Evidence map›Paper›PMID 41822509›Full record

ReviewFrontiers in immunology2026

Overcoming heterogeneity and immunosuppression: novel strategies in adoptive therapy for biliary tract cancer.

Yifan Zhu, Ge Xiong, Mingcheng Guan, Di Sun, Yanchao Guo, Jun Peng, Hong Zhu

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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

7 authors.

Yifan ZhuDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Ge XiongDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Mingcheng GuanDepartment of Medical Oncology, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu, China.
Di SunDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Yanchao GuoDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Jun PengDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Hong ZhuDepartment of Medical Oncology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Biliary tract cancer (BTC) is a highly heterogeneous malignancy originating from the biliary epithelium or gallbladder mucosa, characterized by strong invasiveness and poor prognosis. Although surgery remains the primary curative strategy, most patients are diagnosed at advanced stages, limiting surgical opportunities. The traditional gemcitabine plus cisplatin chemotherapy regimen, although a standard treatment, has limited efficacy and often leads to drug resistance. In recent years, adoptive cell immunotherapy has emerged as a promising new avenue for BTC treatment. Main body: This review systematically elaborates on the research progress of various ACT strategies in BTC, including chimeric antigen receptor T cells, tumor-infiltrating lymphocytes, natural killer cells, cytokine-induced killer cells, and T-cell receptor-engineered T cells. Furthermore, it comprehensively analyzes current key challenges and discusses future directions and optimization strategies regarding these therapies. Conclusion: This review summarizes recent progress in adoptive cell therapy for biliary tract cancer and discusses optimization strategies to facilitate clinical translation.

Indexed as

Biliary Tract NeoplasmsImmunotherapy, AdoptiveAnimalsHumansKiller Cells, NaturalLymphocytes, Tumor-InfiltratingReceptors, Chimeric AntigenT-LymphocytesReceptors, Chimeric Antigenadoptive cell immunotherapybiliary tract cancerchimeric antigen receptor T-cell therapycytokine-induced killer cellsnatural killer cellsT-cell receptor-engineered T cellstumor-infiltrating lymphocytes

Identifiers

PMID41822509
PMCPMC12975955

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.