Evidence map›Paper›PMID 41708962›Full record

ArticleDiscover oncology2026

Higher frequency of circulating regulatory T cells is associated with poor outcomes in patients with colorectal cancer.

Yan Lu, Haoyang Guo, Taotao Guo, Longyi Zhang, Xinling Pan

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yan LuClinical Laboratory, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China. luyan11219@wmu.edu.cn.
Haoyang GuoClinical Laboratory, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China.
Taotao GuoDepartment of Reproductive Center, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China.
Longyi ZhangClinical Laboratory, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China.
Xinling PanDepartment of Biomedical Sciences Laboratory, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China. panfengyuwuzu@163.com.

Funding

Jinhua Science and Technology Bureau 2023-3-018
6 · The paper itself

Abstract

backgroundWhile immune dysregulation significantly influences colorectal cancer (CRC) progression, this study aimed to investigate the levels of circulating regulatory T cells (cTreg) and their subsets, follicular helper T cells (cTfh), and follicular regulatory T cells (cTfr) in patients with CRC and to evaluate their prognostic significance.

methodsWe enrolled 120 patients with CRC (January 2021 to September 2022) and 91 healthy controls (HCs). Flow cytometry was used to quantify the frequency of cTregs and their subsets (resting Tregs/activated Tregs), cTfh, and cTfr. Patients were prospectively followed up until April 2025, with overall survival (OS) as the primary endpoint. Univariable and multivariable Cox proportional hazards models were employed to identify significant prognostic factors for OS. Survival curves were generated using the Kaplan-Meier method and compared with the log-rank test.

resultsAfter a 35-month median follow-up, 22 patients with CRC had died (18.3% mortality rate). Patients with CRC had higher cTreg (7.43% vs. 6.33%, P < 0.001), cTfh (15.8% vs. 13.8%, P < 0.001), and cTfr (2.39% vs. 2.20%, P = 0.019) than HCs. Patients with advanced-stage CRC had higher cTreg levels than those with early-stage CRC (7.68% vs. 7.10%, P = 0.006). Higher frequency of cTreg levels (≥ 8.295%, area under the curve = 0.717) was correlated with shorter OS.

conclusionscTreg, cTfh, and cTfr levels are elevated in patients with CRC. An elevated cTreg frequency is associated with poor CRC prognosis. Assessment of cTreg levels may aid in prognostic assessment.

Indexed as

Circulating regulatory T cellsColorectal cancerFollicular helper T cellsFollicular regulatory T cellsPrognosis

Identifiers

PMID41708962
PMCPMC13022075

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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.