Evidence map›Paper›PMID 38052215›Full record

ArticleCell reports. Medicine2023

Tumor-immune microenvironment and NRF2 associate with clinical efficacy of PD-1 blockade combined with chemotherapy in lung squamous cell carcinoma.

Jianchun Duan, Yun Zhang, Ran Chen, Liang Liang, Yi Huo, Shun Lu, Jun Zhao, Chunhong Hu, Yuping Sun, Kunyu Yang and 12 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03594747 (A Phase 3, Multicenter, Randomized Open-Label Study to Compare the Efficacy and Safety of Tislelizumab), which is not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.2field-weighted citation impact, top 3% 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.

NCT03594747 phase3completednot on this map

A Phase 3, Multicenter, Randomized Open-Label Study to Compare the Efficacy and Safety of Tislelizumab (BGB A317, Anti-PD1 Antibody) Combined With Paclitaxel Plus Carboplatin or Nab Paclitaxel Plus Carboplatin Versus Paclitaxel Plus Carboplatin Alone as First-Line Treatment for Untreated Advanced Squamous Non-small Cell Lung Cancer

TypeinterventionalSponsorBeiGeneRan2018 to 2023Enrolled360ConditionsNon-Small Cell Lung CancerArmsTislelizumab, Paclitaxel, Nab-paclitaxel, Carboplatin
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 27 citations in OpenAlex.

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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

22 authors at 12 institutions in 2 countries.

Jianchun DuanState Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Yun ZhangBeiGene (Beijing) Co., Ltd., Beijing 100022, China.
Ran ChenCenter for Clinical Research and Translational Medicine, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China; Department of General Surgery, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China.
Liang LiangBeiGene (Beijing) Co., Ltd., Beijing 100022, China.
Yi HuoBeiGene (Beijing) Co., Ltd., Beijing 100022, China.
Shun LuShanghai Lung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai 200025, China.
Jun ZhaoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Department of Thoracic Medical Oncology, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Chunhong HuOncology Department, The Second Hospital of Central South University, Changsha 410011, China.
Yuping SunOncology Department, Jinan Central Hospital, Shandong 250013, China.
Kunyu YangUnion Hospital, Cancer Center, Tongji Medical College, Huazhong University of Science and Technology, Hubei 430074, China.
Mingwei ChenDepartment of Respiratory Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China.
Yan YuDepartment of Respiratory Medicine, Harbin Medical University Cancer Hospital, Harbin 150081, China.
Jianming YingDepartment of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Ruiqi HuangBeiGene (Shanghai) Co., Ltd., Shanghai 200040, China.
Xiaopeng MaBeiGene (Beijing) Co., Ltd., Beijing 100022, China.
Shiangjiin LeawBeiGene (Shanghai) Co., Ltd., Shanghai 200040, China.
Fan BaiBeiGene (Shanghai) Co., Ltd., Shanghai 200040, China.
Zhirong ShenBeiGene (Beijing) Co., Ltd., Beijing 100022, China.
Shangli CaiBurning Rock Biotech, Guangzhou 510300, China.
Daming GaoState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, China; University of the Chinese Academy of Sciences, 19A Yuquan Road, Beijing 100049, China; School of Life Science, Hangzhou Institute for Advanced Study, University of the Chinese Academy of Sciences, Hangzhou 310024, China.
Jie WangState Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China. Electronic address: zlhuxi@163.com.
Zhijie WangState Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China. Electronic address: jie_969@163.com.
BeiGene (China) · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNBurning Rock Biotech (China) · CNCentral South University · CNChinese Academy of Sciences · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CNHarbin Medical University · CNJinan Central Hospital · CNPeking University · CNShanghai Jiao Tong University · CNTongji University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RATIONALE-307 study (ClinicalTrials.gov: NCT03594747) demonstrates prolonged progression-free survival (PFS) with first-line tislelizumab plus chemotherapy versus chemotherapy in advanced lung squamous cell carcinoma (LUSC; N = 360). Here we describe an immune-related gene expression signature (GES), composed of genes involved in both innate and adaptive immunity, that appears to differentiate tislelizumab plus chemotherapy PFS benefit versus chemotherapy. In contrast, a tislelizumab plus chemotherapy PFS benefit is observed regardless of programmed death ligand 1 (PD-L1) expression or tumor mutational burden (TMB). Genetic analysis reveals that NRF2 pathway activation is enriched in PD-L1

Indexed as

Carcinoma, Non-Small-Cell LungCarcinoma, Squamous CellLung NeoplasmsB7-H1 AntigenBiomarkers, TumorHumansLungMutationNF-E2-Related Factor 2Programmed Cell Death 1 ReceptorTreatment OutcomeTumor MicroenvironmentB7-H1 AntigenBiomarkers, TumorNFE2L2 protein, humanNF-E2-Related Factor 2Programmed Cell Death 1 Receptorbiomarkersclinical trialgene expression signatureimmunotheraphyNRF2PD-1 blockadePD-L1squamous NSCLCtislelizumabtumor mutational burden

Identifiers

PMID38052215
PMCPMC10772345
OpenAlexW4389305264

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.