Evidence map›Paper›PMID 39971854›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2025

Spatial organization of B lymphocytes and prognosis prediction in patients with gastric cancer.

Ryan Yong Kiat Tay, Manavi Sachdeva, Haoran Ma, Young-Woo Kim, Myeong-Cherl Kook, Hyunki Kim, Jae-Ho Cheong, Lindsay C Hewitt, Katharina Nekolla, Günter Schmidt and 12 more

Erratum issuedAbstract read
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Review
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Ryan Yong Kiat Tay *Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, Singapore, 119228, Singapore.
Manavi Sachdeva *Department of Haematology-Oncology, National University Cancer Institute, National University Hospital, Singapore, Singapore.
Haoran Ma *Cancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.
Young-Woo KimDepartment of Cancer Policy and Population Health, National Cancer Center Graduate School of Cancer Science and Policy and Center for Gastric Cancer and Department of Surgery, National Cancer Center, Goyang, Republic of Korea.
Myeong-Cherl KookCenter for Gastric Cancer, Department of Pathology, National Cancer Center, Goyang, Republic of Korea.
Hyunki KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jae-Ho CheongDepartment of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Lindsay C HewittDepartment of Pathology, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Center+, Maastricht, The Netherlands.
Katharina NekollaComputational Pathology, Oncology R&D, AstraZeneca, Munich, Germany.
Günter SchmidtComputational Pathology, Oncology R&D, AstraZeneca, Munich, Germany.
Takaki YoshikawaDepartment of Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Takashi OshimaDepartment of Surgery, Yokohama City University, Yokohama, Japan.
Tomio AraiDepartment of Pathology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Supriya SrivastavaDepartment of Medicine, National University of Singapore, Singapore, Singapore.
Ming TehDepartment of Pathology, National University Hospital, Singapore, Singapore.
Xuewen OngCancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.
Su Ting TayCancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.
Taotao ShengGenome Institute of Singapore, Agency for Science, Technology and Research, Singapore, Singapore.
Joseph J ZhaoYong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, Singapore, 119228, Singapore.
Patrick TanCancer and Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.
Heike I GrabschDepartment of Pathology, GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Center+, Maastricht, The Netherlands. h.grabsch@maastrichtuniversity.nl.
Raghav SundarYong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, Singapore, 119228, Singapore.ORCID 0000-0001-9423-1368

Funding

National Medical Research Council MOH-000967National Medical Research Council MOH-OFLCG18May-0003National Medical Research Council NMRC/CIRG23Jul-0035National Medical Research Council NMRC/ MOH-000627National University Health System Seed Fund NUHSRO/2024/008/RO5+6/Seed-Sep23/01National University Hospital Junior Research Award JRA/Sep23/002
6 · The paper itself

Abstract

backgroundWithin the tumor microenvironment (TME), the association of B lymphocytes (B cells) with prognosis and therapy response in gastric cancer (GC) remains poorly characterized. We investigated the predictive and prognostic value of B cells, including their spatial organization within the TME, in one of the largest multi-cohort studies to date.

methodsUsing CD20 immunohistochemistry, we evaluated B cell density in resection specimens from 977 patients with resectable GC across three cohorts, including the randomized phase III Korean CLASSIC trial. The relationship between CD20 density, clinicopathological characteristics, and overall survival (OS) was analyzed. Digital spatial profiling of 1063 regions of interest from 15 patients was performed to characterize B cell distribution within different regions of interest (ROIs) using the NanoString GeoMx platform.

resultsCD20 density was significantly higher in diffuse-type GC compared to intestinal-type (p = 0.000012). Patients with CD20-low diffuse-type GC had the shortest OS in the CLASSIC trial (median OS: 49 vs 62 months, HR: 1.9, 95% CI: 1.2-3.0, p = 0.003) and in a Japanese cohort (median OS: 49 vs 67 months, HR: 2.2, 95% CI: 1.2-4.0, p = 0.011). This survival difference was not seen in patients treated with adjuvant chemotherapy (median OS: 62 vs 63 months, HR: 1.8, 95% CI: 0.88-3.5, p = 0.108). Spatial profiling revealed significant B cell enrichment within tumor ROIs compared to the stroma, particularly in diffuse-type GC.

conclusionsLow CD20 positivity, especially in diffuse-type GC, is linked to poor prognosis and may identify patients who could benefit from chemotherapy. These findings underscore the role of B cells in GC.

Indexed as

B-LymphocytesStomach NeoplasmsTumor MicroenvironmentAdultAgedAntigens, CD20Biomarkers, TumorFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisSurvival RateAntigens, CD20Biomarkers, TumorB lymphocytesDigital Spatial ProfilingGastric cancerImmunohistochemistryTumor microenvironment

Identifiers

PMID39971854
PMCPMC11993452

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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.