Evidence map›Paper›PMID 42208980›Full record

ArticleJournal for immunotherapy of cancer2026

Pretreatment intratumoral mature TLSs in non-clear cell renal cell carcinoma are associated with response to immunotherapy rechallenge.

Yanfeng Tang, Junru Chen, Jue Hu, Dingbang Liu, Keha Ma, Yuntian Chen, Ling Wang, Xingming Zhang, Xu Hu, Jinge Zhao and 17 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

27 authors.

Yanfeng TangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.ORCID http://orcid.org/0009-0008-3369-5917
Junru ChenDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.ORCID http://orcid.org/0000-0003-4553-6979
Jue HuDepartment of Pathology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.ORCID http://orcid.org/0000-0003-3221-5957
Dingbang LiuDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.ORCID http://orcid.org/0000-0002-4304-0032
Keha MaDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Yuntian ChenDepartment of Radiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Ling WangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Xingming ZhangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Xu HuDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Jinge ZhaoDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Xi WangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Jingjing GuoDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Haoyang LiuDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Junjie ZhaoDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Zilin WangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Nanwei XuDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Sike HeDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Xinyuan WeiDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Yuan WangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Zeqi WangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Jin YaoDepartment of Radiology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Ni ChenDepartment of Pathology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Pengfei ShenDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Zhenhua LiuDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Guangxi SunDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China drliangjiayu@163.com kucaizeng@163.com sungx077@126.com.ORCID http://orcid.org/0000-0003-3719-2643
Hao ZengDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China drliangjiayu@163.com kucaizeng@163.com sungx077@126.com.ORCID http://orcid.org/0000-0003-0818-8151
Jiayu LiangDepartment of Urology, West China Hospital of Sichuan University, Chengdu, Sichuan, China drliangjiayu@163.com kucaizeng@163.com sungx077@126.com.ORCID http://orcid.org/0000-0002-5126-4511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile immune checkpoint inhibitor (ICI)-based therapy has shown promising efficacy in patients with metastatic non-clear cell renal cell carcinoma (nccRCC) in the first-line setting, the optimal treatment following disease progression remains undefined. We aimed to investigate the efficacy, safety, and predictive markers of ICI rechallenge in this population.

methods39 patients with metastatic nccRCC who received ICI rechallenge were enrolled. Key outcomes included objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival. Whole exome sequencing, bulk RNA sequencing, and multiplex immunofluorescence (mIF) were performed to further explore potential biomarkers associated with the efficacy of ICI-rechallenge among nccRCC.

resultsFollowing ICI-rechallenge, the cohort demonstrated a median PFS of 11.8 months, an ORR of 13.9% and a DCR of 69.4%. Among clinicopathological variables, the fumarate hydratase-deficient renal cell carcinoma subtype was the only factor associated with the potential clinical benefit from ICI-rechallenge. Transcriptomic analysis revealed that an enrichment of B cells and central memory T cell signatures was associated with longer PFS (21.3 vs 7.9 months). Notably, patients with a higher mature intratumoral tertiary lymphoid structure (m-iTLS) score assessed by mIF showed higher ORR (50.0% vs 0.0%) and longer PFS (28.2 vs 5.0 months) compared with those with a lower m-iTLS score. In terms of safety, ICI rechallenge was generally well tolerated, with no accumulation or treatment-related deaths observed.

conclusionsICI rechallenge may offer favorable clinical benefit and acceptable safety in patients with metastatic nccRCC. Higher density of mature iTLSs correlated with the efficacy of ICI-rechallenge but warrants further validation.

Indexed as

Carcinoma, Renal CellImmune Checkpoint InhibitorsImmunotherapyKidney NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedTumor MicroenvironmentImmune Checkpoint InhibitorsImmune Checkpoint InhibitorKidney CancerTumor microenvironment - TME

Identifiers

PMID42208980
PMCPMC13223679

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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.