Evidence map›Paper›PMID 40467905›Full record

ArticleScientific reports2025

Location-specific analysis of clinicopathological characteristics and long-term prognosis of primary gastrointestinal diffuse large B-cell lymphoma.

Yunfu Feng, Sijie Zheng, Yibin Sun, Luojie Liu

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Heterogeneity in primary gastrointestinal DLBCL: from clinical management to molecular mechanisms and treatment strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yunfu FengDepartment of Endoscopy Center, The First People's Hospital of Kunshan, Suzhou, China.
Sijie ZhengDepartment of Endoscopy Center, The First People's Hospital of Kunshan, Suzhou, China.
Yibin SunDepartment of Gastroenterology, Suzhou Municipal Hospital, Gusu School, The Affiliated Suzhou Hospital of Nanjing Medical University, Nanjing Medical University, Suzhou, China.
Luojie LiuDepartment of Gastroenterology, Changshu Hospital Affiliated to Soochow University, Suzhou, China. luojieliu@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary gastrointestinal diffuse large B-cell lymphoma (PGI-DLBCL) is the most common lymphoma in the gastrointestinal tract, yet research on its clinicopathological characteristics and long-term prognosis across different sites is lacking. This study aims to assess these aspects in PGI-DLBCL patients using data from the Surveillance, Epidemiology, and End Results (SEER) database. Patients diagnosed with PGI-DLBCL between 2000 and 2021 were extracted from the SEER database. The clinicopathological characteristics of PGI-DLBCL in the stomach, small intestine, and colorectum were compared using Chi-square tests, and overall survival (OS) as well as cancer-specific survival (CSS) were evaluated using Kaplan-Meier curves and Cox regression analysis. A total of 10,935 patients were enrolled, with the stomach being the most prevalent site (53.3%), followed by the small intestine (26.3%) and colorectum (20.5%). Gastric PGI-DLBCL patients had higher proportions of elderly, females, and stage III/IV disease, primarily treated with chemotherapy. Patients with small intestine and colorectal PGI-DLBCL showed significantly better OS (HR 0.91, 95% CI 0.88-0.98, P = 0.021; HR 0.89, 95% CI 0.82-0.95, P < 0.001) and CSS (HR 0.93, 95% CI 0.81-0.98, P = 0.022; HR 0.86, 95% CI 0.78-0.94, P < 0.001) compared to gastric PGI-DLBCL. OS and CSS were similar between small intestine and colorectal PGI-DLBCL (P > 0.05). Five-year OS rates were 48.8%, 55.4%, and 52.8% for stomach, small intestine, and colorectum, respectively, with corresponding CSS rates of 61.5%, 65.6%, and 66.0%. Multivariate Cox regression identified age, race, marital status, tumor stage, location, and treatment as independent risk factors for OS and CSS. For gastric DLBCL, radiotherapy plus chemotherapy was most effective in improving prognosis, while surgery combined with chemotherapy was superior for small intestine and colorectal DLBCL. Gastric PGI-DLBCL has distinct clinicopathological features from small intestine and colorectum PGI-DLBCL, and may have a worse prognosis. However, chemoradiotherapy may enhance its outcome.

Indexed as

Gastrointestinal NeoplasmsLymphoma, Large B-Cell, DiffuseAdolescentAdultAgedAged, 80 and overFemaleHumansIntestine, SmallKaplan-Meier EstimateMaleMiddle AgedPrognosisSEER ProgramYoung AdultClinicopathological characteristicsPrimary gastrointestinal diffuse large B-cell lymphomaPrognosisSEER

Identifiers

PMID40467905
PMCPMC12137816

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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.