Evidence map›Paper›PMID 39543276›Full record

ArticleNPJ precision oncology2024

Tertiary lymphoid structures potentially promote immune checkpoint inhibitor response in SMARCB1-deficient medullary renal cell carcinoma.

Yanfeng Tang, Junru Chen, Mengxin Zhang, Xu Hu, Jingjing Guo, Yaowen Zhang, Yuntian Chen, Haoyang Liu, Junjie Zhao, Ni Chen and 2 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Molecularly defined renal cell carcinomas.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2026
    Review
  3. Review
  4. Review
  5. Article
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

12 authors.

Yanfeng Tang *Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Junru Chen *Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Mengxin Zhang *Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
Xu HuDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Jingjing GuoDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Yaowen ZhangDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID http://orcid.org/0000-0003-4411-1215
Yuntian ChenDepartment of Radiology, West China Hospital, Sichuan University, Chengdu, China.
Haoyang LiuDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Junjie ZhaoDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Ni ChenDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China. chenni1@163.com.
Guangxi SunDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. sungx077@126.com.ORCID http://orcid.org/0000-0003-3719-2643
Hao ZengDepartment of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. kucaizeng@163.com.ORCID http://orcid.org/0000-0002-1267-0509

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82373422
6 · The paper itself

Abstract

The WHO's classification of renal cell carcinoma (RCC) has identified loss of SMARCB1 as one of the driven mutations. Despite intensive postoperative interventions, the prognosis for SMARCB1-deficient medullary RCC remains poor, indicating insufficiency in current therapy. Herein, we reported the treatment outcomes of five patients with metastatic SMARCB1-deficient medullary RCC and molecular correlates. Four patients were treated with first-line immune checkpoint inhibitors (ICI) plus tyrosine kinase inhibitors (TKI) combination therapy with a median PFS (mPFS) of 12.3 months. Transcriptomic analysis revealed enrichment of immune-related pathways in SMARCB1-deficient medullary RCC compared to clear-cell and papillary RCC. Multiple immunofluorescence (mIF) revealed the association between the formation of mature tertiary lymphoid structures (TLSs) and the favorable response to ICI-based combination therapy. In conclusion, ICI-based combination therapy showed promising anti-tumor activity in SMARCB1-deficient medullary RCC patients. The presence of mature tertiary TLSs may partially elucidate the mechanism underlying treatment response.

Identifiers

PMID39543276
PMCPMC11564649

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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.