Research Article
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Year 2025, , 164 - 173, 01.01.2025
https://doi.org/10.31067/acusaglik.1549756

Abstract

References

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  • 5. Liu X, Guo CY, Tou FF, et al. Association of PD-L1 expression status with the efficacy of PD-1/PD-L1 inhibitors and overall survival in solid tumours: a systematic review and meta-analysis. Int J Cancer. 2020;147:116-27.
  • 6. Grant MJ, Herbst RS and Goldberg SB. Selecting the optimal immunotherapy regimen in drivernegative metastatic NSCLC. Nat Rev Clin Oncol 2021;18: 625-44.
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  • 15. Sezer A, Kilickap S, Gümüş M, et al Cemiplimab monotherapy for first-line treatment of advanced non-small-cell lung cancer with PD-L1 of at least 50%: a multicentre, open-label, global, phase 3, randomised, controlled trial. Lancet. 2021;397:592-604. LANCET.
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  • 22. Hu B, Chen W, Zhang Y, et al. 18F-FDG maximum standard uptake value predicts PD-L1 expression on tumor cells or tumor infiltrating immune cells in non-small cell lung cancer. Ann Nucl Med 2020;34:322-8.
  • 23. Hu B, Xiao J, Xiu Y, et al. Correlation of PD-L1 expression on tumor cell and tumor infiltrating immune cell with 18F-fluorodeoxyglucose uptake on PET/computed tomography in surgically resected pulmonary adenocarcinoma. Nucl Med Commun 2020; 41:252–9.
  • 24. Monaco L, De Bernardi E, Bono F, et al. The "digital biopsy" in non-small cell lung cancer (NSCLC): a pilot study to predict the PD-L1 status from radiomics features of [18F]FDG PET/CT. Eur J Nucl Med Mol Imaging. 2022;49:3401-11.
  • 25. Xu X, Li J, Yang Y, et al. The correlation between PD-L1 expression and metabolic parameters of 18FDG PET/CT and the prognostic value of PD-L1 in non-small cell lung cancer. Clin Imaging. 2022;89:120-7.
  • 26. Norikane T, Ishimura M, Mitamura K, et al. Texture Features of 18F-Fluorodeoxyglucose Positron Emission Tomography for Predicting Programmed Death-Ligand-1 Levels in Non-Small Cell Lung Cancer. J Clin Med. 2024;13:1625.
  • 27. Li J, Ge S, Sang S, et al. Evaluation of PD-L1 Expression Level in Patients With Non-Small Cell Lung Cancer by 18F-FDG PET/CT Radiomics and Clinicopathological Characteristics. Front Oncol. 2021;11:789014.
  • 28. Cui, Y., and X. Li. PD-L1 in Lung Adenocarcinoma: Insights into the Role of 18F-FDG PET/CT. Cancer Manag Res. 2020;12:6385-95.
  • 29. Wu X, Huang Y, Zhao Q, et al. PD-L1 expression correlation with metabolic parameters of FDG PET/CT and clinicopathological characteristics in non-small cell lung cancer. EJNMMI Res. 2020;10:51.
  • 30. Wang D, Li Y, Chen X, et al. Prognostic significance of volume-based 18F-FDG PET/CT parameters and correlation with PD-L1 expression in patients with surgically resected lung adenocarcinoma. Medicine (Baltimore). 2021;100:e27100.

Baseline 18F FDG PET/CT imaging in NSCLC: Possible utility in predicting strong-positive PD-L1 expression

Year 2025, , 164 - 173, 01.01.2025
https://doi.org/10.31067/acusaglik.1549756

Abstract

Background/Purpose: To assess whether 18F FDG PET/CT imaging can predict non-small cell lung cancer (NSCLC) patients with strong PD-L1 expression (≥50%).
Methods: This retrospective study analyzed 149 NSCLC patients who had undergone baseline 18F FDG PET/CT imaging from June 2021 to May 2024. We recorded age, sex, smoking history, histopathology, TNM stage, metastasis, and PD-L1 expression levels. PET/CT parameters such as SUVmax, SUVmean, metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were recorded. Patients were dichotomized based on two PD-L1 expression thresholds, as measured by immunohistochemistry: higher or lower than 1% (<1%, n = 62 versus >1%, n = 87) and higher or lower than 50% (<50%, n = 100 versus ≥50%, n = 39).
Results: No significant results were found for the comparison of PD-L1 negative (<1%) and positive (≥1%) patients. The <50% and ≥50% groups were similar in terms of all examined characteristics and PET/CT parameters except for TLG, which was significantly higher among patients with strong PD-L1 expression. ROC analysis revealed an area under curve of 0.606 (95% CI: 0.508–0.705, p = 0.049) for the discrimination of patients with and without strong PD-L1 expression, yielding 89.7% sensitivity, 30% specificity, and 45.6% overall accuracy.
Conclusion: This study identified TLG as a potential predictor for NSCLC patients with strong PD-L1 expression (≥50%) based on 18F FDG PET/CT imaging, despite low accuracy. High sensitivity and negative predictive value suggest a role as a supportive tool in screening.

Supporting Institution

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References

  • 1. Sung H, Ferlay J, Siegel RL, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71:209-49.
  • 2. Hellmann MD, Li BT, Chaft JE, et al. Chemotherapy remains an essential element of personalized care for persons with lung cancers. Ann Oncol. 2016;27:1829-35.
  • 3. Iwai Y, Ishida M, Tanaka Y, et al. Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade. Proc Natl Acad Sci USA 2002;99:12293–97.”
  • 4. Zhang J, Dang F, Ren J, et al. Biochemical aspects of PD-L1 regulation in cancer immunotherapy. Trends Biochem Sci. 2018;43:1014-32.
  • 5. Liu X, Guo CY, Tou FF, et al. Association of PD-L1 expression status with the efficacy of PD-1/PD-L1 inhibitors and overall survival in solid tumours: a systematic review and meta-analysis. Int J Cancer. 2020;147:116-27.
  • 6. Grant MJ, Herbst RS and Goldberg SB. Selecting the optimal immunotherapy regimen in drivernegative metastatic NSCLC. Nat Rev Clin Oncol 2021;18: 625-44.
  • 7. Sacher, AG, and L. Gandhi. Biomarkers for the clinical use of PD-1/PD-L1 inhibitors in non-small-cell lung cancer: a review. JAMA Oncol. 2016;2:1217–22.
  • 8. Genentech Inc. Administration USFaD. Tecentriq (Atezolizumab) [Package Insert], Full Prescribing Information. U.S. Food and Drug Administration; 2023.
  • 9. National Comprehensive Cancer Network (NCCN). NCCN Clinical Practice Guidelines in Oncology. Non-small Cell Lung Cancer version 4.2021, 2021.
  • 10. Bubendorf L, Lantuejoul S, de Langen AJ, et al. Nonsmall cell lung carcinoma: diagnostic difficulties in small biopsies and cytological specimens: Number 2 in the Series “Pathology for the clinician” Edited by Peter Dorfmüller and Alberto Cavazza. Eur Respir Rev. 2017;26:170007.
  • 11. Takada K, Toyokawa G, Okamoto T, et al. Metabolic characteristics of programmed cell death-ligand 1-expressing lung cancer on (18) Fluorodeoxyglucose positron emission tomography/computed tomography. Cancer Med. 2017;6:2552-61.
  • 12. Kaira K, Shimizu K, Kitahara S, et al. 2-Deoxy-2-[fluorine-18] fluoro-d-glucose uptake on positron emission tomography is associated with programmed death ligand-1 expression in patients with pulmonary adenocarcinoma. Eur J Cancer. 2018;101:181–90.
  • 13. Detterbeck FC, Boffa DJ, Kim AW, et al. The Eighth Edition Lung Cancer Stage Classiffication. Chest 2017; 51:193-203.
  • 14. Boellaard R, Delgado-Bolton R, Oyen WJ, et al. European Association of Nuclear Medicine (EANM). FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0. Eur J Nucl Med Mol Imaging 2015;42:328–54.
  • 15. Sezer A, Kilickap S, Gümüş M, et al Cemiplimab monotherapy for first-line treatment of advanced non-small-cell lung cancer with PD-L1 of at least 50%: a multicentre, open-label, global, phase 3, randomised, controlled trial. Lancet. 2021;397:592-604. LANCET.
  • 16. Borghaei H, Paz-Ares L, Horn L, et al. Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer. N Engl J Med. 2015;373:1627-39.
  • 17. Garon EB, Rizvi NA, Hui R, et al. Pembrolizumab for the treatment of non-small-cell lung cancer. N Engl J Med., 2015;372:2018-28.
  • 18. Reck M, Rodríguez-Abreu D, Robinson AG, et al. Pembrolizumab versus Chemotherapy for PD-L1-Positive Non-Small-Cell Lung Cancer. N Engl J Med. 2016;375:1823-33.
  • 19. Aguilar E, Ricciuti B, Gainor J, et al. Outcomes to first-line pembrolizumab in patients with non-small-cell lung cancer and very high PD-L1 expression. Ann Oncol. 2019;30:1653-59.
  • 20. Cafaro A, Foca F, Nanni O, et al. Real-World Safety and Outcome of First-Line Pembrolizumab Monotherapy for Metastatic NSCLC with PDL-1 Expression ≥ 50%: A National Italian Multicentric Cohort ("PEMBROREAL" Study). Cancers (Basel). 2024;16:1802.
  • 21. Cavazzoni A, Digiacomo G, Volta F, et al. PD-L1 overexpression induces STAT signaling and promotes the secretion of pro-angiogenic cytokines in non-small cell lung cancer (NSCLC). Lung Cancer. 2024;187:107438.
  • 22. Hu B, Chen W, Zhang Y, et al. 18F-FDG maximum standard uptake value predicts PD-L1 expression on tumor cells or tumor infiltrating immune cells in non-small cell lung cancer. Ann Nucl Med 2020;34:322-8.
  • 23. Hu B, Xiao J, Xiu Y, et al. Correlation of PD-L1 expression on tumor cell and tumor infiltrating immune cell with 18F-fluorodeoxyglucose uptake on PET/computed tomography in surgically resected pulmonary adenocarcinoma. Nucl Med Commun 2020; 41:252–9.
  • 24. Monaco L, De Bernardi E, Bono F, et al. The "digital biopsy" in non-small cell lung cancer (NSCLC): a pilot study to predict the PD-L1 status from radiomics features of [18F]FDG PET/CT. Eur J Nucl Med Mol Imaging. 2022;49:3401-11.
  • 25. Xu X, Li J, Yang Y, et al. The correlation between PD-L1 expression and metabolic parameters of 18FDG PET/CT and the prognostic value of PD-L1 in non-small cell lung cancer. Clin Imaging. 2022;89:120-7.
  • 26. Norikane T, Ishimura M, Mitamura K, et al. Texture Features of 18F-Fluorodeoxyglucose Positron Emission Tomography for Predicting Programmed Death-Ligand-1 Levels in Non-Small Cell Lung Cancer. J Clin Med. 2024;13:1625.
  • 27. Li J, Ge S, Sang S, et al. Evaluation of PD-L1 Expression Level in Patients With Non-Small Cell Lung Cancer by 18F-FDG PET/CT Radiomics and Clinicopathological Characteristics. Front Oncol. 2021;11:789014.
  • 28. Cui, Y., and X. Li. PD-L1 in Lung Adenocarcinoma: Insights into the Role of 18F-FDG PET/CT. Cancer Manag Res. 2020;12:6385-95.
  • 29. Wu X, Huang Y, Zhao Q, et al. PD-L1 expression correlation with metabolic parameters of FDG PET/CT and clinicopathological characteristics in non-small cell lung cancer. EJNMMI Res. 2020;10:51.
  • 30. Wang D, Li Y, Chen X, et al. Prognostic significance of volume-based 18F-FDG PET/CT parameters and correlation with PD-L1 expression in patients with surgically resected lung adenocarcinoma. Medicine (Baltimore). 2021;100:e27100.
There are 30 citations in total.

Details

Primary Language English
Subjects Radiology and Organ Imaging
Journal Section Clinical Research
Authors

Özge Vural Topuz 0000-0001-7197-5866

Esranur Acar 0009-0009-8747-3188

Nur Büyükpınarbaşılı 0000-0002-1784-6665

Sefa Bayram 0000-0001-5144-0741

Burcu Esen Akkas 0000-0001-6623-1600

Meryem Kaya 0000-0002-3328-8173

Early Pub Date December 10, 2024
Publication Date January 1, 2025
Submission Date September 14, 2024
Acceptance Date November 19, 2024
Published in Issue Year 2025

Cite

EndNote Vural Topuz Ö, Acar E, Büyükpınarbaşılı N, Bayram S, Akkas BE, Kaya M (January 1, 2025) Baseline 18F FDG PET/CT imaging in NSCLC: Possible utility in predicting strong-positive PD-L1 expression. Acıbadem Üniversitesi Sağlık Bilimleri Dergisi 16 1 164–173.