Evidence map›Paper›PMID 38817664›Full record

ArticleWorld journal of gastroenterology2024

Immunotherapy for esophageal cancer: Where are we now and where can we go.

Yoshiaki Shoji, Kazuo Koyanagi, Kohei Kanamori, Kohei Tajima, Mika Ogimi, Yamato Ninomiya, Miho Yamamoto, Akihito Kazuno, Kazuhito Nabeshima, Takayuki Nishi and 1 more

Abstract readEditorial
In one paragraph

Article in World journal of gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  6. Mapping Two Decades of Research on Endoscopic Submucosal Dissection in Esophageal Cancer: A Bibliometric and Visual Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
  7. Article
  8. Harnessing biomarkers to guide immunotherapy in esophageal cancer: toward precision oncology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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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.

Yoshiaki ShojiDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Kazuo KoyanagiDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan. kkoyanagi@tsc.u-tokai.ac.jp.
Kohei KanamoriDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Kohei TajimaDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Mika OgimiDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Yamato NinomiyaDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Miho YamamotoDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Akihito KazunoDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Kazuhito NabeshimaDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Takayuki NishiDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Masaki MoriDepartment of Gastroenterological Surgery, Tokai University School of Medicine, Kanagawa 259-1193, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitor therapy has dramatically improved patient prognosis, and thereby transformed the treatment in various cancer types including esophageal squamous cell carcinoma (ESCC) in the past decade. Monoclonal antibodies that selectively inhibit programmed cell death-1 (PD-1) activity has now become standard of care in the treatment of ESCC in metastatic settings, and has a high expectation to provide clinical benefit during perioperative period. Further, anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) monoclonal antibody has also been approved in the treatment of recurrent/metastatic ESCC in combination with anti-PD-1 antibody. Well understanding of the existing evidence of immune-based treatments for ESCC, as well as recent clinical trials on various combinations with chemotherapy for different clinical settings including neoadjuvant, adjuvant, and metastatic diseases, may provide future prospects of ESCC treatment for better patient outcomes.

Indexed as

CTLA-4 AntigenEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaImmune Checkpoint InhibitorsImmunotherapyNeoadjuvant TherapyAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantHumansNeoplasm Recurrence, LocalPrognosisProgrammed Cell Death 1 ReceptorTreatment OutcomeCTLA-4 AntigenCTLA4 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorAdjuvant therapyAnti-cytotoxic T-lymphocyte–associated protein 4Clinical trialsCombination therapyEsophageal cancerImmune checkpoint inhibitorImmunotherapyNeoadjuvant therapyProgrammed cell death-1

Identifiers

PMID38817664
PMCPMC11135418

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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.