Analysis of the Correlation and Prognostic Significance of Tertiary Lymphoid Structures in Breast Cancer: A Radiomics‐Clinical Integration Approach

Author:

Li Kezhen123ORCID,Ji Juan4,Li Simin123,Yang Man135,Che Yurou135,Xu Zhu123,Zhang Yiyao135,Wang Mei135,Fang Zengyi135,Luo Liping135,Wu Chuan15,Lai Xin15,Dong Juan26,Zhang Xinlan7,Zhao Na4,Liu Yang4,Wang Weidong1235

Affiliation:

1. Department of Radiation Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center Affiliated Cancer Hospital of University of Electronic Science and Technology of China Chengdu China

2. Department of Oncology, School of Clinical Medicine Southwest Medical University Luzhou China

3. Radiation Oncology Key Laboratory of Sichuan Province Chengdu China

4. Department of Pathology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center Affiliated Cancer Hospital of University of Electronic Science and Technology of China Chengdu China

5. Sichuan Cancer Hospital and Institute, School of Medicine University of Electronic Science and Technology of China Chengdu China

6. Department of Chest Meishan Cancer Hospital Meishan China

7. Department of Breast Surgery Chengdu Women's and Children's Hospital Chengdu China

Abstract

BackgroundTertiary lymphoid structures (TLSs) are potential prognostic indicators. Radiomics may help reduce unnecessary invasive operations.PurposeTo analyze the association between TLSs and prognosis, and to establish a nomogram model to evaluate the expression of TLSs in breast cancer (BC) patients.Study TypeRetrospective.PopulationTwo hundred forty‐two patients with localized primary BC (confirmed by surgery) were divided into BC + TLS group (N = 122) and BC − TLS group (N = 120).Field Strength/Sequence3.0T; Caipirinha‐Dixon‐TWIST‐volume interpolated breath‐hold sequence for dynamic contrast‐enhanced (DCE) MRI and inversion‐recovery turbo spin echo sequence for T2‐weighted imaging (T2WI).AssessmentThree models for differentiating BC + TLS and BC − TLS were developed: 1) a clinical model, 2) a radiomics signature model, and 3) a combined clinical and radiomics (nomogram) model. The overall survival (OS), distant metastasis‐free survival (DMFS), and disease‐free survival (DFS) were compared to evaluate the prognostic value of TLSs.Statistical TestsLASSO algorithm and ANOVA were used to select highly correlated features. Clinical relevant variables were identified by multivariable logistic regression. Model performance was evaluated by the area under the receiver operating characteristic (ROC) curve (AUC), and through decision curve analysis (DCA). The Kaplan–Meier method was used to calculate the survival rate.ResultsThe radiomics signature model (training: AUC 0.766; test: AUC 0.749) and the nomogram model (training: AUC 0.820; test: AUC 0.749) showed better validation performance than the clinical model. DCA showed that the nomogram model had a higher net benefit than the other models. The median follow‐up time was 52 months. While there was no significant difference in 3‐year OS (P = 0.22) between BC + TLS and BC − TLS patients, there were significant differences in 3‐year DFS and 3‐year DMFS between the two groups.Data ConclusionThe nomogram model performs well in distinguishing the presence or absence of TLS. BC + TLS patients had higher long‐term disease control rates and better prognoses than those without TLS.Evidence Level2Technical EfficacyStage 2

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

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