Evidence map›Paper›PMID 26883329›Full record

ArticleEuropean radiology2016

Restaging oesophageal cancer after neoadjuvant therapy with (18)F-FDG PET-CT: identifying interval metastases and predicting incurable disease at surgery.

John M Findlay, Richard S Gillies, James M Franklin, Eugene J Teoh, Greg E Jones, Sara di Carlo, Fergus V Gleeson, Nicholas D Maynard, Kevin M Bradley, Mark R Middleton

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Article in European radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 31 citations in OpenAlex.

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  9. Routinely staging gastric cancer withEuropean radiology · 2019
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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

10 authors at 1 institution in 1 country.

John M FindlayOxford OesophagoGastric Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LJ, UK. john.findlay@oncology.ox.ac.uk.
Richard S GilliesOxford OesophagoGastric Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LJ, UK.
James M FranklinDepartment of Nuclear Medicine, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LE, UK.
Eugene J TeohDepartment of Nuclear Medicine, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LE, UK.
Greg E JonesOxford OesophagoGastric Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LJ, UK.
Sara di CarloOxford OesophagoGastric Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LJ, UK.
Fergus V GleesonDepartment of Nuclear Medicine, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LE, UK.
Nicholas D MaynardOxford OesophagoGastric Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LJ, UK.
Kevin M BradleyDepartment of Nuclear Medicine, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LE, UK.
Mark R MiddletonNIHR Oxford Biomedical Research Centre, Churchill Hospital, Old Road, Headington, Oxford, OX3 7LE, UK.
Churchill Hospital · GB

Funding

Cancer Research UK 16466
6 · The paper itself

Abstract

objectivesIt is unknown whether restaging oesophageal cancer after neoadjuvant therapy with positron emission tomography-computed tomography (PET-CT) is more sensitive than contrast-enhanced CT for disease progression. We aimed to determine this and stratify risk.

methodsThis was a retrospective study of patients staged before neoadjuvant chemotherapy (NAC) by (18)F-FDG PET-CT and restaged with CT or PET-CT in a single centre (2006-2014).

resultsThree hundred and eighty-three patients were restaged (103 CT, 280 PET-CT). Incurable disease was detected by CT in 3 (2.91 %) and PET-CT in 17 (6.07 %). Despite restaging unsuspected incurable disease was encountered at surgery in 34/336 patients (10.1 %). PET-CT was more sensitive than CT (p = 0.005, McNemar's test). A new classification of FDG-avid nodal stage (mN) before NAC (plus tumour FDG-avid length) predicted subsequent progression, independent of conventional nodal stage. The presence of FDG-avid nodes after NAC and an impassable tumour stratified risk of incurable disease at surgery into high (75.0 %; both risk factors), medium (22.4 %; either), and low risk (3.87 %; neither) groups (p < 0.001). Decision theory supported restaging PET-CT.

conclusionsPET-CT is more sensitive than CT for detecting interval progression; however, it is insufficient in at least higher risk patients. mN stage and response (mNR) plus primary tumour characteristics can stratify this risk simply. KEY POINTS: • Restaging (18) F-FDG-PET-CT after neoadjuvant chemotherapy identifies metastases in 6 % of patients • Restaging (18) F-FDG-PET-CT is more sensitive than CT for detecting interval progression • Despite this, at surgery 10 % of patients had unsuspected incurable disease • New concepts (FDG-avid nodal stage and response) plus tumour impassability stratify risk • Higher risk (if not all) patients may benefit from additional restaging modalities.

Indexed as

AdultAgedChemotherapy, AdjuvantDecision TheoryDisease ProgressionEsophageal NeoplasmsEsophagectomyFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedNeoadjuvant TherapyNeoplasm MetastasisNeoplasm StagingPositron Emission Tomography Computed TomographyFluorodeoxyglucose F18RadiopharmaceuticalsCancer stagingComputed tomographyEsophageal cancerEsophagectomyPositron-emission tomography

Identifiers

PMID26883329
OpenAlexW2276729297

What OpenQuestion holds

Textmetadata
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.