Evidence map›Paper›PMID 35264184›Full record

ArticleRadiation oncology (London, England)2022

Quantification of biological range uncertainties in patients treated at the Krakow proton therapy centre.

Magdalena Garbacz, Jan Gajewski, Marco Durante, Kamil Kisielewicz, Nils Krah, Renata Kopeć, Paweł Olko, Vincenzo Patera, Ilaria Rinaldi, Marzena Rydygier and 6 more

Abstract read
In one paragraph

Article in Radiation oncology (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

16 authors.

Magdalena GarbaczInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland. magdalena.garbacz@ifj.edu.pl.ORCID http://orcid.org/0000-0002-3522-0025
Jan GajewskiInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland.
Marco DuranteGSI Helmholtzzentrum fur Schwerionenforschung, 64291, Darmstadt, Germany.
Kamil KisielewiczNational Oncology Institute, National Research Institute, Krakow Branch, 31115, Kraków, Poland.
Nils KrahUniversity of Lyon, CREATIS, CNRS UMR5220, Inserm U1044, INSA-Lyon, Université Lyon 1, Centre Léon Bérard, France.
Renata KopećInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland.
Paweł OlkoInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland.
Vincenzo PateraINFN - Section of Rome, 00185, Rome, Italy.
Ilaria RinaldiZonPTC/Maastro Clinic, Maastricht, The Netherlands.
Marzena RydygierInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland.
Angelo SchiaviINFN - Section of Rome, 00185, Rome, Italy.
Emanuele ScifoniTrento Institute for Fundamental Physics and Applications, TIFPA-INFN, 38123, Povo, Trento, Italy.
Tomasz SkóraNational Oncology Institute, National Research Institute, Krakow Branch, 31115, Kraków, Poland.
Agata SkrzypekAwesome Industries Solutions, 31026, Kraków, Poland.
Francesco TommasinoTrento Institute for Fundamental Physics and Applications, TIFPA-INFN, 38123, Povo, Trento, Italy.
Antoni RucinskiInstitute of Nuclear Physics Polish Academy of Sciences, 31342, Kraków, Poland.

Funding

fundacja na rzecz nauki polskiej POIR.04.04.00-00-2475/16-00narodowe centrum badań i rozwoju POWR.03.02.00-00-I013/16
6 · The paper itself

Abstract

backgroundVariable relative biological effectiveness (vRBE) in proton therapy might significantly modify the prediction of RBE-weighted dose delivered to a patient during proton therapy. In this study we will present a method to quantify the biological range extension of the proton beam, which results from the application of vRBE approach in RBE-weighted dose calculation. METHODS AND MATERIALS: The treatment plans of 95 patients (brain and skull base patients) were used for RBE-weighted dose calculation with constant and the McNamara RBE model. For this purpose the Monte Carlo tool FRED was used. The RBE-weighted dose distributions were analysed using indices from dose-volume histograms. We used the volumes receiving at least 95% of the prescribed dose (V95) to estimate the biological range extension resulting from vRBE approach.

resultsThe vRBE model shows higher median value of relative deposited dose and D95 in the planning target volume by around 1% for brain patients and 4% for skull base patients. The maximum doses in organs at risk calculated with vRBE was up to 14 Gy above dose limit. The mean biological range extension was greater than 0.4 cm. DISCUSSION: Our method of estimation of biological range extension is insensitive for dose inhomogeneities and can be easily used for different proton plans with intensity-modulated proton therapy (IMPT) optimization. Using volumes instead of dose profiles, which is the common method, is more universal. However it was tested only for IMPT plans on fields arranged around the tumor area.

conclusionsAdopting a vRBE model results in an increase in dose and an extension of the beam range, which is especially disadvantageous in cancers close to organs at risk. Our results support the need to re-optimization of proton treatment plans when considering vRBE.

Indexed as

Brain NeoplasmsFemaleHumansMaleMonte Carlo MethodNeoplasm StagingOrgans at RiskPolandProton TherapyRadiotherapy DosageRadiotherapy Planning, Computer-AssistedRelative Biological EffectivenessSkull Base NeoplasmsTomography, X-Ray ComputedBiological range extensionMonte CarloProton therapyRange uncertaintiesVariable RBE

Identifiers

PMID35264184
PMCPMC8905899

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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.