Automated PD-L1 status prediction in lung cancer with multi-modal PET/CT fusion.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
19 Jul 2024
Historique:
received: 26 01 2024
accepted: 01 07 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: epublish

Résumé

Programmed death-ligand 1 (PD-L1) expressions play a crucial role in guiding therapeutic interventions such as the use of tyrosine kinase inhibitors (TKIs) and immune checkpoint inhibitors (ICIs) in lung cancer. Conventional determination of PD-L1 status includes careful surgical or biopsied tumor specimens. These specimens are gathered through invasive procedures, representing a risk of difficulties and potential challenges in getting reliable and representative tissue samples. Using a single center cohort of 189 patients, our objective was to evaluate various fusion methods that used non-invasive computed tomography (CT) and

Identifiants

pubmed: 39030240
doi: 10.1038/s41598-024-66487-y
pii: 10.1038/s41598-024-66487-y
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

16720

Subventions

Organisme : This work was partly funded by the ERA-Net CHIST-ERA grant [CHIST-ERA-19-XAI-007] long term challenges in ICT project INFORM
ID : 93603

Informations de copyright

© 2024. The Author(s).

Références

Yu, H., Boyle, T. A., Zhou, C., Rimm, D. L. & Hirsch, F. R. PD-L1 expression in lung cancer. J. Thorac. Oncol. 11, 964–975 (2016).
pubmed: 27117833 pmcid: 5353357 doi: 10.1016/j.jtho.2016.04.014
Huang, G., Liu, Z., Van Der Maaten, L. & Weinberger, K. Q. Densely connected convolutional networks. In IEEE Conference on Computer Vision and Pattern Recognition, 4700–4708 (2017).
Nam, C. H. et al. Temporal evolution of programmed death-ligand 1 expression in patients with non-small cell lung cancer. Korean J. Intern. Med. 36, 975 (2021).
pubmed: 32872743 pmcid: 8273838 doi: 10.3904/kjim.2020.178
Takahashi, T., Tateishi, A., Bychkov, A. & Fukuoka, J. Remarkable alteration of PD-L1 expression after immune checkpoint therapy in patients with non-small-cell lung cancer: Two autopsy case reports. Int. J. Mol. Sci. 20, 2578 (2019).
pubmed: 31130676 pmcid: 6566896 doi: 10.3390/ijms20102578
Socinski, M. et al. Atezolizumab for first-line treatment of metastatic nonsquamous NSCLC. N. Engl. J. Med. 378, 2288–301 (2018).
pubmed: 29863955 doi: 10.1056/NEJMoa1716948
Rossi, S. et al. Clinical characteristics of patient selection and imaging predictors of outcome in solid tumors treated with checkpoint-inhibitors. Eur. J. Nucl. Med. Mol. Imaging 44, 2310–2325 (2017).
pubmed: 28815334 doi: 10.1007/s00259-017-3802-5
Mok, T. et al. Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (keynote-042): A randomised, open-label, controlled, phase 3 trial. Lancet (London England) 393, 1819–30 (2019).
pubmed: 30955977 doi: 10.1016/S0140-6736(18)32409-7
Sun, R. et al. A radiomics approach to assess tumour-infiltrating cd8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy: An imaging biomarker, retrospective multicohort study. Lancet Oncol. 19, 1180–1191 (2018).
pubmed: 30120041 doi: 10.1016/S1470-2045(18)30413-3
Manafi-Farid, R. et al. [18F] FDG-PET/CT radiomics and artificial intelligence in lung cancer: Technical aspects and potential clinical applications. In Seminars in Nuclear Medicine (2022).
Ribas, A. & Wolchok, J. Cancer immunotherapy using checkpoint blockade. Science 359, 1350–5 (2018).
pubmed: 29567705 pmcid: 7391259 doi: 10.1126/science.aar4060
Brody, R. et al. PD-L1 expression in advanced NSCLC: Insights into risk stratification and treatment selection from a systematic literature review. Lung Cancer 112, 200–15 (2017).
pubmed: 29191596 doi: 10.1016/j.lungcan.2017.08.005
Reck, M. et al. Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N. Engl. J. Med. 375, 1823–33 (2016).
pubmed: 27718847 doi: 10.1056/NEJMoa1606774
Scognamiglio, G. et al. Variability in immunohistochemical detection of programmed death ligand 1 (PD-L1) in cancer tissue types. Int. J. Mol. Sci. 17, 790 (2016).
pubmed: 27213372 pmcid: 4881606 doi: 10.3390/ijms17050790
Pinato, D. et al. Intra-tumoral heterogeneity in the expression of programmed-death (PD) ligands in isogeneic primary and metastatic lung cancer: Implications for immunotherapy. Oncoimmunology 5, e1213934 (2016).
pubmed: 27757309 pmcid: 5048760 doi: 10.1080/2162402X.2016.1213934
Hofman, P. PD-L1 immunohistochemistry for non-small cell lung carcinoma: Which strategy should be adopted?. Expert Rev. Mol. Diagn. 17, 1097–108 (2017).
pubmed: 29069958 doi: 10.1080/14737159.2017.1398083
Lambin, P. et al. Radiomics: Extracting more information from medical images using advanced feature analysis. Eur. J. Cancer 48, 441–446 (2012).
pubmed: 22257792 pmcid: 4533986 doi: 10.1016/j.ejca.2011.11.036
Sollini, M., Cozzi, L., Antunovic, L., Chiti, A. & Kirienko, M. Pet radiomics in NSCLC: State of the art and a proposal for harmonization of methodology. Sci. Rep. 7, 1–15 (2017).
doi: 10.1038/s41598-017-00426-y
Desseroit, M.-C. et al. Development of a nomogram combining clinical staging with 18 F-FDG PET/CT image features in non-small-cell lung cancer stage I–III. Eur. J. Nucl. Med. Mol. Imaging 43, 1477–1485 (2016).
pubmed: 26896298 pmcid: 5409954 doi: 10.1007/s00259-016-3325-5
Tan, W. et al. Overview of multiplex immunohistochemistry/immunofluorescence techniques in the era of cancer immunotherapy. Cancer Commun. (Lond Engl) 40, 135–53 (2020).
doi: 10.1002/cac2.12023
Savitha, G. & Jidesh, P. A holistic deep learning approach for identification and classification of sub-solid lung nodules in computed tomographic scans. Comput. Electr. Eng. 84, 106626 (2020).
doi: 10.1016/j.compeleceng.2020.106626
Hatt, M. et al. Joint EANM/SNMMI guideline on radiomics in nuclear medicine: Jointly supported by the EANM physics committee and the SNMMI physics, instrumentation and data sciences council. Eur. J. Nucl. Med. Mol. Imaging 50, 352–375 (2023).
pubmed: 36326868 doi: 10.1007/s00259-022-06001-6
Badic, B. et al. Prediction of recurrence after surgery in colorectal cancer patients using radiomics from diagnostic contrast-enhanced computed tomography: A two-center study. Eur. Radiol. 32, 405–414 (2022).
pubmed: 34170367 doi: 10.1007/s00330-021-08104-4
Chen, X. et al. Recent advances and clinical applications of deep learning in medical image analysis. Med. Image Anal. 79, 102444 (2022).
pubmed: 35472844 pmcid: 9156578 doi: 10.1016/j.media.2022.102444
Tan, M. & Le, Q. EfficientNet: Rethinking model scaling for convolutional neural networks. In International Conference on Machine Learning, 6105–6114 (2019).
He, K., Zhang, X., Ren, S. & Sun, J. Deep residual learning for image recognition. In IEEE Conference on Computer Vision and Pattern Recognition, 770–778 (2016).
Conze, P.-H. et al. Abdominal multi-organ segmentation with cascaded convolutional and adversarial deep networks. Artif. Intell. Med. 117, 102109 (2021).
pubmed: 34127239 doi: 10.1016/j.artmed.2021.102109
Wang, C. et al. Non-invasive measurement using deep learning algorithm based on multi-source features fusion to predict PD-L1 expression and survival in NSCLC. Front. Immunol. 13, 828560 (2022).
pubmed: 35464416 pmcid: 9022118 doi: 10.3389/fimmu.2022.828560
Wang, C. et al. Predicting EGFR and PD-L1 status in NSCLC patients using multitask AI system based on CT images. Front. Immunol. 13, 297 (2022).
Wang, C. et al. Deep learning to predict EGFR mutation and PD-L1 expression status in non-small-cell lung cancer on computed tomography images. J. Oncol. 2021, 5699385 (2021).
doi: 10.1155/2021/5499385
Baek, S. et al. Deep segmentation networks predict survival of non-small cell lung cancer. Sci. Rep. 2191(1), 17286 (2019).
doi: 10.1038/s41598-019-53461-2
Quanyang, W. et al. Artificial intelligence in lung cancer screening: Detection, classification, prediction, and prognosis. Cancer Med. 13(7), e7140 (2024).
pubmed: 38581113 pmcid: 10997848 doi: 10.1002/cam4.7140
Zhu, Y. et al. A CT-derived deep neural network predicts for programmed death ligand-1 expression status in advanced lung adenocarcinomas. Ann. Transl. Med. 8, 930 (2020).
pubmed: 32953730 pmcid: 7475404 doi: 10.21037/atm-19-4690
Han, Y. et al. Histologic subtype classification of non-small cell lung cancer using PET/CT images. Eur. J. Nucl. Med. Mol. Imaging 48, 350–360 (2021).
pubmed: 32776232 doi: 10.1007/s00259-020-04771-5
Ju, L. et al. Deep learning features and metabolic tumor volume based on PET/CT to construct risk stratification in non-small cell lung cancer. Acad Radiol. https://doi.org/10.1016/j.acra.2024.04.036 (2024).
doi: 10.1016/j.acra.2024.04.036 pubmed: 38749868
Kawauchi, K. et al. A convolutional neural network-based system to classify patients using FDG PET/CT examinations. BMC Cancer 20, 1–10 (2020).
doi: 10.1186/s12885-020-6694-x
Aonpong, P., Iwamoto, Y., Han, X.-H., Lin, L. & Chen, Y.-W. Genotype-guided radiomics signatures for recurrence prediction of non-small cell lung cancer. IEEE Access 9, 90244–90254 (2021).
doi: 10.1109/ACCESS.2021.3088234
Lin, X. et al. Lung cancer and granuloma identification using a deep learning model to extract 3-dimensional radiomics features in ct imaging. Clin. Lung Cancer 22, 756–766 (2021).
doi: 10.1016/j.cllc.2021.02.004
Huang, W. et al. PET/CT based EGFR mutation status classification of NSCLC using deep learning features and radiomics features. Front. Pharmacol. 27(13), 898529 (2022).
doi: 10.3389/fphar.2022.898529
Mu, R. et al. Non-invasive decision support for NSCLC treatment using PET/CT radiomics. Eur. J. Nucl. Med. Mol. Imaging 11(1), 5228 (2020).
Yin, G. et al. Prediction of EGFR mutation status based on 18F-FDG PET/CT imaging using deep learning-based model in lung adenocarcinoma. Front. Oncol. 11, 709137 (2021).
pubmed: 34367993 pmcid: 8340023 doi: 10.3389/fonc.2021.709137
Mu, W. et al. Non-invasive measurement of PD-L1 status and prediction of immunotherapy response using deep learning of PET/CT images. J. Immunother. Cancer 9(6), e002118 (2021).
pubmed: 34135101 pmcid: 8211060 doi: 10.1136/jitc-2020-002118
Boellaard, R. 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 42(2), 328–54 (2015).
pubmed: 25452219 doi: 10.1007/s00259-014-2961-x
Hatt, M. et al. Joint EANM/SNMMI guideline on radiomics in nuclear medicine: Jointly supported by the EANM physics committee and the SNMMI physics, instrumentation and data sciences council. Eur J. Nucl. Med. Mol. Imaging 50(2), 352–375 (2023).
pubmed: 36326868 doi: 10.1007/s00259-022-06001-6
Ronneberger, O., Fischer, P. & Brox, T. U-Net: Convolutional networks for biomedical image segmentation. In Medical Image Computing and Computer-Assisted Intervention, 234–241 (2015).
Armato, S. G. et al. The lung image database consortium (LIDC) and image database resource initiative (IDRI): A completed reference database of lung nodules on CT scans. J. Appl. Clin. Med. Phys. 38, 915–931 (2011).
Hatt, M. et al. A fuzzy locally adaptive bayesian segmentation approach for volume determination in pet. IEEE Trans. Med. Imaging 28, 881–893 (2009).
pubmed: 19150782 pmcid: 2912931 doi: 10.1109/TMI.2008.2012036
Da-ano, R. et al. Performance comparison of modified combat for harmonization of radiomic features for multicenter studies. Sci. Rep. 10, 10248 (2020).
pubmed: 32581221 pmcid: 7314795 doi: 10.1038/s41598-020-66110-w
Pieper, P. et al. 3D slicer. In IEEE International Symposium on Biomedical Imaging: Nano to Macro 632–635 (IEEE, 2004).
He, K. et al. Deep residual learning for image recognition. In Proceedings of the IEEE Conference on Computer Vision and Pattern Recognition 770– 778 (2016).
Huang, G. et al. Densely connected convolutional networks. In Proceedings of the IEEE Conference on Computer Vision and Pattern Recognition 2261–2269 (2017).
Podolsky, M. et al. Evaluation of machine learning algorithm utilization for lung cancer classification based on gene expression levels. Asian Pac. J. Cancer Prev. 17, 835–8 (2016).
pubmed: 26925688 doi: 10.7314/APJCP.2016.17.2.835
Grossmann, P. et al. Defining the biological basis of radiomic phenotypes in lung cancer. Elife 6, e23421 (2017).
pubmed: 28731408 pmcid: 5590809 doi: 10.7554/eLife.23421
Ettinger, D. et al. NCCN guidelines insights: Non-small cell lung cancer, version 2.2021. J. Natl. Compr. Cancer Netw. 19, 254–66 (2021).
doi: 10.6004/jnccn.2021.0013
Huynh, E. et al. Artificial intelligence in radiation oncology. Nat. Rev. Clin. Oncol. 771–781, 835–8 (2020).
Toyokawa, G. et al. Computed tomography features of lung adenocarcinomas with programmed death ligand 1 expression. Clin. Lung Cancer 18, e375-83 (2017).
pubmed: 28385373 doi: 10.1016/j.cllc.2017.03.008
Wu, T. et al. The association between imaging features of TSCT and the expression of PD-L1 in patients with surgical resection of lung adenocarcinoma. Clin. Lung Cancer 20, e195-207 (2019).
pubmed: 30514666 doi: 10.1016/j.cllc.2018.10.012
Ardila, D. et al. End-to-end lung cancer screening with three-dimensional deep learning on low-dose chest computed tomography. Nat. Med. 25, 954–961 (2019).
pubmed: 31110349 doi: 10.1038/s41591-019-0447-x
Lu, M. et al. Deep learning using chest radiographs to identify high-risk smokers for lung cancer screening computed tomography: Development and validation of a prediction model. Ann. Intern. Med. 173, 704–713 (2020).
pubmed: 32866413 pmcid: 9200444 doi: 10.7326/M20-1868
Arbour, K. et al. Deep learning to estimate RECIST in patients with NSCLC treated with PD-1 blockade. Cancer Discov. 11, 1 (2020).
Hanna, N. et al. Systemic therapy for stage iv non-small-cell lung cancer: American Society of Clinical Oncology clinical practice guideline update. J. Clin. Oncol. 35, 3484–515 (2017).
pubmed: 28806116 doi: 10.1200/JCO.2017.74.6065
Akamine, T. et al. Association of preoperative serum CRP with PD-L1 expression in 508 patients with non-small cell lung cancer: A comprehensive analysis of systemic inflammatory markers. Surg. Oncol. 27, 88–94 (2018).
pubmed: 29549910 doi: 10.1016/j.suronc.2018.01.002
Lan, B. et al. Association between PD-L1 expression and driver gene status in non-small-cell lung cancer: A meta-analysis. Oncotarget 9, 7684–99 (2018).
pubmed: 29484144 pmcid: 5800936 doi: 10.18632/oncotarget.23969
Jiang, M. et al. Assessing PD-L1 expression level by radiomic features from PET/CT in nonsmall cell lung cancer patients: An initial result. Acad Radiol. 27, 171–9 (2020).
pubmed: 31147234 doi: 10.1016/j.acra.2019.04.016

Auteurs

Ronrick Da-Ano (R)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France.

Gustavo Andrade-Miranda (G)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France.

Olena Tankyevych (O)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France.
Nuclear Medicine, University of Poitiers, Poitiers, France.

Dimitris Visvikis (D)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France. dimitris@univ-brest.fr.

Pierre-Henri Conze (PH)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France.
IMT Atlantique, Brest, France.

Catherine Cheze Le Rest (CCL)

LaTIM, UMR 1101, Inserm, University of Brest, Brest, France.
Nuclear Medicine, University of Poitiers, Poitiers, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH