Evidence map›Paper›PMID 42709716›Full record

ArticlePLOS digital health2026

Topologically distinct intratumoral heterogeneity scores for predicting high-risk pathological grades in invasive lung adenocarcinoma: A multicenter study across four institutions.

Shanyue Lin, Yudian Mao, Qian He, Wanyin Qi, Sanhong Zhang, Wei Li, Zhichao Zuo

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shanyue LinDepartment of Radiology, Xiangtan Central Hospital(The Affiliated Hospital of Hunan University), Xiangtan, Hunan, China.ORCID https://orcid.org/0000-0002-5608-9978
Yudian MaoDepartment of Radiology, Xiangtan Central Hospital(The Affiliated Hospital of Hunan University), Xiangtan, Hunan, China.
Qian HeDepartment of Radiology, Xiangtan Central Hospital(The Affiliated Hospital of Hunan University), Xiangtan, Hunan, China.
Wanyin QiDepartment of Radiology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Sanhong ZhangDepartment of Radiology, Liuyang Hospital of Traditional Chinese Medicine, Changsha, Hunan, China.
Wei LiDepartment of Radiology, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.ORCID https://orcid.org/0000-0002-7267-6494
Zhichao ZuoDepartment of Radiology, Xiangtan Central Hospital(The Affiliated Hospital of Hunan University), Xiangtan, Hunan, China.ORCID https://orcid.org/0009-0004-4824-6138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-risk subtypes of invasive lung adenocarcinoma (IAC), particularly micropapillary- or solid-predominant patterns, are closely associated with poor prognosis. This multicenter retrospective study developed and validated a predictive model for the preoperative identification of these high-risk subtypes using topologically distinct intratumoral heterogeneity (ITH) scores derived from CT images. The study included 1,051 patients with IAC. Two complementary ITH scores were developed: a two-dimensional ITH score, which integrated local radiomics features with global pixel distribution patterns on the largest cross-sectional CT slice, and a three-dimensional ITH score, which extended this quantification across the entire tumor volume. Clinicoradiological features and ITH scores were incorporated as model inputs to construct six base machine learning classifiers and a final stacking ensemble classifier. Model interpretability and robustness were evaluated using SHapley Additive exPlanations (SHAP)-based ablation analyses. An independent dataset from The Cancer Imaging Archive (TCIA) was used for external validation to investigate associations between ITH scores and pathological characteristics, genomic features, recurrence-free survival, and overall survival. The stacking ensemble classifier achieved the best predictive performance, with an area under the receiver operating characteristic curve of 0.875, outperforming models based solely on radiomics features (0.834) or clinicoradiological features (0.792). SHAP analysis identified the 3D ITH score as the most influential contributor to model output, and TCIA validation showed that higher 3D ITH scores were associated with more aggressive tumor biology and poorer survival outcomes. The topologically distinct 3D ITH score may provide a clinically meaningful imaging biomarker for preoperative risk stratification in IAC.

Identifiers

PMID42709716
PMCPMC13552742

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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.