# Radiomic subtypes predict survival and chemotherapy benefit in stage I lung adenocarcinoma: a multicenter study

**Authors:** Guangyu Tao, Dongying Wang, Xin Cheng, Zhenghai Lu, Hua Zhong, Hong Yu, Wei Nie

PMC · DOI: 10.1186/s13244-026-02228-1 · Insights into Imaging · 2026-03-02

## TL;DR

This study uses CT scans to identify radiomic subtypes in stage I lung cancer patients, which predict survival and chemotherapy benefits.

## Contribution

A CT-based radiomic subtype system is developed to predict survival and chemotherapy benefit in stage I lung adenocarcinoma.

## Key findings

- Three radiomic subtypes with significant differences in overall survival were identified.
- The high-risk subtype showed a strong association with poor survival and inflammatory imbalance.
- Stage IB patients in the high-risk subtype benefited significantly from adjuvant chemotherapy.

## Abstract

Postoperative survival outcomes vary substantially among patients diagnosed with stage I lung adenocarcinoma (LUAD). This study aimed to develop CT-based radiomic subtypes using unsupervised clustering to assess their association with overall survival (OS), systemic nutritional-inflammatory status, and adjuvant chemotherapy benefit.

A total of 496 stage I LUAD patients from two independent centers were included. Preoperative CT radiomic features (n = 1218) were extracted, and subtypes were derived using the K-means clustering algorithm. The independent prognostic value of these subtypes, along with their capacity to predict the benefit of adjuvant chemotherapy, was evaluated through multivariable Cox regression and treatment-by-subtype interaction analyses.

Three radiomic subtypes with significant prognostic differences in OS were identified. The high-risk subtype, Cluster 2, exhibited distinct clinical characteristics and was associated with markedly poorer OS (hazard ratio [HR] = 15.71, p < 0.001, compared to Cluster 0). Cluster 2 also showed an inflammatory imbalance, with elevated systemic immune-inflammation index and neutrophil-to-lymphocyte ratio, and  a decreased lymphocyte-to-monocyte ratio. Notably, a significant interaction was found between subtypes and adjuvant chemotherapy (interaction p < 0.001, Cluster 2 vs Cluster 0). Subgroup analysis indicated that stage IB patients within Cluster 2 derived a significant survival benefit from adjuvant chemotherapy (interaction p = 0.003 vs Cluster 0).

This study developed a CT-based radiomic subtype system using unsupervised clustering that identifies high-risk stage I LUAD patients with systemic inflammatory imbalance. Notably, these subtypes predict differential survival benefits from adjuvant chemotherapy in high-risk stage IB patients, thereby supporting personalized postoperative treatment strategies.

This CT-based radiomic subtype system stratifies prognosis and identifies stage I LUAD patients who may benefit from adjuvant chemotherapy, enabling personalized treatment decisions in radiology.

Conventional tumor-node-metastasis (TNM) staging does not adequately capture tumor heterogeneity in stage I LUAD.Three CT-based radiomic subtypes were established, with the high-risk subgroup correlating with systemic inflammatory imbalance and poorer OS.CT-based radiomic stratification identifies stage IB patients who benefit from adjuvant chemotherapy, supporting personalized postoperative management.

Conventional tumor-node-metastasis (TNM) staging does not adequately capture tumor heterogeneity in stage I LUAD.

Three CT-based radiomic subtypes were established, with the high-risk subgroup correlating with systemic inflammatory imbalance and poorer OS.

CT-based radiomic stratification identifies stage IB patients who benefit from adjuvant chemotherapy, supporting personalized postoperative management.

## Linked entities

- **Diseases:** lung adenocarcinoma (MONDO:0005061)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, STK11 (serine/threonine kinase 11) [NCBI Gene 6794] {aka LKB1, PJS, hLKB1}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}
- **Diseases:** -metastasis (MESH:D009362), PNI (MESH:D044342), death (MESH:D003643), immune (MESH:D007154), stage IB disease (MESH:D007676), cytotoxic (MESH:D064420), TNM (MESH:D008207), ARI (MESH:D000275), CT (MESH:C000719218), LVI (MESH:D009361), NLR (MESH:D015467), Inflammation (MESH:D007249), lymphocyte dysfunction (MESH:D015451), Tumor (MESH:D009369), MIA (MESH:D000230), VPI (MESH:D010995), Lung Cancer (MESH:D008175), IB disease (MESH:C562594), I LUAD (MESH:D000077192), I (MESH:D006969), AIS (MESH:D065311)
- **Chemicals:** cisplatin (MESH:D002945), pemetrexed (MESH:D000068437), carboplatin (MESH:D016190), gemcitabine (MESH:D000093542), platinum (MESH:D010984), paclitaxel (MESH:D017239), vinorelbine (MESH:D000077235)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12953834