Evidence map›Paper›PMID 37325934›Full record

ArticleCancer medicine2023

Genomic characterization between HER2-positive and negative gastric cancer patients in a prospective trial.

Qingjiang Hu, Eiji Oki, Teppei Yamada, Tomomi Kashiwada, Hideto Sonoda, Masato Kataoka, Hirofumi Kawanaka, Yasushi Tsuji, Akitaka Makiyama, Yuichiro Nakashima and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Circulating tumor DNA predicts clinical benefits of immune checkpoint blockade in HER2-negative patients with advanced gastric cancer.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
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  8. Assessing clinical pathological characteristics and gene expression patterns associated with hepatoid adenocarcinoma of the stomach.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

13 authors at 8 institutions in 1 country.

Qingjiang HuDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.ORCID 0000-0002-8313-5861
Eiji OkiDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.
Teppei YamadaDepartment of Gastroenterological Surgery, Fukuoka University Hospital, Fukuoka, Japan.
Tomomi KashiwadaDepartment of Medical Oncology, Saga Medical Center Koseikan, Saga, Japan.
Hideto SonodaImari Arita Kyoritsu Hospital, Nishimatsuura-gun, Japan.
Masato KataokaDepartment of Surgery, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Hirofumi KawanakaClinical Research Institute / Department of Gastroenterological Surgery, National Hospital Organization Beppu Medical Center, Beppu, Japan.
Yasushi TsujiDepartment of Medical Oncology, Tonan Hospital, Sapporo, Japan.
Akitaka MakiyamaCancer Center, Gifu University Hospital, Gifu, Japan.
Yuichiro NakashimaDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.
Mitsuhiko OtaDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.
Yasue KimuraDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.
Tomoharu YoshizumiDepartment of Surgery and Science, Kyushu University Hospital, Fukuoka, Japan.
Kyushu University Hospital · JPBeppu Medical Center · JPFukuoka University Hospital · JPGifu University Hospital · JPImari Arita Kyoritsu Hospital · JPNational Hospital Organization · JPSaga-Ken Medical Centre Koseikan · JPTonan Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to clarify the genomic characteristics of HER2-positive and negative gastric cancer cases that potentially affect tumor progression and treatment response in a prospective trial.

methodsWe collected 80 formalin-fixed paraffin-embedded (FFPE) samples (49 HER2+ and 31 HER2-) from gastric cancer patients who participated in the TROX-A1 trial (UMIN000036865). We queried a 435-gene panel (CANCERPLEX-JP) to generate comprehensive genomic profiling data, including the tumor mutation burden, somatic mutations, and copy number variations. In addition, the genomic differences between HER2+ and HER2- gastric cancer patients were analyzed.

resultsMutational analyses showed that TP53 was the most frequently mutated gene regardless of HER2 status. ARID1A mutation was significantly enriched in HER2-negative patients. The number of total mutations in HER2-negative patients with ARID1A mutation was remarkably higher than that in HER2-positive patients. Next, copy number variation analyses showed that the number of amplified genes (such as CCNE1, PGAP3, and CDK12) in HER2-positive cases was significantly higher than that in HER2-negative cases. Moreover, PTEN deletion was more common in HER2-positive cases. Finally, we found that, compared with HER2-positive patients, HER2-negative patients tended to have a higher tumor mutation burden, particularly in patients with ARID1A mutation. Pathway analyses of the gene alterations showed an enrichment of several immune-related pathways in HER2-negative patients.

conclusionsAccording to the genomic profiling of HER2-positive and negative gastric cancer, several gene alterations in the HER2 pathway may be the potential mechanism underlying trastuzumab resistance. Relative to HER2-positive gastric cancer, HER2-negative gastric tumors with ARID1A mutation may be sensitive to immune checkpoint inhibitors.

Indexed as

Stomach NeoplasmsDNA Copy Number VariationsErb-b2 Receptor Tyrosine KinasesGenomicsHumansMutationProspective StudiesTrastuzumabErb-b2 Receptor Tyrosine KinasesTrastuzumabbiomarkergastric cancergenomic profilingHER2TROX trial

Identifiers

PMID37325934
PMCPMC10469643
OpenAlexW4380871852

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.