Standardized 18F-FDG PET/CT radiomic features provide information on PD-L1 expression status in treatment-naïve patients with non-small cell lung cancer

Author:

Zhang Ruiyun123,Hohenforst-Schmidt Wolfgang4,Steppert Claus5,Sziklavari Zsolt6,Schmidkonz Christian7,Atzinger Armin7,Kuwert Torsten7,Klink Thorsten8910,Sterlacci William12,Hartmann Arndt1,Vieth Michael912,Förster Stefan1193

Affiliation:

1. Institute of Pathology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany

2. Pathology, Klinikum Bayreuth GmbH, Bayreuth, Germany

3. Nuclear Medicine, Klinikum Bayreuth GmbH, Bayreuth, Germany

4. Pneumology, Sana Klinikum Hof GmbH, Hof, Germany

5. Pneumology, Klinikum Coburg GmbH, Coburg, Germany

6. Thoracic Surgery, Klinikum Coburg GmbH, Coburg, Germany

7. Nuclear Medicine, Universitätsklinikum Erlangen, Erlangen, Germany

8. Radiology, Universitätsklinikum Würzburg, Wurzburg, Germany

9. Medizincampus Oberfranken, Universitätsklinikum Erlangen, Bayreuth, Germany

10. Radiology, Klinikum Bayreuth GmbH, Bayreuth, Germany

11. Nuclear Medicine, Klinikum rechts der Isar der Technischen Universität München, Munchen, Germany

Abstract

Abstract Purpose To study the relationship between standardized 18F-FDG PET/CT radiomic features and clinicopathological variables and programmed death ligand-1 (PD-L1) expression status in non-small cell lung cancer (NSCLC) patients. Methods 58 NSCLC patients with preoperative 18F-FDG PET/CT scans and postoperative results of PD-L1 expression were retrospectively analysed. A standardized, open-source software was used to extract 86 radiomic features from PET and low-dose CT images. Univariate analysis and multivariate logistic regression were used to find independent predictors of PD-L1 expression. The Area Under the Curve (AUC) of receiver operating characteristic (ROC) curve was used to compare the ability of variables and their combination in predicting PD-L1 expression. Results Multivariate logistic regression resulted in the PET radiomic feature GLRLM_LGRE (Odds Rate (OR): 0.300 vs 0.114, 95% confidence interval (CI): 0.096–0.931 vs 0.021–0.616, in NSCLC and adenocarcinoma respectively) and the CT radiomic feature GLZLM_SZE (OR: 3.338 vs 7.504, 95%CI: 1.074–10.375 vs 1.382–40.755, in NSCLC and adenocarcinoma respectively), being independent predictors of PD-L1 status. In NSCLC group, after adjusting for gender and histology, the PET radiomic feature GLRLM_LGRE (OR: 0.282, 95%CI: 0.085–0.936) remained an independent predictor for PD-L1 status. In the adenocarcinoma group, when adjusting for gender the PET radiomic feature GLRLM_LGRE (OR: 0.115, 95%CI: 0.021–0.631) and the CT radiomic feature GLZLM_SZE (OR: 7.343, 95%CI: 1.285–41.965) remained associated with PD-L1 expression. Conclusion NSCLC and adenocarcinoma with PD-L1 expression show higher tumour heterogeneity. Heterogeneity-related 18F-FDG PET and CT radiomic features showed good ability to non-invasively predict PD-L1 expression.

Publisher

Georg Thieme Verlag KG

Subject

Radiology, Nuclear Medicine and imaging,General Medicine

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