Evidence map›Paper›PMID 29465751›Full record

ArticleHistopathology2018

Prognostic value of pathological lymph node status and primary tumour regression grading following neoadjuvant chemotherapy - results from the MRC OE02 oesophageal cancer trial.

Nasser Davarzani, Gordon G A Hutchins, Nicholas P West, Lindsay C Hewitt, Matthew Nankivell, David Cunningham, William H Allum, Elizabeth Smyth, Nicola Valeri, Ruth E Langley and 1 more

Abstract read
In one paragraph

Article in Histopathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 4 pooled it
–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

27 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Prognostic relevance of lymph node regression on survival in esophageal cancer: a systematic review and meta-analysis.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2022
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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

11 authors.

Nasser DavarzaniGROW School for Oncology and Developmental Biology, Department of Pathology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Gordon G A HutchinsSection of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-1707-4415
Nicholas P WestSection of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
Lindsay C HewittGROW School for Oncology and Developmental Biology, Department of Pathology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Matthew NankivellMRC Clinical Trials Unit, University College London, London, UK.
David CunninghamGastrointestinal and Lymphoma Unit, Royal Marsden Hospital, London, UK.
William H AllumDepartment of Surgery, Royal Marsden Hospital, London, UK.
Elizabeth SmythGastrointestinal and Lymphoma Unit, Royal Marsden Hospital, London, UK.
Nicola ValeriGastrointestinal and Lymphoma Unit, Royal Marsden Hospital, London, UK.
Ruth E LangleyMRC Clinical Trials Unit, University College London, London, UK.
Heike I GrabschGROW School for Oncology and Developmental Biology, Department of Pathology, Maastricht University Medical Centre, Maastricht, the Netherlands.ORCID http://orcid.org/0000-0001-9520-6228

Funding

Cancer Research UK 18052Medical Research Council MC_U122861327Medical Research Council MC_UU_12023/28
6 · The paper itself

Abstract

aimsNeoadjuvant chemotherapy (NAC) remains an important therapeutic option for advanced oesophageal cancer (OC). Pathological tumour regression grade (TRG) may offer additional information by directing adjuvant treatment and/or follow-up but its clinical value remains unclear. We analysed the prognostic value of TRG and associated pathological factors in OC patients enrolled in the Medical Research Council (MRC) OE02 trial. METHODS AND

resultsHistopathology was reviewed in 497 resections from OE02 trial participants randomised to surgery (S group; n = 244) or NAC followed by surgery [chemotherapy plus surgery (CS) group; n = 253]. The association between TRG groups [responders (TRG1-3) versus non-responders (TRG4-5)], pathological lymph node (LN) status and overall survival (OS) was analysed. One hundred and ninety-five of 253 (77%) CS patients were classified as 'non-responders', with a significantly higher mortality risk compared to responders [hazard ratio (HR) = 1.53, 95% confidence interval (CI) = 1.05-2.24, P = 0.026]. OS was significantly better in patients without LN metastases irrespective of TRG [non-responders HR = 1.87, 95% CI = 1.33-2.63, P < 0.001 versus responders HR = 2.21, 95% CI = 1.11-4.10, P = 0.024]. In multivariate analyses, LN status was the only independent factor predictive of OS in CS patients (HR = 1.93, 95% CI = 1.42-2.62, P < 0.001). Exploratory subgroup analyses excluding radiotherapy-exposed patients (n = 48) showed similar prognostic outcomes.

conclusionLymph node status post-NAC is the most important prognostic factor in patients with resectable oesophageal cancer, irrespective of TRG. Potential clinical implications, e.g. adjuvant treatment or intensified follow-up, reinforce the importance of LN dissection for staging and prognostication.

Indexed as

AdultAgedChemotherapy, AdjuvantEsophageal NeoplasmsFemaleHumansLymphatic MetastasisLymph NodesMaleMiddle AgedNeoadjuvant TherapyNeoplasm GradingPrognosisneoadjuvant chemotherapyoesophageal carcinomatumour regression grade

Identifiers

PMID29465751
PMCPMC5969086

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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.