Evidence map›Paper›PMID 37364934›Full record

ArticleJournal for immunotherapy of cancer2023

Characterization of intratumoral tertiary lymphoid structures in pancreatic ductal adenocarcinoma: cellular properties and prognostic significance.

Xuan Zou, Xuan Lin, He Cheng, Yusheng Chen, Ruijie Wang, Mingjian Ma, Yu Liu, Zhengjie Dai, Yesboli Tasiheng, Yu Yan and 6 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
–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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

16 authors.

Xuan Zou *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Xuan Lin *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
He Cheng *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yusheng Chen *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Ruijie WangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Mingjian MaDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yu LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Zhengjie DaiDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yesboli TasihengDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yu YanDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Qinqin HouDepartment of Pathology Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Fei DingDepartment of Pathology Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Huan ChenDepartment of Pathology Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xianjun YuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China liuchen@fudanpci.org wangxu2013@fudan.edu.cn yuxianjun@fudanpci.org.ORCID 0000-0002-6697-7143
Xu WangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China liuchen@fudanpci.org wangxu2013@fudan.edu.cn yuxianjun@fudanpci.org.ORCID 0000-0001-6920-0375
Chen LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China liuchen@fudanpci.org wangxu2013@fudan.edu.cn yuxianjun@fudanpci.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor-associated tertiary lymphoid structures (TLSs) are functional immune-responsive niches that are not fully understood in pancreatic ductal adenocarcinoma (PDAC).

methodsFluorescent multiplex immunohistochemistry was performed on sequential sections of surgically resected tumor tissues from 380 PDAC patients without preoperative treatment (surgery alone (SA)) and 136 patients pretreated with neoadjuvant treatment (NAT). Multispectral images were processed via machine learning and image processing platforms, inForm V.2.4 and HALO V.3.2; TLS regions were segmented, and the cells were identified and quantified. The cellular composition and immunological properties of TLSs and their adjacent tissues in PDAC were scored and compared, and their association with prognosis was further examined.

resultsIntratumoral TLSs were identified in 21.1% (80/380) of patients in the SA group and 15.4% (21/136) of patients in the NAT group. In the SA group, the presence of intratumoral TLSs was significantly associated with improved overall survival (OS) and progression-free survival. The existence of intratumoral TLSs was correlated with elevated levels of infiltrating CD8+T, CD4+T, B cells and activated immune cells in adjacent tissues. A nomogram model was generated with TLS presence as a variable, which successfully predicted PDAC patient OS in an external validation cohort (n=123). In the NAT group, samples exhibited a lower proportion of B cells and a higher proportion of regulatory T cells within intratumoral TLSs. Additionally, these TLSs were smaller in size, with a lower overall maturation level and reduced immune cell activation, and the prognostic value of TLS presence was insignificant in the NAT cohort.

conclusionOur study systematically revealed the cellular properties and prognostic values of intratumoral TLSs in PDAC and described the potential impact of NAT on TLS development and function.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsTertiary Lymphoid StructuresHumansPrognosisGastrointestinal NeoplasmsTumor BiomarkersTumor Microenvironment

Identifiers

PMID37364934
PMCPMC10410893

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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.