Evidence map›Paper›PMID 37985152›Full record

ArticleZhongguo fei ai za zhi = Chinese journal of lung cancer2023

[Evaluation of Efficacy and Prognosis Analysis of Stage III-IV SMARCA4-deficient 
Non-small Cell Lung Cancer Treated by PD-1 Immune Checkpoint Inhibitors plus 
Chemotherapy and Chemotherapy].

Xinjuan Wang, Meng Tu, Hongxia Jia, Hongping Liu, Yan Wang, Yibo Wang, Nan Jiang, Chunya Lu, Guojun Zhang

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Translational lung cancer research · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. [Research Progress on SMARCA4 Mutation Non-small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2024
    Review
  8. 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

9 authors at 1 institution in 1 country.

Xinjuan WangDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Meng TuDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Hongxia JiaDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Hongping LiuDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Yan WangDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Yibo WangDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Nan JiangDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Chunya LuDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
Guojun ZhangDepartment of Pulmonary Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe SMARCA4 mutation has been shown to account for at least 10% of non-small cell lung cancer (NSCLC). In the present, conventional radiotherapy and targeted therapy are difficult to improve outcomes due to the highly aggressive and refractory nature of SMARCA4-deficient NSCLC (SMARCA4-DNSCLC) and the absence of sensitive site mutations for targeted drug therapy, and chemotherapy combined with or without immunotherapy is the main treatment. Effective SMARCA4-DNSCLC therapeutic options, however, are still debatable. Our study aimed to investigate the efficacy and prognosis of programmed cell death 1 (PD-1) immune checkpoint inhibitors (ICIs) in combination with chemotherapy and chemotherapy in patients with stage III-IV SMARCA4-DNSCLC.

methods46 patients with stage III-IV SMARCA4-DNSCLC were divided into two groups based on their treatment regimen: the chemotherapy group and the PD-1 ICIs plus chemotherapy group, and their clinical data were retrospectively analyzed. Efficacy assessment and survival analysis were performed in both groups, and the influencing factors for prognosis were explored for patients with SMARCA4-DNSCLC.

resultsMale smokers are more likely to develop SMARCA4-DNSCLC. There was no significant difference in the objective response rate (76.5% vs 69.0%, P=0.836) between chemotherapy and the PD-1 ICIs plus chemotherapy or the disease control rate (100.0% vs 89.7%, P=0.286). The one-year overall survival rate in the group with PD-1 ICIs plus chemotherapy was 62.7%, and that of the chemotherapy group was 46.0%. The difference in median progression-free survival (PFS) between the PD-1 ICIs plus chemotherapy group and the chemotherapy group was statistically significant (9.3 mon vs 6.1 mon, P=0.048). The results of Cox regression analysis showed that treatment regimen and smoking history were independent influencing factors of PFS in patients with stage III-IV SMARCA4-DNSCLC, and family history was an individual influencing factor of overall survival in patients with stage III-IV SMARCA4-DNSCLC.

conclusionsTreatment regimen may be a prognostic factor for patients with SMARCA4-DNSCLC, and patients with PD-1 ICIs plus chemotherapy may have a better prognosis.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsDNA HelicasesHumansImmune Checkpoint InhibitorsMaleNuclear ProteinsPrognosisProgrammed Cell Death 1 ReceptorRetrospective StudiesTranscription FactorsAntineoplastic Agents, ImmunologicalDNA HelicasesImmune Checkpoint InhibitorsNuclear ProteinsProgrammed Cell Death 1 ReceptorSMARCA4 protein, humanTranscription FactorsChemotherapyCox proportional hazards modelsImmune checkpoint inhibitorsLung neoplasmsPrognosisSMARCA4

Identifiers

PMID37985152
PMCPMC10600746
OpenAlexW4388869757

What OpenQuestion holds

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Registered trials

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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.