Evidence map›Paper›PMID 37393217›Full record

ArticleJournal of gastrointestinal cancer2024

D C van der Aa, S S Gisbertz, M C J Anderegg, S M Lagarde, R Klaassen, S L Meijer, S van Dieren, McCm Hulshof, Jjghm Bergman, R J Bennink and 2 more

Abstract read
In one paragraph

Article in Journal of gastrointestinal cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

D C van der AaDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
S S GisbertzDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
M C J AndereggDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
S M LagardeDepartment of Surgery, Erasmus Medical Center, Rotterdam, Netherlands.
R KlaassenDepartment of Medical Oncology, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
S L MeijerDepartment of Pathology, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
S van DierenDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
McCm HulshofDepartment of Radiotherapy, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
Jjghm BergmanDepartment of Gastroenterology, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
R J BenninkDepartment of Radiology and Nuclear Medicine, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands.
H W M van LaarhovenCancer Treatment and Quality of Life, Cancer Center Amsterdam, Amsterdam, Netherlands.
M I van Berge HenegouwenDepartment of Surgery, Amsterdam UMC, location University of Amsterdam, Amsterdam, Netherlands. m.i.vanbergehenegouwen@amsterdamumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe curative strategy for patients with esophageal cancer without distant metastases consists of esophagectomy with preceding chemo(radio)therapy (CRT). In 10-40% of patients treated with CRT, no viable tumor is detectable in the resection specimen (pathological complete response (pCR)). This study aims to define the clinical outcomes of patients with a pCR and to assess the accuracy of post-CRT FDG-PET/CT in the detection of a pCR.

methodsFour hundred sixty-three patients with cancer of the esophagus or gastroesophageal junction who underwent esophageal resection after CRT between 1994 and 2013 were included. Patients were categorized as pathological complete responders or noncomplete responders. Standardized uptake value (SUV) ratios of 135 post-CRT FDG-PET/CTs were calculated and compared with the pathological findings in the corresponding resection specimens.

resultsOf the 463 included patients, 85 (18.4%) patients had a pCR. During follow-up, 25 (29.4%) of these 85 patients developed recurrent disease. Both 5-year disease-free survival (5y-DFS) and 5-year overall survival (5y-OS) were significantly higher in complete responders compared to noncomplete responders (5y-DFS 69.6% vs. 44.2%; P = 0.001 and 5y-OS 66.5% vs. 43.7%; P = 0.001). Not pCR, but only pN0 was identified as an independent predictor of (disease-free) survival.

conclusionPatients with a pCR have a higher probability of survival compared to noncomplete responders. One third of patients with a pCR do develop recurrent disease, and pCR can therefore not be equated with cure. FDG-PET/CT was inaccurate to predict pCR and therefore cannot be used as a sole diagnostic tool to predict pCR after CRT for esophageal cancer.

Indexed as

Esophageal NeoplasmsEsophagogastric JunctionFluorodeoxyglucose F18Neoadjuvant TherapyPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overDisease-Free SurvivalEsophagectomyFemaleFollow-Up StudiesHumansMaleMiddle AgedRadiopharmaceuticalsFluorodeoxyglucose F18RadiopharmaceuticalsComplete pathologic responseEsophageal cancerPrediction

Identifiers

PMID37393217
PMCPMC11096198

What OpenQuestion holds

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Registered trials

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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.