Evidence map›Paper›PMID 42452880›Full record

ReviewAnnals of medicine2026

Tertiary lymphoid structures in gastrointestinal cancer: orchestrating tumour microenvironmental immune subcycles to elegantly amplify the cancer immunity cycle.

Haobo Yin, Yuxi Qiao, Xiaoyan Li, Jingdong Zhang, Qian Dong

Abstract readReview
In one paragraph

Review in Annals of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Haobo YinMedical Oncology Department of Gastrointestinal Tumors, Liaoning Cancer Hospital & Institute, Cancer Hospital of China Medical University, Shenyang, China.ORCID 0009-0009-3614-3429
Yuxi QiaoMedical Oncology Department of Gastrointestinal Tumors, Liaoning Cancer Hospital & Institute, Cancer Hospital of China Medical University, Shenyang, China.
Xiaoyan LiPathology Department, Liaoning Cancer Hospital & Institute, Cancer Hospital of China Medical University, Cancer Hospital of Dalian University of Technology, Shenyang, China.
Jingdong ZhangMedical Oncology Department of Gastrointestinal Tumors, Liaoning Key Laboratory of Gastrointestinal Cancer Translational Research, Liaoning Cancer Hospital & Institute, Cancer Hospital of China Medical University, Cancer Hospital of Dalian University of Technology, Shenyang, China.ORCID 0000-0002-0711-2764
Qian DongMedical Oncology Department of Gastrointestinal Tumors, Liaoning Key Laboratory of Gastrointestinal Cancer Translational Research, Liaoning Cancer Hospital & Institute, Cancer Hospital of China Medical University, Cancer Hospital of Dalian University of Technology, Shenyang, China.ORCID 0000-0001-9810-1368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGastrointestinal (GI) cancers remain a major global health burden, with high incidence and mortality despite advances in multimodal therapies. Tertiary lymphoid structures (TLSs), ectopic lymphoid aggregates within the tumour microenvironment (TME), have emerged as key regulators of antitumour immunity and potential predictors of immunotherapy response. However, a focused synthesis of TLS biology specific to GI malignancies is still lacking.

methodsWe conducted a comprehensive narrative review of current literature to summarize the formation, maturation and functional roles of TLSs, with particular emphasis on their immunological and clinical relevance in GI cancers.

resultsTLSs structurally resemble secondary lymphoid organs and function as localized hubs for antigen presentation, lymphocyte recruitment and adaptive immune activation. In GI tumours, TLS presence, density and maturation status are closely associated with enhanced immune infiltration, improved prognosis and better response to immune checkpoint inhibitors. Emerging evidence also suggests that therapeutic interventions, including chemotherapy, radiotherapy and immunotherapy, may influence TLS formation and function. However, TLS heterogeneity and potential immunosuppressive components present challenges for their clinical application.

conclusionsTLSs represent promising biomarkers and therapeutic targets in GI oncology. While strategies to induce or modulate TLSs may enhance antitumour immunity, their clinical translation requires careful consideration of immune-related adverse effects and standardization of assessment methods. Integrating TLS-based approaches may advance precision immunotherapy in GI cancers.

Indexed as

Gastrointestinal NeoplasmsTertiary Lymphoid StructuresTumor MicroenvironmentAnimalsHumansImmune Checkpoint InhibitorsImmunotherapyPrognosisImmune Checkpoint Inhibitorscancer-immunity cyclegastrointestinal cancerspredictive biomarkersTertiary lymphoid structurestumour microenvironment

Identifiers

PMID42452880
PMCPMC13374757

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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.