Evidence map›Paper›PMID 42811057›Full record

ArticleNature communications2026

Clinical attribute-based risk matrix for prognostication in immunotherapy-treated non-small cell lung cancer.

Lu Wang, Nan Xu, Hairui Wang, Bosinan Chen, Qiuju Sheng, Jie Zhang, Zhaoshuo Liu, Taixue An, Guanchao Ye, Jianing Sun and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lu Wang *School of Health Management, China Medical University, Shenyang, Liaoning, China.
Nan Xu *School of Health Management, China Medical University, Shenyang, Liaoning, China.
Hairui Wang *Department of Radiology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Bosinan Chen *The First Hospital of China Medical University, Shenyang, Liaoning, China.
Qiuju Sheng *Department of Infectious Diseases, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Jie Zhang *Department of Medical Imaging, Zhuhai People's Hospital (The Affiliated Hospital of Beijing Institute of Technology, Zhuhai Clinical Medical College of Jinan University), Zhuhai, Guangdong, China.
Zhaoshuo LiuSchool of Computer Science and Engineering, Northeastern University, Shenyang, China.
Taixue AnDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guanchao YeDepartment of Thoracic Surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jianing SunThe Second Clinical College, China Medical University, Shenyang, Liaoning, China.
Zhijian ZhangThe Fourth Clinical College, China Medical University, Shenyang, Liaoning, China.
Qiuyang HouDepartment of Radiology, The First Affiliated Hospital of University of Science and Technology of China (USTC), Division of Life Sciences and Medicine, USTC, Hefei, Anhui, China.
Bin LiuDepartment of Radiology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.
Song ChenDepartment of Nuclear Medicine, The First Hospital of China Medical University, Shenyang, Liaoning, China. chensongchina@163.com.ORCID 0000-0002-2639-6301
Li YuDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China. yulimail369@163.com.ORCID 0009-0001-9549-620X
Jiangdian SongSchool of Health Management, China Medical University, Shenyang, Liaoning, China. song.jd0910@gmail.com.ORCID 0000-0002-3355-9930

Funding

National Natural Science Foundation of China (National Science Foundation of China) 92259104
6 · The paper itself

Abstract

Biomarkers used to guide immunotherapy in non-small cell lung cancer (NSCLC) are invasive, variably available, and insufficient to capture clinical and regional heterogeneity, leaving many patients inadequately stratified for prognosis. We develop a clinical attribute-based framework that leverages routinely collected variables to estimate survival risk, even when baseline data are incomplete. We analyze 17 051 patients with NSCLC treated with immunotherapy, assembled from published cohorts and tertiary centers across multiple regions, and evaluate seventeen common clinical attributes using a two-stage survival modeling strategy with external validation in Western and East Asian populations. Clinical attributes exhibit context-dependent prognostic effects across variable-defined strata and survival endpoints, with performance status and disease stage emerging as the most consistent determinants of survival risk prediction, alongside region-specific modifiers. Here we show that this "start-anywhere" clinical risk matrix provides robust, population-aware prognostic stratification and complements biomarkers for assessing immunotherapy outcomes in patients with NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedPrognosisRisk AssessmentBiomarkers, Tumor

Identifiers

PMID42811057
PMCPMC13623942

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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.