Evidence map›Paper›PMID 41647975›Full record

ArticleESMO gastrointestinal oncology2025

Genomic heterogeneity and clinical implications in gastrointestinal neuroendocrine carcinoma:

T Ozato, Y Kono, H Yamamoto, A Hirasawa, D Ennishi, S Tomida, S Toyooka, M Otsuka

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

8 authors.

T OzatoDepartment of Gastroenterology and Hepatology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Hospital, Kita-ku, Okayama.
Y KonoDepartment of Gastroenterology and Hepatology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Hospital, Kita-ku, Okayama.
H YamamotoDepartment of Clinical Genomic Medicine, Okayama University Hospital, Kita-ku, Okayama.
A HirasawaDepartment of Clinical Genomic Medicine, Okayama University Hospital, Kita-ku, Okayama.
D EnnishiDepartment of Center for Comprehensive Genomic Medicine, Okayama University Hospital, Kita-ku, Okayama.
S TomidaDepartment of Center for Comprehensive Genomic Medicine, Okayama University Hospital, Kita-ku, Okayama.
S ToyookaDepartment of Center for Comprehensive Genomic Medicine, Okayama University Hospital, Kita-ku, Okayama.
M OtsukaDepartment of Gastroenterology and Hepatology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Hospital, Kita-ku, Okayama.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastrointestinal neuroendocrine carcinoma (GI-NEC) is a highly lethal malignancy with significant clinical and molecular heterogeneities. Given its rarity, large-scale studies are lacking, and research on its genomic landscape remains limited. Consequently, to date, no reliable biomarkers for treatment selection and prognosis have been identified. To address this gap in knowledge, we investigated the clinical impact of genomic features on GI-NEC. Methods: We retrospectively analyzed 261 patients with advanced or recurrent GI-NEC using a nationwide comprehensive genomic profiling database. We analyzed the correlation between platinum-based chemotherapy and the clinical outcomes in 152 patients, focusing on time to treatment failure and overall survival. We integrated the sequencing data with clinical information to identify potential biomarkers predictive of chemotherapy efficacy and survival. Results: In the GI-NECs analyzed, Conclusion: This study underscored the clinical and genomic heterogeneity of GI-NEC and highlighted the need to integrate genomic and clinical data to achieve personalized medicine.

Indexed as

comprehensive genomic profilinggastrointestinal neuroendocrine carcinomaKRAS alterationsMYC amplificationplatinum-based chemotherapy

Identifiers

PMID41647975
PMCPMC12836603

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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.