Evidence map›Paper›PMID 40808532›Full record

ArticleCancer research and treatment2026

Clinicopathological Factors Influencing PD-L1 Expression and the Effect of Immune Checkpoint Inhibitors on Survival Outcomes in Patients with Gastric Cancer Depending on Sex in a Tertiary Hospital in South Korea.

Jeong Hwan Lee, Nayoung Kim, Ji-Hyun Kim, Hyeon Jeong Oh, Yeejin Kim, Yonghoon Choi, Hyemin Jo, Ho-Kyoung Lee, Jinju Choi, Yu Kyung Jun and 19 more

Abstract read
In one paragraph

Article in Cancer research and treatment, 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

29 authors.

Jeong Hwan LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Nayoung KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea. nakim49@snu.ac.kr.
Ji-Hyun KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Hyeon Jeong OhDepartment of Pathology, Seoul National University Bundang Hospital, Seongnam, Korea.
Yeejin KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yonghoon ChoiDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Hyemin JoDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Ho-Kyoung LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Jinju ChoiDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Yu Kyung JunDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Hyuk YoonDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Cheol Min ShinDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Young Soo ParkDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Dong Ho LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Hye Seung LeeDepartment of Pathology, Seoul National University College of Medicine, Seoul, Korea.
So Hyun KangDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Korea.
Young Suk ParkDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Korea.
Sang-Hoon AhnDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Korea.
Yun-Suhk SuhDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Korea.
Do Joong ParkDepartment of Surgery, Seoul National University College of Medicine, Seoul, Korea.
Hyung Ho KimDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Korea.
Ji-Won KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Jin Won KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Keun-Wook LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Won ChangDepartment of Radiology, Seoul National University Bundang Hospital, Seongnam, Korea.
Yoon Jin LeeDepartment of Radiology, Seoul National University Bundang Hospital, Seongnam, Korea.
Kyoung Ho LeeDepartment of Radiology, Seoul National University Bundang Hospital, Seongnam, Korea.
Young Hoon KimDepartment of Radiology, Seoul National University Bundang Hospital, Seongnam, Korea.
Soyeon AhnMedical Research Collaborating Center, Seoul National University Bundang Hospital, Seongnam, Korea.

Funding

Korea National Institute of Health 2025-ER1104-00Ministry of Science and ICTNational Research Foundation of Korea RS-2024-00337453
6 · The paper itself

Abstract

purposeProgrammed cell death ligand-1 (PD-L1) negatively regulates T-cell activation, and exhibits sex-based differences in expression and immune responses. This study investigated sex-related differences in clinicopathological factors influencing PD-L1 expression and the effect of immune checkpoint inhibitors (ICIs) on survival in gastric cancer (GC) patients in South Korea. MATERIALS AND

methodsWe analyzed a prospective cohort of 468 GC patients who underwent PD-L1 immunohistochemistry. Age, tumor characteristics, molecular features, and survival outcomes were compared by sex. Multivariate analyses, including Cox proportional hazards modeling with an interaction term for sex, were performed.

resultsAmong 468 patients, 280 (59.8%) were PD-L1 positive. In the overall cohort, PD-L1 positivity was significantly associated with Epstein-Barr virus (EBV) infection (odds ratio [OR], 7.46; p < 0.001), antral location of GC (OR, 1.84; p=0.027), and macrosatellite instability-high (MSI-H) (OR, 5.04; p=0.027). Diffuse-type histology was inversely associated (OR, 0.22; p=0.041). In males, EBV (OR, 36.27) and antral location (OR, 2.38) were significant. In females, only MSI-H was significant (OR, 11.63). ICI-containing therapy significantly improved survival in males (p=0.012) but not in females (p=0.415). Cox regression showed a survival benefit from ICIs (hazard ratio, 0.70; p=0.080), with a borderline-significant interaction by sex (p=0.073).

conclusionPD-L1 expression and therapeutic efficacy of ICIs differ by sex in GC. EBV infection and antral tumor location were independent factors in males, while MSI-H status was significant in females. These findings highlight the importance of sex-based immunobiology in tailoring GC treatment strategies.

Indexed as

B7-H1 AntigenImmune Checkpoint InhibitorsStomach NeoplasmsAdultAgedFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisProspective StudiesRepublic of KoreaSex FactorsTertiary Care CentersB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsB7-H1 antigenImmune checkpoint inhibitorsSexStomach neoplasmsSurvival

Identifiers

PMID40808532
PMCPMC13382561

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.