Evidence map›Paper›PMID 37924344›Full record

ArticleEuropean radiology2024

Training and external validation of pre-treatment FDG PET-CT-based models for outcome prediction in anal squamous cell carcinoma.

Russell Frood, Joseph Mercer, Peter Brown, Ane Appelt, Hitesh Mistry, Rohit Kochhar, Andrew Scarsbrook

Open access · hybridAbstract readValidation StudyMulticenter Study
In one paragraph

Article in European radiology, 2024. 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
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. A machine learning approach usingFrontiers in immunology · 2024
    Article
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 5 institutions in 1 country.

Russell FroodDepartment of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK. russellfrood@nhs.net.ORCID http://orcid.org/0000-0003-2681-9922
Joseph MercerDepartment of Radiology, The Christie NHS Foundation Trust, Manchester, UK.
Peter BrownDepartment of Radiology, York and Scarborough Teaching Hospitals NHS Foundation Trust, York, UK.
Ane AppeltLeeds Institute of Medical Research at St James's, University of Leeds, Leeds, UK.
Hitesh MistryDivision of Pharmacy, University of Manchester, Manchester, UK.
Rohit KochharDepartment of Radiology, The Christie NHS Foundation Trust, Manchester, UK.
Andrew ScarsbrookDepartment of Radiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
The Christie NHS Foundation Trust · GBUniversity of Leeds · GBLeeds Teaching Hospitals NHS Trust · GBUniversity of Manchester · GBYork Teaching Hospital NHS Foundation Trust · GB

Funding

Cancer Research UK 28832Cancer Research UK C19942/A28832Cancer Research UK RCCCTF-OCT22/100002Wellcome Trust 104688
6 · The paper itself

Abstract

objectivesThe incidence of anal squamous cell carcinoma (ASCC) is increasing worldwide, with a significant proportion of patients treated with curative intent having recurrence. The ability to accurately predict progression-free survival (PFS) and overall survival (OS) would allow for development of personalised treatment strategies. The aim of the study was to train and external test radiomic/clinical feature derived time-to-event prediction models.

methodsConsecutive patients with ASCC treated with curative intent at two large tertiary referral centres with baseline FDG PET-CT were included. Radiomic feature extraction was performed using LIFEx software on the pre-treatment PET-CT. Two distinct predictive models for PFS and OS were trained and tuned at each of the centres, with the best performing models externally tested on the other centres' patient cohort.

resultsA total of 187 patients were included from centre 1 (mean age 61.6 ± 11.5 years, median follow up 30 months, PFS events = 57/187, OS events = 46/187) and 257 patients were included from centre 2 (mean age 62.6 ± 12.3 years, median follow up 35 months, PFS events = 70/257, OS events = 54/257). The best performing model for PFS and OS was achieved using a Cox regression model based on age and metabolic tumour volume (MTV) with a training c-index of 0.7 and an external testing c-index of 0.7 (standard error = 0.4).

conclusionsA combination of patient age and MTV has been demonstrated using external validation to have the potential to predict OS and PFS in ASCC patients. CLINICAL RELEVANCE STATEMENT: A Cox regression model using patients' age and metabolic tumour volume showed good predictive potential for progression-free survival in external testing. The benefits of a previous radiomics model published by our group could not be confirmed on external testing. KEY POINTS: • A predictive model based on patient age and metabolic tumour volume showed potential to predict overall survival and progression-free survival and was validated on an external test cohort. • The methodology used to create a predictive model from age and metabolic tumour volume was repeatable using external cohort data. • The predictive ability of positron emission tomography-computed tomography-derived radiomic features diminished when the influence of metabolic tumour volume was accounted for.

Indexed as

Anus NeoplasmsCarcinoma, Squamous CellFluorodeoxyglucose F18Positron Emission Tomography Computed TomographyRadiopharmaceuticalsAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesFluorodeoxyglucose F18RadiopharmaceuticalsAnal canalEvent-free survivalPositron emission tomography computed tomographySquamous cell carcinoma

Identifiers

PMID37924344
PMCPMC11126458
OpenAlexW4388341484

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.