Evidence map›Paper›PMID 41387877›Full record

ArticleJournal of translational medicine2025

Tumor immune microenvironment score predicts efficacy of immune checkpoint inhibitors-based regimens in advanced non-small cell lung cancer.

Jiacheng Dai, Huan Yan, Yangqian Chen, Yuda Zhang, Zhe Huang, Zhaohui Ruan, Fang Tian, Haoyue Qin, Qinqin Xu, Jin Wang and 6 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Jiacheng Dai *Early Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Huan Yan *Early Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Yangqian ChenDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Yuda ZhangDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Zhe HuangEarly Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Zhaohui RuanEarly Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Fang TianEarly Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Haoyue QinDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Qinqin XuSchool of Clinical Medicine, Qinghai University, Xining, Qinghai, 810000, China.
Jin WangDepartment of Translational Medicine, Amoy Diagnostics, Xiamen, Fujian, 361000, China.
Xing LiDepartment of Translational Medicine, Amoy Diagnostics, Xiamen, Fujian, 361000, China.
Peng ChengDepartment of Translational Medicine, Amoy Diagnostics, Xiamen, Fujian, 361000, China.
Changbin ZhuDepartment of Translational Medicine, Amoy Diagnostics, Xiamen, Fujian, 361000, China.
Nong YangDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Liang ZengEarly Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China.
Yongchang ZhangEarly Clinical Trial Center, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, 410013, China. zhangyongchang@csu.edu.cn.ORCID 0000-0002-6829-7176

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitor (ICI)-based regimens have become the standard first-line treatment for advanced non-small cell lung cancer (NSCLC). However, response rates vary widely, emphasizing the need for a predictive model to optimize patient selection and improve treatment outcomes.

methodsWe retrospectively analyzed 96 treatment-naïve patients with advanced NSCLC who received first-line ICI-based regimens (anti-PD-1 ± platinum chemotherapy) at Hunan Cancer Hospital. Pre-treatment tumor biopsies underwent bulk RNA sequencing to identify differentially expressed genes associated with progression-free survival (PFS). A five-gene Cox proportional hazards model, the Prediction model of Immunotherapy Efficacy (PIE), was developed and validated in two independent cohorts: ORIENT-11 (n = 113; chemo-ICI) and OAK (n = 344; ICI monotherapy). Multiplex immunofluorescence staining (CD8, CD56, CD16, Pan-CK, PD-L1, MAGEA2) was performed to validate immune-cell infiltration patterns and candidate biomarkers across PIE-defined risk groups.

resultsPatients in the long-survival group exhibited enrichment of IL7R

conclusionPIE represents a clinically relevant, transcriptome-based predictive model for evaluating the benefit of ICI treatment in advanced NSCLC. With further prospective validation, PIE may facilitate personalized patient selection and guide the development of novel strategies to overcome primary resistance.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung NeoplasmsTumor MicroenvironmentAgedBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedProportional Hazards ModelsReproducibility of ResultsRetrospective StudiesTreatment OutcomeBiomarkers, TumorImmune Checkpoint InhibitorsImmune checkpoint inhibitorNSCLCPFSPrognostic prediction

Identifiers

PMID41387877
PMCPMC12699922

What OpenQuestion holds

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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.