Evidence map›Paper›PMID 29776418›Full record

ArticleRadiation oncology (London, England)2018

The impact of contour variation on tumour control probability in anal cancer.

Michael P Jones, Jarad Martin, Kerwyn Foo, Patrick Estoesta, Lois Holloway, Michael Jameson

Abstract read
In one paragraph

Article in Radiation oncology (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Michael P JonesSchool of Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia. mpjones85@gmail.com.ORCID http://orcid.org/0000-0002-8377-5383
Jarad MartinSchool of Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia.
Kerwyn FooDepartment of Radiation Oncology, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
Patrick EstoestaDepartment of Radiation Oncology, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.
Lois HollowayLiverpool and Macarthur Cancer Therapy Centres, Liverpool, NSW, Australia.
Michael JamesonLiverpool and Macarthur Cancer Therapy Centres, Liverpool, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile intensity modulated radiotherapy (IMRT) has been widely adopted for the treatment of anal cancer (AC), the added contour complexity poses potential risks. This study investigates the impact of contour variation on tumour control probability (TCP) when using IMRT for AC.

methodsNine Australian centres contoured a single computed tomography dataset of a patient with AC. The same optimised template-based IMRT planning protocol was applied to each contour set to generate nine representative treatment plans and their corresponding dose volume histograms. A geometric analysis was performed on all contours. The TCP was calculated for each plan using the linear quadratic and logitEUD model.

resultsThe median concordance index (CI) for the bladder, head and neck of femur, bone marrow, small bowel and external genitalia was 0.94, 0.88, 0.84, 0.65 and 0.65, respectively. The median CI for the involved nodal, primary tumour and elective clinical target volumes were 0.85, 0.77 and 0.71, respectively. Across the nine plans, the TCP was not significantly different. Variation in TCP between plans increased as tumour cell load increased or radiation dose decreased.

conclusionsWhen using IMRT for AC, contour variations generated from a common protocol within the limits of minor deviations do not appear to have a significant impact on TCP. Contouring variations may be more critical with increasing tumour cell load or reducing radiotherapy dose.

Indexed as

AlgorithmsAnus NeoplasmsHumansOrgans at RiskRadiotherapy DosageRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedTumor BurdenAnal cancerChemo-radiotherapySquamous cell carcinomaTumour control probability

Identifiers

PMID29776418
PMCPMC5960192

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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.