Evidence map›Paper›PMID 42158315›Full record

ArticlePhysics and imaging in radiation oncology2026

In-vivo dosimetry using electronic portal imaging in online-adaptive radiotherapy for rectal cancer.

Gary Razinskas, Robert Schindhelm, Anne Richter, Johannes Kraft, Marcus Zimmermann, Jörg Tamihardja, Andrea Wittig-Sauerwein, Sonja Wegener

Abstract read
In one paragraph

Article in Physics and imaging in radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Gary RazinskasUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Robert SchindhelmUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Anne RichterUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Johannes KraftUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Marcus ZimmermannUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Jörg TamihardjaUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Andrea Wittig-SauerweinUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.
Sonja WegenerUniversity Hospital Würzburg, Department of Radiotherapy and Radiation Oncology, Josef-Schneider-Str. 11, 97080 Würzburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: Electronic portal imaging device (EPID)-based in-vivo dosimetry (IVD) is widely used to verify radiotherapy dose delivery and detect deviations from anatomical changes, setup uncertainties, or machine-related errors. However, cone-beam computed tomography (CBCT)-guided online-adaptive radiotherapy (oART), which re-optimizes treatment plans on-couch based on daily imaging, lacks a measurement-based quality assurance framework. This study aimed to evaluate the feasibility and accuracy of EPID-based transit IVD for CBCT-based oART. Materials and methods: EPID-based IVD data from ten patients receiving short-course oART for rectal cancer on an Ethos linear accelerator were retrospectively analyzed over 50 treatment sessions using a commercial EPID-based IVD framework. Gamma pass rates (GPR) were calculated using global gamma criteria of 3 %/3 mm, 3 %/2 mm, and 2 %/2 mm. Angular dependence and field shape effects were investigated using in-air and in-phantom measurements. Results: Across all patients and fractions, the mean GPR at 3 %/3 mm with a 20 % low-dose threshold was (95.7 ± 1.8) %, with patient-specific means ranging from 91.4 % to 98.0 %. Two sessions showed notable reductions associated with large intra-fractional gas variations. Angular analysis revealed notable GPR variations, particularly for laterally incident fields. Conclusions: EPID-based IVD was a promising quality assurance approach for verifying oART delivery, achieving higher GPRs under tighter evaluation criteria than typically reported for standard image-guided radiotherapy. These findings indicate that workflow-specific tolerance criteria should be defined to reflect the reduced anatomical variation in adaptive treatments, requiring more accurate beam modeling. Automating EPID-based IVD integration into clinical protocols will be essential for safe and efficient implementation.

Indexed as

Electronic portal imaging deviceIn-vivo dosimetryOnline-adaptive radiotherapy

Identifiers

PMID42158315
PMCPMC13181284

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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.