Evidence map›Paper›PMID 39937363›Full record

ArticleDiscover oncology2025

Dynamic changes in peripheral blood immunophenotyping and its prognostic value in cervical cancer patients undergoing immune checkpoint blockade therapy.

Wenjian Gong, Zhi Wang, Yongqiang Wei, Maomao Wang, Kuina Li, Xiaoqi Chen, Xiaoling Huang, Lu Zhou, Qiuting Gan, Xiaoying Xu and 7 more

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

17 authors.

Wenjian Gong *National Clinical Research Center for Obstetrics and Gynecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Zhi Wang *Department of Gynecology and Obstetrics, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430014, China.
Yongqiang WeiDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Maomao WangDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Kuina LiDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Xiaoqi ChenDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Xiaoling HuangDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Lu ZhouDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Qiuting GanDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Xiaoying XuDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Zhijiong HuangDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Hongyu YaoDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Nengxian WuDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Lu HuangDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Bingbing YanDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China.
Bingbing ZhaoDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China. zhaobingbing@gxmu.edu.cn.
Zhijun YangDepartment of Obstetrics and Gynecology, Guangxi Medical University of Cancer Hospital, Nanning, 530021, Guangxi, China. yzj7528@126.com.

Funding

Guangxi medical appropriate health technology development and promotion project S20211019Natural Science Foundation of Guangxi Zhuang Autonomous Region 2023GXNSFAA026216
6 · The paper itself

Abstract

backgroundImmune checkpoint blockade (ICB) therapy, including antibodies targeting the programmed cell death protein 1 (PD-1) pathway, has significantly prolonged the overall survival (OS) in patients with advanced cervical cancer (CC). ICB treatment affects both target cells and various components released by immune cells, which can be observed in peripheral blood. However, there has been limited research on the dynamics of peripheral blood immunophenotyping and its association with OS in CC patients receiving ICB therapy.

methodsPatients with persistent, recurrent, or metastatic CC treated with ICB were enrolled between December 2019 and September 2022. The dynamic changes in peripheral blood immune cells, immunoglobulins, and complement components were analyzed at baseline (within 30 days prior to the first ICB cycle) and after the second cycle of ICB treatment (4-6 weeks after the first ICB treatment). Associations of the baseline levels of peripheral blood immune cells, immunoglobulins, complement components with OS were analyzed using multivariable Cox regression analysis.

resultsIn this retrospective cohort study, 119 patients who received at least two cycles of ICB were included. Data on peripheral blood immune cells, immunoglobulins, and complement components were available for 70 of these patients. The percentages of suppressor T (Ts) cells and natural killer (NK) cells in peripheral blood increased significantly post-ICB treatment, whereas the Th/Ts ratio and IgM levels decreased. The percentages of cytotoxic T (Tc) cells, Ts cells, the Th/Ts ratio, and levels of IgM, IgA, C3, and C4 were significantly associated with the OS of patients. Furthermore, multivariable Cox regression analysis found that a high level of IgA was associated with poor OS of the patients (HR = 2.918; 95% CI, 1.081-7.877, P = 0.035).

conclusionOur study demonstrated the potential proliferation of peripheral blood anti-tumor T cells in some CC patients undergoing ICB therapy. The observed associations between peripheral blood immunophenotyping and OS suggest that these biomarkers might have potential as prognostic tools.

Indexed as

Anti-PD-1Cervical cancerIgAPeripheral bloodTs cells

Identifiers

PMID39937363
PMCPMC11822146

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