Evidence map›Paper›PMID 34512623›Full record

ArticleFrontiers in immunology2021

Guangsheng Zhu, Ruifeng Shi, Yongwen Li, Zihe Zhang, Songlin Xu, Chen Chen, Peijun Cao, Hongbing Zhang, Minghui Liu, Zhenhua Pan and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
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

35 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Review
  3. Myoepithelial tumor withFrontiers in oncology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Targeting WEE1 to Overcome ARID1A Mutation-Driven Osimertinib Resistance in EGFR-Mutant Lung Cancer.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Article
  8. Article
  9. Review
  10. [ARID1B Gene Deletion Promotes the Proliferation, Migration and Invasion 
of NSCLC Cells].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Therapeutic Role of Synthetic Lethality inJournal of immunotherapy and precision oncology · 2024
    Review
  20. 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

12 authors at 1 institution in 2 countries.

Guangsheng ZhuDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Ruifeng ShiDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Yongwen LiTianjin Lung Cancer Institute, Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Medical University General Hospital, Tianjin, China.
Zihe ZhangDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Songlin XuDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Chen ChenTianjin Lung Cancer Institute, Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Medical University General Hospital, Tianjin, China.
Peijun CaoDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Hongbing ZhangDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Minghui LiuDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Zhenhua PanTianjin Lung Cancer Institute, Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Medical University General Hospital, Tianjin, China.
Hongyu LiuTianjin Lung Cancer Institute, Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Medical University General Hospital, Tianjin, China.
Jun ChenDepartment of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Tianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Worldwide, non-small cell lung cancer (NSCLC) has the highest morbidity and mortality of all malignancies. The lack of responsiveness to checkpoint inhibitors is a central problem in the modern era of cancer immunotherapy, with the rapid development of immune checkpoint inhibitors (ICIs) in recent years. The human switch/sucrose nonfermentable (SWI/SNF) chromatin-remodeling complex has been reported to be recurrently mutated in patients with cancer, and those with SWI/SNF mutations have been reported to be sensitive to ICIs. Six reported cohorts, a total of 3416 patients, were used to analyze the mutation status of ARID1A, ARID1B, ARID2 and SMARCA4 in patients with NSCLC and the effect of mutations on prognosis after ICIs. Finally, a nomogram was established to guide the clinical use of ICIs. The results show that patients with NSCLC who have ARID1A, ARID1B, and ARID2 mutations of the SWI/SNF complex were more likely to benefit from ICI therapy.

Indexed as

MutationBiomarkers, TumorCarcinoma, Non-Small-Cell LungClinical Decision-MakingDecision Support TechniquesDNA-Binding ProteinsDNA Mutational AnalysisFemaleHumansImmune Checkpoint InhibitorsLung NeoplasmsMaleMiddle AgedNomogramsPatient SelectionPredictive Value of TestsARID1A protein, humanARID1B protein, humanARID2 protein, humanBiomarkers, TumorDNA-Binding ProteinsImmune Checkpoint InhibitorsTranscription Factorsanti-PD1/PD-L1immunotherapynon-small cell lung cancerPD-1/PD-L1 inhibitorsSWI/SNF complex

Identifiers

PMID34512623
PMCPMC8426508
OpenAlexW3198065124

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.