The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
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
Abstract
Background Because responses of patients with cancer to immunotherapy can vary in success, innovative predictors of response to treatment are urgently needed to improve treatment outcomes. We aimed to develop and independently validate a radiomics-based biomarker of tumour-infiltrating CD8 cells in patients included in phase 1 trials of anti-programmed cell death protein (PD)-1 or anti-programmed cell death ligand 1 (PD-L1) monotherapy. We also aimed to evaluate the association between the biomarker, and tumour immune phenotype and clinical outcomes of these patients. Methods In this retrospective multicohort study, we used four independent cohorts of patients with advanced solid tumours to develop and validate a radiomic signature predictive of immunotherapy response by combining contrast-enhanced CT images and RNA-seq genomic data from tumour biopsies to assess CD8 cell tumour infiltration. To develop the radiomic signature of CD8 cells, we used the CT images and RNA sequencing data of 135 patients with advanced solid malignant tumours who had been enrolled into the MOSCATO trial between May 1, 2012, and March 31, 2016, in France (training set). The genomic data, which are based on the CD8B gene, were used to estimate the abundance of CD8 cells in the samples and data were then aligned with the images to generate the radiomic signatures. The concordance of the radiomic signature (primary endpoint) was validated in a Cancer Genome Atlas [TGCA] database dataset including 119 patients who had available baseline preoperative imaging data and corresponding transcriptomic data on June 30, 2017. From 84 input variables used for the machine-learning method (78 radiomic features, five location variables, and one technical variable), a radiomics-based predictor of the CD8 cell expression signature was built by use of machine learning (elastic-net regularised regression method). Two other independent cohorts of patients with advanced solid tumours were used to evaluate this predictor. The immune phenotype internal cohort (n=100), were randomly selected from the Gustave Roussy Cancer Campus database of patient medical records based on previously described, extreme tumour-immune phenotypes: immune-inflamed (with dense CD8 cell infiltration) or immune-desert (with low CD8 cell infiltration), irrespective of treatment delivered; these data were used to analyse the correlation of the immune phenotype with this biomarker. Finally, the immunotherapy-treated dataset (n=137) of patients recruited from Dec 1, 2011, to Jan 31, 2014, at the Gustave Roussy Cancer Campus, who had been treated with anti-PD-1 and anti-PD-L1 monotherapy in phase 1 trials, was used to assess the predictive value of this biomarker in terms of clinical outcome. Findings We developed a radiomic signature for CD8 cells that included eight variables, which was validated with the gene expression signature of CD8 cells in the TCGA dataset (area under the curve [AUC]=0·67; 95% CI 0·57-0·77; p=0·0019). In the cohort with assumed immune phenotypes, the signature was also able to discriminate inflamed tumours from immune-desert tumours (0·76; 0·66-0·86; p<0·0001). In patients treated with anti-PD-1 and PD-L1, a high baseline radiomic score (relative to the median) was associated with a higher proportion of patients who achieved an objective response at 3 months (vs those with progressive disease or stable disease; p=0·049) and a higher proportion of patients who had an objective response (vs those with progressive disease or stable disease; p=0·025) or stable disease (vs those with progressive disease; p=0·013) at 6 months. A high baseline radiomic score was also associated with improved overall survival in univariate (median overall survival 24·3 months in the high radiomic score group, 95% CI 18·63-42·1; vs 11·5 months in the low radiomic score group, 7·98-15·6; hazard ratio 0·58, 95% CI 0·39-0·87; p=0·0081) and multivariate analyses (0·52, 0·35-0·79; p=0·0022). Interpretation The radiomic signature of CD8 cells was validated in three independent cohorts. This imaging predictor provided a promising way to predict the immune phenotype of tumours and to infer clinical outcomes for patients with cancer who had been treated with anti-PD-1 and PD-L1. Our imaging biomarker could be useful in estimating CD8 cell count and predicting clinical outcomes of patients treated with immunotherapy, when validated by further prospective randomised trials. Funding Fondation pour la Recherche Médicale, and SIRIC-SOCRATE 2.0, French Society of Radiation Oncology.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“First, previous studies have primarily focused on tumor-infiltrating lymphocytes,12,26 which only provide a simplified and partial view of the TME.”
From Non-invasive tumor microenvironment evaluation and treatment response prediction in gastric cancer using deep learning radiomics (2023) · cites this paper as [12]
In the citing paper
“This idea is motivated by prior work showing that either approach can extract useful information for assessing TME.12,13,33,35”
From Non-invasive tumor microenvironment evaluation and treatment response prediction in gastric cancer using deep learning radiomics (2023) · cites this paper as [12]
In the citing paper
“The feasibility of this idea has been demonstrated in previous studies.12,23,24,25”
From Non-invasive tumor microenvironment evaluation and treatment response prediction in gastric cancer using deep learning radiomics (2023) · cites this paper as [12]
In the citing paper
“Sun et al. developed a radiomic signature of CD8 T cells, which was correlated with clinical response and outcomes of patients treated with anti-PD1 immunotherapy.12”
From Non-invasive tumor microenvironment evaluation and treatment response prediction in gastric cancer using deep learning radiomics (2023) · cites this paper as [12]
Citations
Cites
PD-1 blockade induces responses by inhibiting adaptive immune resistance
Tumeh, P. C., Harview, C. L., Yearley, J. H., Shintaku, I. P., Taylor, E. J. M., Robert, L., Chmielowski, B., Spasic, M., Henry, G., Ciobanu, V., et al. (2014) · Nature · doi:10.1038/nature13954 · Cited by 6,609
Self-citationPembrolizumab plus chemotherapy in metastatic non–small-cell lung cancer
Gandhi, L., Rodríguez-Abreu, D., Gadgeel, S., Esteban, E., Felip, E., De Angelis, F., Domine, M., Clingan, P., Hochmair, M. J., Powell, S. F., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1801005 · Cited by 6,607
Pembrolizumab versus Ipilimumab in Advanced Melanoma
Robert, C., Schachter, J., Long, G. V., Arance, A., Grob, J. J., Mortier, L., Daud, A., Carlino, M. S., McNeil, C., Lotem, M., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1503093 · Cited by 5,887
Self-citationElements of cancer immunity and the cancer–immune set point
Chen, D. S., & Mellman, I. (2017) · Nature · doi:10.1038/nature21349 · Cited by 5,352
Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients
Herbst, R. S., Soria, J.-C., Kowanetz, M., Fine, G. D., Hamid, O., Gordon, M. S., Sosman, J. A., McDermott, D. F., Powderly, J. D., Gettinger, S. N., et al. (2014) · Nature · doi:10.1038/nature14011 · Cited by 5,231
Self-citationDecoding tumour phenotype by noninvasive imaging using a quantitative radiomics approach
Aerts, H. J. W. L., Velazquez, E. R., Leijenaar, R. T. H., Parmar, C., Grossmann, P., Carvalho, S., Bussink, J., Monshouwer, R., Haibe-Kains, B., Rietveld, D., et al. (2014) · Nature Communications · doi:10.1038/ncomms5006 · Cited by 5,132
The Cancer Imaging Archive (TCIA): Maintaining and Operating a Public Information Repository
Clark, K., Vendt, B., Smith, K., Freymann, J., Kirby, J., Koppel, P., Moore, S., Phillips, S., Maffitt, D., Pringle, M., et al. (2013) · Journal of Digital Imaging · doi:10.1007/s10278-013-9622-7 · Cited by 4,599
Durvalumab after chemoradiotherapy in stage III non–small-cell lung cancer
Antonia, S. J., Villegas, A., Daniel, D., Vicente, D., Murakami, S., Hui, R., Yokoi, T., Chiappori, A., Lee, K. H., de Wit, M., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1709937 · Cited by 4,593
Genomic and Transcriptomic Features of Response to Anti-PD-1 Therapy in Metastatic Melanoma
Hugo, W., Zaretsky, J. M., Sun, L., Song, C., Moreno, B. H., Hu-Lieskovan, S., Berent-Maoz, B., Pang, J., Chmielowski, B., Cherry, G., et al. (2016) · Cell · doi:10.1016/j.cell.2016.02.065 · Cited by 3,448
Research works printed but not linked: 41
- Limkin, 2017, Promises and challenges for the implementation of computational medical imaging (radiomics) in oncology, Ann Oncol, 28, 1191, 10.1093/annonc/mdx034 · DOI
- Gillies, 2010, The biology underlying molecular imaging in oncology: from genome to anatome and back again, Clin Radiol, 65, 517, 10.1016/j.crad.2010.04.005 · DOI
- Sun, 2016, In regard to Mattonen et al, Int J Radiat Oncol Biol Phys, 95, 1544, 10.1016/j.ijrobp.2016.03.038 · DOI
- Ansell, 2015, Hodgkin lymphoma: MOPP chemotherapy to PD-1 blockade and beyond, Am J Hematol, 91, 109, 10.1002/ajh.24226 · DOI
- Reck, 2016, Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer, N Engl J Med, 375, 1823, 10.1056/NEJMoa1606774 · DOI · Paper page
- Kim, 2016, Immune escape to PD-L1/PD-1 blockade: seven steps to success (or failure), Ann Oncol, 27, 1492, 10.1093/annonc/mdw217 · DOI · Paper page
- Hegde, 2016, The where, the when, and the how of immune monitoring for cancer immunotherapies in the era of checkpoint inhibition, Clin Cancer Res, 22, 1865, 10.1158/1078-0432.CCR-15-1507 · DOI · Paper page
- Massard, 2017, High-throughput genomics and clinical outcome in hard-to-treat advanced cancers: results of the MOSCATO 01 trial, Cancer Discov, 7, 586, 10.1158/2159-8290.CD-16-1396 · DOI
- Grabowski, 2015, Tumor infiltrating lymphocytes and PD-L1 expression differ in low and high grade neuroendocrine tumors (abstract), Neuroendocrinology, 10, 107
- Crow, 1998, Pathology of uterine fibroids, Baillieres Clin Obstet Gynaecol, 12, 197, 10.1016/S0950-3552(98)80061-8 · DOI
- Champiat, 2017, Hyperprogressive disease is a new pattern of progression in cancer patients treated by anti-PD-1/PD-L1, Clin Cancer Res, 23, 1920, 10.1158/1078-0432.CCR-16-1741 · DOI
- Sun, 2017, Baseline lymphopenia should not be used as exclusion criteria in early clinical trials investigating immune checkpoint blockers (PD-1/PD-L1 inhibitors), Eur J Cancer, 84, 202, 10.1016/j.ejca.2017.07.033 · DOI
- Becht, 2016, Estimating the population abundance of tissue-infiltrating immune and stromal cell populations using gene expression, Genome Biol, 17, 218, 10.1186/s13059-016-1070-5 · DOI
- Weinstein, 2013, The Cancer Genome Atlas Pan-Cancer analysis project, Nat Genet, 45, 1113, 10.1038/ng.2764 · DOI · Paper page
- Sridharan, 2016, Immune profiling of adenoid cystic carcinoma: PD-L2 expression and associations with tumor-infiltrating lymphocytes, Cancer Immunol Res, 4, 679, 10.1158/2326-6066.CIR-16-0031 · DOI
- Hatt, 2015, 18F-FDG PET uptake characterization through texture analysis: investigating the complementary nature of heterogeneity and functional tumor volume in a multi-cancer site patient cohort, J Nucl Med, 56, 38, 10.2967/jnumed.114.144055 · DOI
- Vallières, 2017, Radiomics strategies for risk assessment of tumour failure in head-and-neck cancer, Sci Rep, 7, 10117, 10.1038/s41598-017-10371-5 · DOI
- Nioche, 2017, A freeware for tumor heterogeneity characterization in PET, SPECT, CT, MRI and US to accelerate advances in radiomics, J Nucl Med, 58, S1316
- Leijenaar, 2015, The effect of SUV discretization in quantitative FDG-PET radiomics: the need for standardized methodology in tumor texture analysis, Sci Rep, 5, 11075, 10.1038/srep11075 · DOI
- Patro, 2017, Salmon provides fast and bias-aware quantification of transcript expression, Nat Methods, 14, 417, 10.1038/nmeth.4197 · DOI · Paper page
- Miles, 2009, Colorectal cancer: texture analysis of portal phase hepatic CT images as a potential marker of survival, Radiology, 250, 444, 10.1148/radiol.2502071879 · DOI
- Zou, 2005, Regularization and variable selection via the elastic net, J R Stat Soc Series B Stat Methodol, 67, 301, 10.1111/j.1467-9868.2005.00503.x · DOI · Paper page
- Gutman, 2013, Cancer Digital Slide Archive: an informatics resource to support integrated in silico analysis of TCGA pathology data, J Am Med Inform Assoc, 20, 1091, 10.1136/amiajnl-2012-001469 · DOI
- Arkenau, 2009, Prospective validation of a prognostic score to improve patient selection for oncology phase I trials, J Clin Oncol, 27, 2692, 10.1200/JCO.2008.19.5081 · DOI
- Jayasurya, 2000, Lymphocytic infiltration in undifferentiated nasopharyngeal cancer, Arch Otolaryngol Head Neck Surg, 126, 1329, 10.1001/archotol.126.11.1329 · DOI
- Braman, 2017, Intratumoral and peritumoral radiomics for the pretreatment prediction of pathological complete response to neoadjuvant chemotherapy based on breast DCE-MRI, Breast Cancer Res, 19, 57, 10.1186/s13058-017-0846-1 · DOI
- Galloway, 1975, Texture analysis using gray level run lengths, Computer Graphics and Image Processing, 4, 172, 10.1016/S0146-664X(75)80008-6 · DOI
- Fletcher, 2016, Dealing with uncertainty in CT Images, Radiology, 279, 5, 10.1148/radiol.2016152771 · DOI
- Pao, 2018, Tissue-specific immunoregulation: a call for better understanding of the “immunostat” in the context of cancer, Cancer Discov, 8, 395, 10.1158/2159-8290.CD-17-1320 · DOI
- Teillaud, 2017, Tertiary lymphoid structures: an anti-tumor school for adaptive immune cells and an antibody factory to fight cancer?, Front Immunol, 8, 830, 10.3389/fimmu.2017.00830 · DOI
- Goc, 2014, Tertiary lymphoid structures in human lung cancers, a new driver of antitumor immune responses, Oncoimmunology, 3, e28976, 10.4161/onci.28976 · DOI
- Marvel, 2015, Myeloid-derived suppressor cells in the tumor microenvironment: expect the unexpected, J Clin Invest, 125, 3356, 10.1172/JCI80005 · DOI
- Lanitis, 2017, Mechanisms regulating T-cell infiltration and activity in solid tumors, Ann Oncol, 28, xii18, 10.1093/annonc/mdx238 · DOI · Paper page
- Tumeh, 2017, Liver metastasis and treatment outcome with anti-PD-1 monoclonal antibody in patients with melanoma and NSCLC, Cancer Immunol Res, 5, 417, 10.1158/2326-6066.CIR-16-0325 · DOI
- Tang, 2018, Development of an immune-pathology informed radiomics model for non-small cell lung cancer, Sci Rep, 8, 1922, 10.1038/s41598-018-20471-5 · DOI · Paper page
- Grossmann, 2017, Defining the biological basis of radiomic phenotypes in lung cancer, Elife, 6, e23421, 10.7554/eLife.23421 · DOI · Paper page
- Chen, 2018, Associations of tumor PD-1 ligands, immunohistochemical studies, and textural features in 18F-FDG PET in squamous cell carcinoma of the head and neck, Sci Rep, 8, 105, 10.1038/s41598-017-18489-2 · DOI
- Thorsson, 2018, The immune landscape of cancer, Immunity, 48, 812, 10.1016/j.immuni.2018.03.023 · DOI · Paper page
- Saltz, 2018, Spatial organization and molecular correlation of tumor-infiltrating lymphocytes using deep learning on pathology images, Cell Rep, 23, 181, 10.1016/j.celrep.2018.03.086 · DOI · Paper page
- Davoli, 2017, Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy, Science, 355, eaaf8399, 10.1126/science.aaf8399 · DOI
- Liu, 2018, Tumor-repopulating cells induce PD-1 expression in CD8+ T cells by transferring kynurenine and AhR activation, Cancer Cell, 33, 480, 10.1016/j.ccell.2018.02.005 · DOI · Paper page
Cited by
Sorted by citations
Items 901–1,000 of 1,003
Exceptional Response to PD-1 Blockade as First-Line Therapy in Head and Neck Squamous Cell Carcinoma
Kumai, T., Komatsuda, H., Minami, Y., & Harabuchi, Y. (2020) · ORL · doi:10.1159/000509485 · Cited by 1
He, K., Liu, X., Li, M., Li, X., Yang, H., & Zhang, H. (2020) · doi:10.21203/rs.2.22851/v1 · Cited by 1
“Previous studies have attempted to investigate the relationship between image characteristics and genetic mutations[6, 22, 23] or pathological subtype[24, 25].”
BackgroundRadiomics: A Well-Intentioned Leap of Faith
Cho, C. (2019) · Annals of Surgical Oncology · doi:10.1245/s10434-019-07818-6 · Cited by 1
Biobanques tumorales et gestion des données complexes : enjeux actuels et futurs
Hofman, P. M., Dagher, G., Laurent‐Puig, P., Marquette, C., Barlési, F., Bibeau, F., & Clément, B. (2019) · Annales de Pathologie · doi:10.1016/j.annpat.2019.01.017 · Cited by 3
Hofman, P. (2019) · Precision Cancer Medicine · doi:10.21037/pcm.2019.01.03 · Cited by 1
“The first cohort of 119 patients comes from the cancer project gene atlas or TCGA (7).”
BackgroundMethodInfluentialNuclear medicine and immunotherapy: many questions but not many answers yet
Annunziata, S., & Giordano, A. (2019) · Clinical and translational imaging · doi:10.1007/s40336-018-00312-1 · Cited by 1
“1 3 derived from radiopharmaceuticals; the widespread availability of PET-CT tomographs would theoretically facilitate such an hybrid approach [10].”
BackgroundiBiopsy® for Precision Medicine
Brag, J., Auffret, M., Ramos, C., Liu, Y., & Baudot, P. (2018) · European Medical Journal · doi:10.33590/emj/10310309
Advances in Immunotherapy and Efficacy Prediction for Gastric Cancer
陈, 进. (2024) · Advances in Clinical Medicine · doi:10.12677/acm.2024.1492556 · Cited by 1
Ashenden, S. K., Deswal, S., Bulusu, K. C., Bartosik, A., & Shameer, K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820045-2.00004-0 · Cited by 4
Current practices in oncology drug delivery
Mahendiratta, S., Bansal, S., Kumar, S., Sarma, P., Prakash, A., & Medhi, B. (2021) · Advanced Drug Delivery Systems in the Management of Cancer · doi:10.1016/b978-0-323-85503-7.00006-7 · Cited by 1
Biomedical image characterization and radiogenomics
Fan, M., Zhu, Y., Li, L., Clarke, R. C., & Wang, Y. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816034-3.00018-3 · Cited by 1
Efficacy Considerations in Phase I Trials
Alshammari, K., Taylor, K., & Siu, L. (2020) · Springer eBooks · doi:10.1007/978-3-030-47682-3_10 · Cited by 1
Li, Y., Wang, J., Zhang, Q., Gao, G., & Wang, H.-Y. (2026) · Journal of Radiation Research and Applied Sciences · doi:10.1016/j.jrras.2026.102724
Li, X., Wu, P., & Yin, Y. (2026) · Journal of Radiation Research and Applied Sciences · doi:10.1016/j.jrras.2026.102736
Bertolaccini, L., Chiari, M., Degiovanni, S., Mazzella, A., Iacono, G. L., Guarize, J., Casiraghi, M., & Spaggiari, L. (2026) · Cancers · doi:10.3390/cancers18213415
Li, T.-X., Zou, T., Li, Z., Liu, Z.-L., Chen, J.-C., Xiong, Y.-L., Li, M.-X., Zhang, X.-Q., He, P., Guo, W.-R., et al. (2026) · iScience · doi:10.1016/j.isci.2026.117782
“15,24,25 Zhang et al. also found that texture features reflecting necrotic regions play important roles in predicting pathological response.”
Li, J., Suppiah, S., Kasilingam, L., Hui, S. T., Shi, H., Lee, S. T., Sharin, M. F. M., & Al-Ibraheem, A. (2026) · Frontiers in Medical Engineering · doi:10.3389/fmede.2026.1979078
Akbal, S., Schepers, J. C., Oorth, P. V. O. G., Bleymehl, V., Schroth, M., Winneknecht, F., Machiraju, D., Holzschuh, J., Zhang, K., Wohlfeil, S., et al. (2026) · Cancer Imaging · doi:10.1186/s40644-026-01135-4
Bian, C., Qin, Y., Zou, H., Fan, W., & Li, J. (2026) · Cancers · doi:10.3390/cancers18193218
“Evidence indicates that radiomic features are associated with the HCC immune microenvironment, suggesting that the noninvasive dissection of tumor immune characteristics is feasible [20–22].”
Wu, H., & Chen, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1931388
Shen, X., Liu, Z., Yu, W., Li, F., Lu, Y., Li, M., Sun, P., & Liu, A. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1970256
Multimodal Artificial Intelligence in Lung Cancer: From Data Integration to Precision Oncology
Chakrabarti, T., Mansour, A. G., Wu, X., Arias-Romero, J., Mambetsariev, I., Chang, N., Santos, S. D., Mirzapoiazova, T., Fricke, J., Kim, J., et al. (2026) · Cancers · doi:10.3390/cancers18182953
“As such, Sun and colleagues demonstrated that a machine-learning model which generated a radiomic signature assessing CD8+ T cell infiltration was able to predict immunotherapy response with an AUC of 0.76 across multiple cohorts [97].”
InfluentialMRI‐based radiomics model for predicting VEGFA expression and prognosis in lower‐grade glioma
Zhao, K., Hong, X.-Y., Cheng, H., Xu, S.-C., Zhao, D., Lin, J., Gu, Y.-B., Ren, G.-Q., Chen, B.-M., Zhan, L.-P., et al. (2026) · Medical Physics (Lancaster) · doi:10.1002/mp.70615
“13,14 Recently, radiomics has shown promise 15 in enhancing diagnostic, prognostic, and predictive accuracy within neuro-oncology.”
Spatiotemporal immune heterogeneity and precision immunotherapy for ovarian cancer
Yang, X.-F., Wang, Y.-D., You, H.-Y., Gao, J.-Y., Feng, Y.-K., Zhang, F., Zhang, Y., Zhang, B., Zhao, S.-J., & Gu, Y.-F. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70836
“Treg-associated cluster of differentiation 39 and cluster of differentiation 73 can also contribute to extracellular adenosine generation, creating conditions unfavourable for cytotoxic lymphocyte activity.”
Cao, Y., Guo, K., Wang, D., Wang, Z., & Ren, S. (2026) · Cancer Genetics · doi:10.1016/j.cancergen.2026.09.005
Toulet, A., Seegers, V., Bigot, F., Guillemois, S., Vansteene, D., Delva, R., & de Vries-Brilland, M. (2026) · Cancers · doi:10.3390/cancers18183040
“More comprehensive approaches may therefore improve the distinction between PP and PD. Radiomics offers the possibility of extracting quantitative information related to tumor morphology and heterogeneity from routinely acquired imaging [33,34].”
Tan, Y.-M., Xu, S.-Y., Liu, M., Liu, X.-F., Zhang, C.-L., Liao, W.-W., He, L.-C., Zeng, X.-J., Zhu, R.-K., Shen, M.-H., et al. (2026) · European Journal of Surgical Oncology · doi:10.1016/j.ejso.2026.112151
Longitudinal radiomics of liver metastases during magnetic resonance-guided radiotherapy
Paunoiu, A., Fritsak, M., Gabryś, H., Christ, S., Guckenberger, M., Tanadini-Lang, S., & Bello, R. D. (2026) · Physics and Imaging in Radiation Oncology · doi:10.1016/j.phro.2026.101094
Qin, Q.-J., Hou, M.-Y., Tian, J.-J., Sun, Y.-Z., Jing, X.-H., & Zuo, T.-Y. (2026) · World Journal of Radiology · doi:10.4329/wjr.124658
Mazzaschi, G., Balbi, M., Leo, L., Tor, L. M. D., Rosati, R., Marrocchio, C., Mura, R., Milanese, G., D'Agnelli, S., Bocchialini, G., et al. (2026) · Tumori · doi:10.1177/03008916261462796
“29 Their findings suggest that relatively homogeneous and hypodense tumors and peripheral rings may correlate with high CD8 levels, whereas heterogeneity might instead indicate processes such as chaotic vascularization and necrosis.”
AI-driven dual-task prediction model for co-stratifying efficacy and toxicity in NSCLC immunotherapy
Ding, H., Ren, Y., Ding, S., Chen, Y., Wu, Y., Feng, Y., Xia, W., Song, X., Li, R., Mao, Q., et al. (2026) · PLOS Digital Health · doi:10.1371/journal.pdig.0001568
“Prior studies have demonstrated the feasibility of radiomics or deep-learning models for predicting immunotherapy outcomes [22–24].”
Scott, K., Kim, S., Siraj, J., Geady, C., Boccalon, M., Welch, M. L., Alim, M., Hope, A. J., & Haibe-Kains, B. (2026) · arXiv.org · doi:10.48550/arxiv.2607.28423
“These findings align with emerging evidence supporting the relevance of tumour-stroma interactions [36] and peritumoural radiomics [37, 38] for biologically meaningful prediction tasks.”
Xie, D., Li, Z.-X., Li, J., & Hu, K.-W. (2026) · Medical Review · doi:10.1515/mr-2026-0037
“Although spatial omics and radiomics may eventually support dynamic or non-invasive monitoring, tissue-based pathological validation remains the foundational next step [12].”
Qie, S., Shi, Y., Li, J.-Y., Jia, S.-F., & Yin, X.-P. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1760264
Huang, Y.-C., Huang, S.-M., Yeh, J.-H., & Tu, S.-J. (2026) · Strahlentherapie und Onkologie (Print) · doi:10.1007/s00066-026-02569-2
“In parallel, tumor microenvironmental factors, including stromal composition, hypoxia-related immunosuppression, and immune-cell in-filtration, are recognized contributors to treatment response and cancer prognosis [39–42].”
Lawrance, L., Leguerney, I., Benane-Benatsou, B., Dupont, J., Ammari, S., Bône, A., Balleyguier, C., Choucair, A., Massard, C., Lassau, N., et al. (2026) · European Radiology Experimental · doi:10.1186/s41747-026-00771-6
“Innovative quantitative imaging biomarkers offer a noninvasive alternative to capture global and spatially resolved tumor heterogeneity [13], potentially overcoming biases of purely dimensional assessments, which can be confounded by immune-related phenomena such as pseudoprogression or transient…”
Self-citationPang, C., Ru, J., Liu, Y., Ding, W.-Z., Chai, S., Yao, J.-D., Liu, S.-H., Feng, H., Liu, J., Chen, M., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-74985-y
“Sun et al. proposed a contrast-enhanced CT based radiomics approach to assess tumor-in fi ltrating CD8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy 31 .”
Wen, X., Li, Y., Hu, Y.-D., Chen, A.-Q., Wang, K., Zou, W., Xie, B., & Ma, Y.-C. (2026) · Technology in Cancer Research and Treatment · doi:10.1177/15330338261465744
Liu, J., Gao, X., Ma, T., Li, X., Ye, L., Wang, L., Ding, X., Xiao, J., & Ye, Z. (2026) · Academic Radiology · doi:10.1016/j.acra.2026.06.038
Zhu, B., Chen, K.-H., Wen, Z., Zhu, L.-R., Li, L., & Zhu, X.-D. (2026) · European Journal of Radiology · doi:10.1016/j.ejrad.2026.113112
Tian, F.-F., Chen, L.-L., Chen, X.-L., & Pang, H.-Y. (2026) · Cancer Imaging · doi:10.1186/s40644-026-01074-0
“This critical distinction suggests that pre-treatment imaging may more accurately reflect the fundamental, innate biological properties of the tumor which ultimately dictate long-term survival outcomes [17].”
Dynamic multimodal radiomic model for survival prediction in cervical cancer: a multi-cohort study
Yang, G., Wang, W.-P., Zhang, C.-L., Liu, Y.-L., Yang, S.-L., Dai, J.-J., Xiang, Z.-Y., Zhang, F.-Q., Qiu, J., Yang, B., et al. (2026) · npj Precision Oncology · doi:10.1038/s41698-026-01545-4
“Through systematic analysis of these features, radiomics may provide indirect information related to tumor heterogeneity, aggressiveness, and treatment-associated imaging changes 12 – 14 , thereby supporting personalized radiotherapy decision-making 9,15 .”
Muneer, A., Showkatian, E., Saad, M. B., Hong, L., Li, S.-D., Salehjahromi, M., Aminu, M., Sujit, S., Xu, H., Waqas, M., et al. (2026) · Cancer Letters · doi:10.1016/j.canlet.2026.218687
He, W.-Z., Xiong, Y., Huang, X., Luo, H.-R., Zhou, S.-Q., Tu, Y., Deng, T., & Gu, M. (2026) · Scientific Reports · doi:10.1038/s41598-026-56091-7
Artificial Intelligence and the Evolving Paradigm of Lung Cancer Management
Martins, R. S., Hanna, Y., & Axtell, A. L. (2026) · Cancers · doi:10.3390/cancers18122012
“…growth factor receptor (EGFR) [24] status, lymph node [25] and distant organ [26] metastasis, treatment response and adverse reactions to immunotherapy [27], post-treatment response to immunotherapy [28,29], overall survival after treatment [30,31], and local or distant recurrence [32,33].”
Kothari, G., Hardcastle, N., Perera, R., Jackson, P., Lee, S., Silver, J. D., Gaudreault, M., Li, J., Brown, C., Mitchell, P. L., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-53520-5
“Radiomic models incorporating both intra-tumoural and peri-tumoural features have shown to correlate with CD8 cell tumour infiltration, suggesting that the peri-tumoural microenvironment may provide important information about immune activity 12 .”
InfluentialXie, D., Xu, L.-G., Xu, J.-X., Chen, H.-F., Yu, J.-N., He, C., Qiu, Y.-G., Fu, L.-F., Han, Q., Kong, L., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1795169
Saad, F. F., & Bashara, D. M. (2026) · JOURNAL OF MEDICAL AND HEALTH SCIENCE · doi:10.21070/anamnetic.v4i1.1655
“These representations may be indications of a complex process referred to as "Intratumoral Heterogeneity, known as one of the most important resistance concepts that has been ignored in single-site needle biopsies [45, 46].”
Sánchez, D. I. R., Middelkoop, J., Vanneste, T., Maxouri, O., Ursprung, S., Rostami, S., Bogveradze, N., Chupetlovska, K., Castagnoli, F., Landolfi, F., et al. (2026) · European Radiology · doi:10.1007/s00330-026-12601-9
Gil, D., Sanchez, I., & Sanchez, C. (2026) · doi:10.48550/arxiv.2605.14667
“Mixed-effects modeling has previously been used Sun, Limkin, Vakalopoulou et al. (2018) to include acquisition parameters as factors in regression models for the development of a radiomic signature predicting response to immunotherapy treatments.”
Le, M. N., Nguyen, T. M., Ngô, L. L., Le, T. D., Nguyen, D. A., Nguyen, N., Dinh, H., Le, N., Bùi, T. T. N., & Bui, T. O. (2026) · Cancer Control: Journal of the Moffitt Cancer Cente · doi:10.1177/10732748261455532
“18,19 Earlier studies often viewed the tumor as a single, uniform structure, without accounting for local heterogeneity that could reflect EGFR related molecular differences.”
de-Kermenguy, F., Ellsworth, S. G., Facciabene, A., Durante, M., Pacelli, R., St-Aubin, J., & Wang, D.-X. (2026) · Journal of Applied Clinical Medical Physics · doi:10.1002/acm2.70636
Huang, K., Han, Z.-Q., Xia, Y.-F., Lou, X., Wu, X., Fu, R.-Z., Wu, L.-Y., & Gao, C. (2026) · Translational Cancer Research · doi:10.21037/tcr-2026-1-0308
“Notably, a 2018 article by Sun et al. on radiomics analysis of the TME was the most frequently cited in the co-citation analysis, significantly influencing radiomics research within the TME field (27).”
Zhang, S., Wang, Y., Dai, D., & Xu, W.-G. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1739125
Ma, J., Guo, K.-X., Gao, Y.-P., Li, T., Li, F., Pang, C., Geng, Y., & Guo, J.-W. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1767389
“…low PD-L1 expression and high CD3+ T-cell in fi ltration, consistent with an immune-activated state (33); similarly, radiomic signatures have been reported to discriminate immune-in fl amed from immune-desert tumours and to correlate with CD8-related immune phenotypes and immunotherapy outcomes (34).”
Ye, Y.-Z., Chou, P.-Y., Ou, D., Tai, W.-H., Yu, C.-J., Lin, S.-Y., Chen, Y.-F., Wang, C.-Y., Liu, C.-H., Lee, C.-E., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-49064-3
“For instance, Sun et al. 22 was the first to use radiomics analysis to explore the relationship between immune phenotypes and imaging features across various cancers.”
Cheng, M.-Y., Bai, D., Liu, W.-J., Fan, J., Liang, Y.-Z., Li, W.-F., & Wang, Z.-Q. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1786939
Application of artificial intelligence in lung cancer diagnosis, therapy, and prognosis
Wang, Y., Tian, R., Liu, J., Duan, S., Zhang, Y., & Guo, S. (2026) · BMC Medical Genomics · doi:10.1186/s12920-026-02360-3
“Sun et al. [127] developed a radiomic feature of CD8 T cells that can predict the efficacy of anti-PD-1 or anti-PD-L1 immunotherapy.”
Liu, X., & Lei, J. (2026) · Clinical & Translational Oncology · doi:10.1007/s12094-026-04346-0
“This capability is uniquely valuable for detecting micro-metastases lacking morphological signs [33], thereby facilitating safer preoperative stratification.”
Imaging Immune Heterogeneity in Nasopharyngeal Carcinoma: A Multidimensional Radiomics Perspective.
Liang, J.-X., Wang, Z., & Zhang, Y.-Q. (2026) · Academic Radiology · doi:10.1016/j.acra.2026.03.035
Gao, Q., Zhu, C., Chen, M.-F., Mo, S.-T., He, Y.-F., Huang, K., Liao, Y., Liang, T.-Y., Han, C.-Y., & Peng, T. (2026) · Journal of Hepatocellular Carcinoma · doi:10.2147/jhc.s596500
“17,41,42 All extracted features underwent Z-score normalization to ensure data consistency.”
Yuan, Y., Zhang, Z., Shu, Z., Wei, Y., Song, Q., & Xiang, Y. (2026) · BMC Neurology · doi:10.1186/s12883-026-04779-8
“This process involved standardizing image pixel values to a resolution of 1 × 1 × 1 and adjusting the grayscale to encompass 32 levels [19].”
Wang, J., Jiang, Z.-Y., Ji, W.-H., Cheng, H., Zhang, Z., Dekker, A., Wee, L., Yan, M., & Lai, X.-J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1787518
Yin, X., Wang, Z., Zhao, Q.-X., Zhang, X.-C., Sang, T., & Shao, C.-P. (2026) · Medicine · doi:10.1097/md.0000000000047576
“[14–16] US-based radiomics (US-radiomics) is becoming increasingly popular, although radiomics studies in breast cancer have primarily used MRI or PET/CT. [17,18] US-radiomics US-radiomics can measure tumor heterogeneity, internal echoes, and acoustic texture, which may indirectly reflect…”
Eikenboom, E. L., Magnin, J., Alessandris, R., Horvat, N. D. S. M. R., Gonen, M., Jarnagin, W. R., Drebin, J. A., D'Angelica, M. I., Kingham, T. P., Balachandran, V. P., et al. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2025.1584167
Melanoma Beyond the Microscope in the Era of AI and Integrated Diagnostics
Aksoy, S., Demircioğlu, P., & Böğrekçi, İ. (2026) · Dermato · doi:10.3390/dermato6010006
“Predictive models based on AI are possibly one approach that could efficiently address these challenges by providing an integrated analysis of genomics, epigenomics, and immune parameters for more accurate predictions [78,79].”
Balaji, D. T., & Veeranan, V. A. G. (2026) · International Journal of Integrative Studies (IJIS) · doi:10.63856/wd8eqk05
“In precision oncology, AI-extracted radiomic features are used to match patients with therapies most likely to be effective based on the tumor’s phenotypic signature [19].”
Targeted nanodelivery of CRISPR/Cas9 for hepatocellular carcinoma gene therapy in murine models
Yue, F., Jiang, X., Yang, Y., Jiang, Y., Ma, L., Wang, F., & Luo, J. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.173751
Biomarkers of Immunotherapy Response in Surgical Oncology
Bae, J., & Cohen, S. (2026) · Surgical Oncology Clinics of North America · doi:10.1016/j.soc.2025.12.011
Saber, R., Tonneau, M., Salko, O., Liberman, M., Malo, J., Elkrief, A., Turcotte, S., Bouchard, N., Joubert, P., Kadoury, S., et al. (2026) · Cancers · doi:10.3390/cancers18040552
“Several studies have leveraged radiomics features and machine learning models to predict tumor infiltrating lymphocytes, namely cytotoxic T cells [19] and helper T cells [20] and the intratumoral expression of immune biomarkers [21] including PD-L1 expression [22,23].”
Sang, B., Zang, X., Yu, J., Yang, L., Yang, G., Xiaodan, G., Zheng, M., Qi, H., Qiu, Q., Cao, F., et al. (2026) · Academic Radiology · doi:10.1016/j.acra.2026.01.057
Wang, A.-N., Wang, S.-Y., Zhang, S.-J., Liu, F.-L., Zhou, T.-L., Li, Z.-Q., Wang, Y.-X., Xu, J.-X., Cai, J., Wang, X., et al. (2026) · International Journal of Cancer · doi:10.1002/ijc.70352
Geng, Z., Hu, Y., Zhou, S., Wu, G., Gong, Z., Feng, R., Huang, Z., Mei, P., Li, K., Ye, G., et al. (2026) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-025-04291-x · Cited by 1
Xu, Z., Liu, Y.-W., Ji, Y., Cao, S.-Y., Wang, T., Wu, H.-Y., Tang, W., Wu, X.-F., Xia, Y.-X., Xu, Q., et al. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-025-07627-4
“The “glszm_GrayLevelNonUniformity” measure the variability of gray-level intensity values in the image, with a higher value indicating more heterogeneity in intensity values and intertwined processes within the tumor, such as chaotic vascularization and necrosis [32].”
Crombé, A., Sitruk, L. A., Masson-Grehaigne, C., Lafon, M., Palussière, J., Bonhomme, B., Cousin, S., Lassau, N., & Italiano, A. (2026) · European Radiology · doi:10.1007/s00330-025-12292-8
“…kinase inhibitors, highlighting the potentially predictive value of radiomic heterogeneity, in the context of targeted therapy, consistent with literature data suggesting that tumors with greater spatial heterogeneity may harbor subclonal populations with differential therapeutic sensitivity [26].”
Hou, S., Li, W.-F., Fu, M., Li, Y.-G., Zhao, Y., & Zhang, H.-L. (2026) · Discover Oncology · doi:10.1007/s12672-026-04411-8
“Furthermore, multicenter, large-scale studies have shown that radiomics can predict tumor immunophenotypes, offering a promising approach to assess the efficacy of immune checkpoint treatments such as Programmed Cell Death Protein-1 (PD-1) and Programmed Death-Ligand 1 (PD-L1) [8, 9].”
Ying, H., Huang, L., & Hong, W. (2026) · European Journal of Radiology Open · doi:10.1016/j.ejro.2026.100725
Intelligence artificielle et imagerie thoracique
Chassagnon, G. (2025) · Encyclopédie médico-chirurgicale. Pneumologie · doi:10.1016/s1155-195x(24)46306-8
Xu, T.-M., Feng, J., Zhang, K., Gao, L., & Wang, J. (2026) · Chemical Biology and Drug Design · doi:10.1111/cbdd.70244
“Interestingly, preliminary radiomic and pathomic analyses suggest that imaging features can correlate with in situ immune cell infiltration, an emerging biomarker for predicting prognosis and immunotherapy response (Sun et al. 2018; Pagès et al. 2010; Galon and Lanzi 2020; Banna et al. 2019).”
He, R., Ma, Y.-L., Wu, X.-X., Liu, F., Li, L., Wu, T.-Q., Xu, G.-P., Cheng, C., Zhao, S., & Wu, X.-L. (2025) · Applied intelligence (Boston) · doi:10.1007/s10489-025-06986-1
“These features have been demonstrated to be effective in reflecting subtle features in images and can be employed to identify disease heterogeneity [31 , 32].”
放疗联合免疫治疗在不可切除III期非小细胞肺癌中的临床研究进展及未来展望
Tan, Z., Zhong, Y.-L., Wang, J.-Y., & Wu, L. (2025) · Zhongguo fei ai za zhi = Chinese journal of lung cancer · doi:10.3779/j.issn.1009-3419.2025.102.42
“…: 13.8 vs 6.2 个月, P =0.028 ; mOS :未达到 vs 14.8 个 月, P =0.005 )。这些证据共同提示, ctDNA 阳性是复发高 危标志,同时可精准筛选 ICIs 治疗获益人群。 影像组学作为无创评估工具,在风险分层中展现 独特价值。一项回顾性研究 [62] 显示,高影像组学评分组 的 mOS 显著优于低评分组( 24.3 vs 11.5 个月, HR=0.58 , P =0.0081 )。另一项研究 [63] 则证实,无论 PD-L1 水平如何, 高危影像组学特征均可独立预测 PFS ( P <0.0001 )。一系列 研究 [64,65]…”
InfluentialWu, Z.-R., Chen, W., Li, X.-C., Ruffini, F., Liu, S.-N., Tronchin, L., Albano, D., Faiella, E., Fazzini, D., Santucci, D., et al. (2025) · IEEE journal of biomedical and health informatics · doi:10.1109/jbhi.2025.3618935
“As illustrated in Table I, existing methods typically choose to use feature selection engineering [11] and traditional imputation techniques (e.g. Mean-Mode and KNN) to address the issue of missing values in tabular data.”
Tumor Microenvironment as a Key Target for Immunotherapy in Lung Cancer Patients
Ganina, A., Doskali, M., Zaripova, L., Askarov, M., Muhamedzhanova, P., Brimova, A., Kozina, L., Karimova, M., Berikbol, D., Chuvakova, E., et al. (2025) · Russian Open Medical Journal · doi:10.15275/rusomj.2025.0303
Luo, W., Zhao, B., & Shi, Z.-Y. (2025) · European Urology · doi:10.1016/j.eururo.2025.09.4132
Artificial Intelligence in Cancer Immunotherapy: A Leap towards Precision Medicine
Akbari, M., Sadigh‐Eteghad, S., Bahadori, A., Ghassemi-moghaddam, H., & Ziaee, M. (2025) · مجله دانشگاه علوم پزشکی اردبیل · doi:10.61882/jarums.25.1.7
Deng, L., Zhang, M., Zhu, K., Ren, J.-L., Zhang, P., Zhang, Y.-T., Jing, M., Han, T., Zhang, B., & Zhou, J.-L. (2024) · Academic Radiology · doi:10.1016/j.acra.2024.07.004
Ge, Y., Fan, M., Li, X., Liu, Y.-Y., & Li, L.-H. (2024) · Medical Imaging · doi:10.1117/12.3006685
Che, F., Wei, Y., Xu, Q., Li, Q., Zhang, T., Wang, L., Li, M., Yuan, F., & Song, B. (2024) · Abdominal Radiology · doi:10.1007/s00261-024-04190-2
“In another study, Ferté et al. explored the correlation of radiomics features with the expression of CD8 in solid tumors and showed that the imaging signature may be useful in estimating CD8 cell count and may further help the clinician improve treat-ment selection [30].”
Chen, M., & Aboagye, E. (2024) · Journal of Thoracic Oncology · doi:10.1016/j.jtho.2023.10.019
Py, C., Vito, C. D., Tsantoulis, P. K., Kaya, G., Labidi-Galy, S., & Dietrich, P.-Y. (2023) · Swiss medical weekly · doi:10.57187/s.3504
“This pattern has been associated with a better response to immune checkpoint blockade [32, 33] and chemotherapy [34] in metastatic cancer.”
BackgroundLes outils d’imagerie en oncologie thoracique en 2023
Assié, J., Leleu, O., Olivier, P., & Revel, M. (2023) · Revue des Maladies Respiratoires Actualités · doi:10.1016/s1877-1203(23)00015-0
Translating Data Science Results into Precision Oncology Decisions: A Mini Review
Capobianco, E., & Dominietto, M. D. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12020438
Léost, F., Delpon, G., Garcion, E., Gestin, J., Hatt, M., Potiron, V. A., Rbah‐Vidal, L., & Supiot, S. (2022) · Bulletin du Cancer · doi:10.1016/j.bulcan.2022.06.005
Griazov, A., Griazov, A., Grydina, N., & Stuley, V. (2022) · Український радіологічний та онкологічний журнал · doi:10.46879/ukroj.2.2022.25-40
The Next-Level Precision Medicine in Cancer Management Using Artificial Intelligence.
Tian, J. (2021) · Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih · doi:10.24920/004013
Médecine de précision et immunoradiothérapie
Chargari, C., Robert, C., Genestie, C., & Deutsch, É. (2021) · Cancer/Radiothérapie · doi:10.1016/j.canrad.2021.06.032
Self-citationYang, M.-L., She, Y., Ren, Y.-J., Deng, J.-J., Xie, D., Sun, X.-W., Shi, J., & Chen, C. (2021) · Shanghai Chest · doi:10.21037/shc-20-81
“(52) established a model to predict CD8 expression, which predicted an AUC of 0.”
BackgroundSummers, R. (2021) · Radiology · doi:10.1148/radiol.2021204407
“Sun et al (7) developed a radiomics score that predicted the abundance of CD8 immune cells in tumors.”
BackgroundWolsztynski, E., & Eary, J. (2020) · PET/CT and PET/MR in Melanoma and Sarcoma · doi:10.1007/978-3-030-60429-5_6
Metadata
- Authors
- Sun, R., Limkin, E. J., Vakalopoulou, M., Dercle, L., Champiat, S., Han, S. R., Verlingue, L., Brandao, D., Lancia, A., Ammari, S., Hollebecque, A., Scoazec, J.-Y., Marabelle, A., Massard, C., Soria, J.-C., Robert, C., Paragios, N., Deutsch, E., & Ferté, C.
- Affiliations
- Inserm (FR)
- Université Paris-Saclay (FR)
- Institut Gustave Roussy (FR)
- L'Hôpital Nord Franche-Comté (FR)
- Université Paris-Sud (FR)
- ORCID
- Venue
- The Lancet Oncology
- Publisher
- Elsevier BV
- Published
- 2018-09
- Volume
- 19
- Issue
- 9
- Pages
- 1180-1191
- ISSN
- 1470-2045 (ISSN-L)
- OpenAlex
- W2885326465
- Cited by
- 1,236
- References
- 48
- Citations by year
- 2026: 109 · 2025: 118 · 2024: 186 · 2023: 180 · 2022: 165 · 2021: 221 · 2020: 155 · 2019: 89 · 2018: 9
- FWCI
- 81.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Lancet Oncology (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Fondation pour la Recherche Médicale
- American Society for Radiation Oncology
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Radiomics and Machine Learning in Medical Imaging
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Keywords
- radiomics, anti-PD-1 therapy, PD-L1 blockade, immunotherapy response prediction, imaging biomarkers, advanced solid tumors, contrast-enhanced CT, radiomics signature, elastic net
- MeSH terms
- Antineoplastic Agents, Immunological, Adult, Aged, Female, Humans, Male, Middle Aged, Neoplasms, Phenotype, Predictive Value of Tests, Retrospective Studies, RNA, Neoplasm, Time Factors, Tomography, X-Ray Computed, Biomarkers, Tumor, Reproducibility of Results, Lymphocytes, Tumor-Infiltrating, Treatment Outcome, Sequence Analysis, RNA, CD8-Positive T-Lymphocytes, Gene Expression Profiling, Molecular Imaging, Transcriptome, B7-H1 Antigen, Programmed Cell Death 1 Receptor
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review