Evidence map›Paper›PMID 41994009›Full record

ArticleESMO gastrointestinal oncology2026

Semiquantitative CLDN18 expression and clinical outcomes in patients with CLDN18-positive gastric cancer treated with zolbetuximab plus chemotherapy.

A Ooki, K Nakano, K Shimozaki, M Takamatsu, S Fukuoka, S Sakata, H Osumi, K Yoshikawa, E Toyokawa, K Yoshino and 7 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

17 authors.

A OokiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
K NakanoPathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
K ShimozakiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
M TakamatsuPathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
S FukuokaDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
S SakataPathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
H OsumiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
K YoshikawaDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
E ToyokawaDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
K YoshinoDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
S UdagawaDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
T WakatsukiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
M OguraDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
E ShinozakiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
K ChinDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.
H KawachiPathology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
K YamaguchiDepartments of Gastroenterological Chemotherapy, Japanese Foundation for Cancer Research, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Zolbetuximab plus chemotherapy improves survival in patients with human epidermal growth factor receptor 2 (HER2)-negative, claudin 18 (CLDN18)-positive advanced gastric cancer (AGC), which is defined as ≥75% of tumor cells with moderate-to-strong membranous staining. Whether semiquantitative expression within this range influences treatment outcomes is unknown. Patients and methods: This single-center retrospective study evaluated patients with AGC treated with zolbetuximab plus chemotherapy between July 2024 and September 2025. Tumors were independently reviewed by three pathologists and categorized as having moderate (75%-94%) or high (95%-100%) CLDN18 expression. Survival, response, and safety were compared across expression levels. Results: Fifty-one patients were included in the study. Baseline characteristics were similar across the groups. The median progression-free survival was 6.7 months in both expression groups, and the median overall survival was not reached. The objective response rates were 62.5% and 71.4%, and the disease control rates were 87.5% and 85.7% in the moderate and high expression groups, respectively. The depth of response (-33.6% versus -45.8%) and early tumor shrinkage (43.8% versus 71.4%) differed modestly. The profile of treatment-related adverse events was similar across the expression groups. Specimen type (biopsy or surgical resection) had no apparent impact on treatment outcomes. Conclusions: Within the approved CLDN18-positive threshold, the semiquantitative staining proportion showed no detectable differences in the efficacy or safety of zolbetuximab plus chemotherapy.

Indexed as

biomarkerclaudin 18gastric cancerzolbetuximab

Identifiers

PMID41994009
PMCPMC13080867

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