact of oMRgRT, with emphasis on tumour location relative to OARs and the clinical benefit of adaptation. Methods: We retrospectively analysed 36 PTVs across 294 treatment sessions using a 0.35 T MR-Linac. Tumours were categorised by proximity to six critical OARs: proximal bronchial tree (PBT), trachea, heart, great vessels, brachial plexus, and oesophagus. Predicted/reoptimised plans from all fractions were compared to assess improvements in target coverage and OAR sparing. All dosimetric parameters were presented as a percentage of baseline plan metrics. Statistical tests included the Wilcoxon signed-rank test and the Mann-Whitney Results: Adaptive planning significantly improved target volume dosimetry. PTV D Conclusion: Daily oMRgRT significantly improves target coverage and OAR sparing in centrally located tumours, especially in anatomically complex regions. The adaptive approach enables clinically meaningful trade-offs between tumour coverage and OAR sparing. Further studies are needed to refine adaptation protocols based on tumour sublocation.

Indexed as

Adaptive radiotherapyCentral lung tumoursMR-guided radiotherapyOrgan-at-risk sparingStereotactic body radiotherapy

Identifiers

PMID41531941
PMCPMC12794038

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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.