Evidence map›Paper›PMID 26968827›Full record

ArticleRadiation oncology (London, England)2016

Short-course PET based simultaneous integrated boost for locally advanced cervical cancer.

Marius Røthe Arnesen, Bernt Louni Rekstad, Caroline Stokke, Kjersti Bruheim, Ayca Muftuler Løndalen, Taran Paulsen Hellebust, Eirik Malinen

Open access · goldAbstract read
In one paragraph

Article in Radiation oncology (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  4. Use of BaselineFrontiers in oncology · 2020
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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

7 authors at 1 institution in 1 country.

Marius Røthe ArnesenDepartment of Medical Physics, The Norwegian Radium Hospital, Oslo University Hospital, PO Box 4953, Nydalen, N-0424, Oslo, Norway. mariua@ous-hf.no.ORCID http://orcid.org/0000-0001-8609-6477
Bernt Louni RekstadDepartment of Medical Physics, The Norwegian Radium Hospital, Oslo University Hospital, PO Box 4953, Nydalen, N-0424, Oslo, Norway.
Caroline StokkeThe Intervention Centre, Oslo University Hospital, Oslo, Norway.
Kjersti BruheimDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Ayca Muftuler LøndalenDepartment of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.
Taran Paulsen HellebustDepartment of Medical Physics, The Norwegian Radium Hospital, Oslo University Hospital, PO Box 4953, Nydalen, N-0424, Oslo, Norway.
Eirik MalinenDepartment of Medical Physics, The Norwegian Radium Hospital, Oslo University Hospital, PO Box 4953, Nydalen, N-0424, Oslo, Norway.
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with large, locally advanced cervical cancers (LACC) are challenging to treat. The purpose of this work is to use 18F-FDG PET as planning basis for a short-course simultaneous integrated boost (SIB) in external beam radiotherapy of LACC in order to increase tumour shrinkage and likelihood of local control.

methodsTen previously treated patients with LACC were included, all with pre-treatment FDG PET/CT images available. The FDG avid tumour volume, MTV50, was dose escalated in silico by intensity modulated radiotherapy from the standard 1.8 Gy to 2.8 Gy per fraction for the 10 first fractions; a short-course SIB. For the 18 remaining external fractions, standard pelvic treatment followed to total PTV and MTV50 doses of 50.4 Gy and 60.4 Gy, respectively. Photon and proton treatment were considered using volumetric modulated arc treatment (VMAT) and intensity-modulated proton therapy (IMPT), respectively. All treatment plans were generated using the Eclipse Treatment Planning System (TPS). The impact of tumour shrinkage on doses to organs at risk (OARs) was simulated in the TPS for the SIB plans.

resultsDose escalation could be implemented using both VMAT and IMPT, with a D98 ≥ 95 % for MTV50 being achieved in all cases. The sum of the 10 fraction short-course SIB and subsequent 18 standard fractions was compared to the standard non-SIB approach by dose volume histogram (DVH) analysis. Only marginal increase of dose to OARs was found for both modalities and a small further increase estimated from tumour shrinkage. Most DVH parameters showed a mean difference below 2 %. IMPT had, compared to VMAT, reduced OAR doses in the low to intermediate dose range, but showed no additional advantage in dose escalation.

conclusionsPlanning of dose escalation based on a FDG avid boost volume was here demonstrated feasible. The concept may allow time for enhanced tumour shrinkage before brachytherapy. Thus, this strategy may prove clinically valuable, in particular for patients with large tumours.

Indexed as

Positron-Emission TomographyAdultAgedComputer SimulationFemaleFluorodeoxyglucose F18HumansMiddle AgedOrgans at RiskPhotonsProton TherapyRadiotherapyRadiotherapy DosageRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedRetrospective StudiesFluorodeoxyglucose F18BrachytherapyCervical cancerDose escalationDose paintingPETRadiotherapySIB

Identifiers

PMID26968827
PMCPMC4788887
OpenAlexW2293958501

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.