Evidence map›Paper›PMID 41699916›Full record

ArticleThe British journal of surgery2026

Survival after pathological complete response following neoadjuvant chemotherapy versus chemoradiotherapy for oesophageal squamous cell carcinoma.

Jun Okui, Satoru Matsuda, Kengo Nagashima, Yasunori Sato, Hirofumi Kawakubo, Thomas Ruhstaller, Peter Thuss-Patience, Magnus Nilsson, Fredrik Klevebro, Lijie Tan and 10 more

Abstract readComparative Study
In one paragraph

Article in The British journal of surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  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

20 authors.

Jun OkuiDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-5226-1347
Satoru MatsudaDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0001-8441-2755
Kengo NagashimaBiostatistics Unit, Clinical and Translational Research Center, Keio University Hospital, Tokyo, Japan.ORCID 0000-0003-4529-9045
Yasunori SatoDepartment of Biostatistics, Keio University School of Medicine, Tokyo, Japan.
Hirofumi KawakuboDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-4929-5482
Thomas RuhstallerCompetence Center, Swiss Cancer Institute, Bern, Switzerland.
Peter Thuss-PatienceDepartment of Haematology, Oncology, and Cancer Immunology, Charité-University Medicine Berlin, Campus Virchow Klinikum, Berlin, Germany.ORCID 0000-0002-8544-9872
Magnus NilssonDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-6215-8132
Fredrik KlevebroDepartment of Upper Abdominal Diseases, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-1695-4103
Lijie TanDepartment of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-0708-5556
Shaoyuan ZhangDepartment of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-6187-4313
Thomas AparicioDepartment of Digestive Oncology, Hôpital Saint-Louis, APHP, Université Paris Cité, Paris, France.ORCID 0000-0001-8834-6927
Guillaume PiessenUMR9020-U1277-CANTHER-Cancer Heterogeneity, Plasticity, and Resistance to Therapies, University Lille, CNRS, Inserm, CHU Lille, Lille, France.ORCID 0000-0001-8243-8310
Charlène van der ZijdenDepartment of Surgery, Erasmus MC Cancer Institute, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0002-3650-8303
Bianca MostertDepartment of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0001-5193-0820
Bas P L WijnhovenDepartment of Surgery, Erasmus MC Cancer Institute, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0003-4738-3697
Takahiro TsushimaDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan.ORCID 0000-0003-3551-7504
Hiroya TakeuchiDepartment of Surgery, Hamamatsu University School of Medicine, Shizuoka, Japan.ORCID 0000-0002-3947-0128
Ken KatoDepartment of Head and Neck, Oesophageal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-1733-5072
Yuko KitagawaDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0001-6469-2155

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough several oesophageal squamous cell carcinoma (OSCC) studies have reported no definitive overall survival (OS) differences between neoadjuvant chemoradiotherapy (NACRT) and neoadjuvant chemotherapy (NAC), the higher pCR rate with NACRT has been viewed as a potential advantage. Beyond ongoing concerns about the validity of pCR as a surrogate endpoint, it remains uncertain whether survival differs between these modalities among patients with OSCC who achieve pCR.

methodsAn integrated analysis of individual patient data (IPD) from phase III trials evaluating perioperative therapies for resectable OSCC was conducted, emphasizing prognostic differences between NAC and NACRT, particularly among patients who achieved pCR.

resultsIPD from seven phase III RCTs across six countries included data for 1044 patients with OSCC (83.5% male; mean age of 62.3 years). Of these patients, 605 (58.0%) received NAC and 439 (42.0%) received NACRT, with R0 resection rates of 89.6% versus 84.7% and pCR rates of 6.9% versus 34.2% respectively. Among patients who achieved pCR (192 patients), 5-year OS was 97.5% in the NAC group and 70.4% in the NACRT group, while 5-year recurrence-free survival was 80.8% and 63.7% respectively. Multivariable analysis demonstrated a significant survival advantage for NAC among patients who achieved pCR.

conclusionAmong patients who achieved pCR, postoperative outcomes varied considerably by neoadjuvant treatment modality. The markedly favourable prognosis associated with pCR after NAC suggests that these patients may represent an optimal candidate cohort for future evaluation of surgery-avoidance and watch-and-wait strategies.

Indexed as

Carcinoma, Squamous CellChemoradiotherapyChemoradiotherapy, AdjuvantEsophageal NeoplasmsNeoadjuvant TherapyChemotherapy, AdjuvantClinical Trials, Phase III as TopicEsophageal Squamous Cell CarcinomaFemaleHumansMaleMiddle AgedPathologic Complete ResponsePrognosisRandomized Controlled Trials as TopicTreatment Outcome

Identifiers

PMID41699916
PMCPMC13017761

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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.