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.
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“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]
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MRI-Based Radiomics for Outcome Stratification in Pediatric Osteosarcoma
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Decoding Immunodeficiencies with Artificial Intelligence: A New Era of Precision Medicine
Sciaccotta, R., Barone, P., Murdaca, G., Fazio, M., Stagno, F., Gangemi, S., Genovese, S., & Allegra, A. (2025) · Biomedicines · doi:10.3390/biomedicines13081836 · Cited by 4
“Mass spectrometry (MS) is the most precise method for determining the immunopeptidome [39,59].”
Guardamagna, M., Zamorano, E., Albarrán-Artahona, V., Mesas, A., & Benítez, J. C. (2025) · Cancers · doi:10.3390/cancers17132244 · Cited by 5
“Machine learning (ML) programs—a subset of AI—can learn from data to identify patterns and generate predictive models, thus providing a comprehensive analysis of histopathological samples through imaging features to assist in diagnosis and prognosis [16,17].”
Zhu, J., & Ning, Y. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1586130 · Cited by 4
Zhou, C., Zhang, Y., Yang, Z.-J., Huang, Y.-Q., & Da, M.-X. (2025) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v17.i5.106103 · Cited by 4
“Sun et al [37] developed a radiomics signature consisting of eight variables to identify CD8+ T cells, which was subsequently validated against the gene expression signature of CD8+ T cells in the Cancer Genome Atlas dataset, resulting in an AUC value of 0.67.”
InfluentialInvestigating tumor immunogenicity as a determinant of differential abscopal effects
Jeong, Y., Lee, K.-J., Kim, Y. J., Lee, S.-J., Koom, W., Lee, I. J., & Kim, K. (2025) · Journal of Radiation Research · doi:10.1093/jrr/rraf021 · Cited by 4
“Assessing tumor immunogenicity has historically been challenging; however, recent advancements have shown that radiomic features derived from computed tomography imaging can predict CD8 + T-cell infiltration [20].”
Beylergil, V., Collins, L. E., Schwartz, L. H., Eche, T., Zhao, B., Champiat, S., Carvajal, R. D., Abedin, S. E., & Dercle, L. (2025) · European Journal of Cancer · doi:10.1016/j.ejca.2025.115386 · Cited by 3
Self-citationPeng, K., Zhang, X., Li, Z.-L., Wang, Y.-C., Sun, H.-W., Zhao, W., Pan, J., Zhang, X.-Y., Wu, X., Yu, X.-R., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1493735 · Cited by 4
Wang, Y.-N., Guan, F.-D., Wang, S.-Y., Jian, W.-W., & Khan, M. K. (2024) · Precision Radiation Oncology · doi:10.1002/pro6.1244 · Cited by 4
“Sun et al. 17 correlated noninvasive radiomics features to quantitative tumor infiltration of CD8 T cells.”
Chen, Y.-Z., Meng, Z.-S., Zhang, Y.-N., & Xiang, Z.-L. (2024) · Academic Radiology · doi:10.1016/j.acra.2024.10.043 · Cited by 4
Radiomic profiling of high-risk aneurysms with blebs: an exploratory study
Dier, C., Sanchez, S., Sagues, E., Gudino, A., Jaramillo, R., Wendt, L., & Samaniego, E. (2024) · Journal of NeuroInterventional Surgery · doi:10.1136/jnis-2024-022133 · Cited by 4
“40 Previous studies have demonstrated that wall enhancement correlates with histological inflammatory changes, with blebs showing a tendency to capture more contrast.”
Han, Y., Chang, Y., Wang, J., Li, N., Yu, Y., Yang, Z.-B., Lv, W., Liu, W., Yin, J., & Wu, J. (2024) · World Journal of Surgical Oncology · doi:10.1186/s12957-024-03466-7 · Cited by 4
“CT-based radiomics has been demonstrated to aid in predicting treatment responses and outcomes for various cancers [14–16].”
BackgroundGao, X.-Y., Chen, H.-Y., Wang, Y., Xu, F., Zhang, A.-N., Yang, Y., & Gu, Y.-J. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1429115 · Cited by 4
Yu, Y., Guo, H.-W., Zhang, M., Hou, F., Yang, S.-F., Huang, C.-C., Duan, L., & Wang, H.-X. (2024) · Cancer Imaging · doi:10.1186/s40644-024-00705-8 · Cited by 4
“Radiomics can be regarded as a “digital biopsy” that allows in-depth analysis of spatial heterogeneity and tumor phenotypes in various clinical scenarios [29, 30].”
BackgroundA Glimpse Into the Future for Unresectable Stage III Non-Small Cell Lung Cancer
Bartolomeo, V., Cortiula, F., Hendriks, L. E. L., Ruysscher, D. D., & Filippi, A. R. (2023) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2023.11.005 · Cited by 4
Cai, C., Hu, T., Rong, Z., Gong, J., & Tong, T. (2023) · European Journal of Radiology · doi:10.1016/j.ejrad.2023.111254 · Cited by 4
Research status and progress of radiomics in bone and soft tissue tumors: A review
Zhang, X., Peng, J., Ji, G.-H., Li, T., Li, B., & Xiong, H. (2023) · Medicine · doi:10.1097/md.0000000000036198 · Cited by 4
Gu, J., Bao, S., Akemuhan, R., Jia, Z., Zhang, Y., & Huang, C. (2023) · Molecular Imaging and Biology · doi:10.1007/s11307-023-01870-1 · Cited by 5
“All selected images were resampled to a voxel size of 1 × 1 × 1 mm 3 to meet standardization; then, a fixed bin width of 25 HU helped reduce image noise, gaining all tumour images with isotropic resolution [24, 25].”
Yang, W., Wu, W., Wang, L., Zhang, S., Zhao, J.-J., & Qiang, Y. (2023) · Comput. Biol. Medicine · doi:10.1016/j.compbiomed.2023.107371 · Cited by 4
Radiotherapy Dose in Patients Receiving Immunotherapy
Fitzgerald, K., & Schoenfeld, J. D. (2023) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2023.03.012 · Cited by 4
Multivariable Risk Modelling and Survival Analysis with Machine Learning in SARS-CoV-2 Infection
Ciarmiello, A., Tutino, F., Giovannini, E., Milano, A., Barattini, M., Yosifov, N., Calvi, D., Setti, M., Sívori, M., Sani, C., et al. (2023) · medRxiv · doi:10.3390/jcm12227164 · Cited by 4
Hang, R., Bai, G., Sun, B., Xu, P., Sun, X., Yan, G., Zhang, W., & Wang, F. (2023) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-023-07909-x · Cited by 6
“It is very important to evaluate the immune status; at the same time, a high-quality article suggests that GZMA can cause tumor cell death through GSDMB, which is a form of immunogenic cell death, and has important value in turning cold tumors into hot tumors [24].”
BackgroundWu, S., Zhang, R., Wan, X.-J., Yao, T., Zhang, Q.-W., Chen, X., & Fan, X.-B. (2023) · Diagnostic and Interventional Radiology · doi:10.5152/dir.2022.21576 · Cited by 4
Gorodetski, B., Becker, P., Baur, A., Hartenstein, A., Rogasch, J., Furth, C., Amthauer, H., Hamm, B., Makowski, M., & Penzkofer, T. (2022) · European Radiology Experimental · doi:10.1186/s41747-022-00296-8 · Cited by 4
“…focused on the primary tumour, e.g. , for differentiating between benign and malignant lung lesions [23, 24] or between primary and secondary tumours [25], survival prediction [26–28], treatment response [29, 30], or predicting lymph node (LN) metastases on the morphology of the primary tumour [7].”
BackgroundQiu, J.-J., Yin, J., Ji, L., Lu, C.-Y., Li, K.-S., Zhang, Y.-G., & Lin, Y.-X. (2022) · Information Processing & Management · doi:10.1016/j.ipm.2022.103046 · Cited by 4
He, L., Li, Z.-H., Yan, L.-X., Chen, X., Sanduleanu, S., Zhong, W., Lambin, P., Ye, Z., Sun, Y.-S., Liu, Y.-L., et al. (2022) · European Radiology · doi:10.1007/s00330-022-08873-6 · Cited by 4
“Notably, this study is one of the few investigations utilising an immune-informed approach to establish a link between underlying pathology and clinical outcomes [11, 19, 30, 32].”
BackgroundMethodInfluentialSchmitt, M., Aussenac, L., Seitlinger, J., Lindner, V., Noël, G., & Antoni, D. (2022) · Cancers · doi:10.3390/cancers14051282 · Cited by 4
Kimura, Y., Masumoto, N., Kanou, A., Fukui, K., Sasada, S., Emi, A., Kadoya, T., Arihiro, K., & Okada, M. (2022) · Surgical oncology · doi:10.1016/j.suronc.2022.101725 · Cited by 4
Lisson, C., Lisson, C., Achilles, S., Mezger, M. F., Wolf, D., Schmidt, S., Thaiss, W. M., Bloehdorn, J., Beer, A., Stilgenbauer, S., et al. (2022) · Cancers · doi:10.3390/cancers14020393 · Cited by 4
(Chemo)Radiotherapy–Immunotherapy Combinations: Time to Get Tailored?
Mondini, M., & Deutsch, E. (2021) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-21-1173 · Cited by 4
Self-citationWu, L.-L., Wang, J., Huang, W., Liu, X., Huang, Y.-Y., Zeng, J., Cui, C., Lu, J.-B., Lin, P., Long, H., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.565755 · Cited by 4
“In previous studies, deep learning of radiomics has shown unique value in diagnosis and prognosis in the assessment of liver fibrosis in chronic hepatitis B (24), access to tumor-infiltrating CD8 cells, and responses to anti-PD-1 or anti-PD-L1 immunotherapy (25) that could predict lymph node metastasis in ESCC and col…”
BackgroundCao, H., Erson-Omay, E., Gunel, M., Moliterno, J., & Fulbright, R. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.600327 · Cited by 4
“Through advanced MR imaging method and radiomics analysis, the pre-operative genotype (3), immune phenotype (4), and prognosis prediction (5) become possible.”
MethodEditorial: Multi-omic Data Integration in Oncology
Finotello, F., Calura, E., Risso, D., Hautaniemi, S., & Romualdi, C. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01768 · Cited by 4
“In addition, important information can be exploited by integrating omics data and biomedical images (9), a field that is experiencing new advances in terms of sensitivity and resolution.”
BackgroundRadiomics: A Path Forward to Predict Immunotherapy Response in Non-Small Cell Lung Cancer.
Yousefi, B., Katz, S., & Roshkovan, L. (2020) · Radiology: Artificial Intelligence · doi:10.1148/ryai.2020200075 · Cited by 4
Radiomics to predict response to immunotherapy: an imminent reality?
Limkin, E., & Sun, R. (2020) · Future Oncology · doi:10.2217/fon-2020-0015 · Cited by 4
Self-citationAre radiomics ready for clinical prime-time in PET/CT imaging?
Rest, C. C. L., & Hustinx, R. (2019) · The Quarterly Journal of Nuclear Medicine and Molecular Imaging · doi:10.23736/s1824-4785.19.03210-2 · Cited by 5
Battistella, E., Vakalopoulou, M., Estienne, T., Lerousseau, M., Sun, R., Robert, C., Nikos Paragios, A., & Deutsch, É. (2019) · Lecture notes in computer science · doi:10.1007/978-3-030-17938-0_41 · Cited by 5
Self-citationWang, T., Xu, W., & Wu, X. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1882195 · Cited by 3
“PD-L1 expression re fl ects one axis of immune regulation, TMB estimates antigenic potential, CD8 + T-cell density indicates cytotoxic in fi ltra-tion, and ctDNA re fl ects tumor burden or molecular residual disease (37).”
Liu, C., Hu, C., Cheng, J., Xin, D., Jin, S., Tian, W., Li, S., Jin, Y., Liu, Y., Wu, W., et al. (2026) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-013305 · Cited by 2
“Recent studies have used omics data and machine learning methods to identify novel biomarkers and immune cell markers, 4 5 thereby effectively predicting patient responses to ICI therapy.”
Influence of CT harmonization in longitudinal radiomics for NSCLC immunotherapy response prediction
Farina, B., Vegas-Sánchez-Ferrero, G., Ramos-Guerra, A. D., Miras, C. P., Peral, A. A., Merino, J. A., Zugazagoitia, J., Peces-Barba, G., Maceiras, L., Paz-Ares, L., et al. (2026) · Comput. Biol. Medicine · doi:10.1016/j.compbiomed.2026.111501 · Cited by 3
Identification of symptomatic carotid plaque by CTA-based radiomics: a multicenter study
Zhang, W., Wang, Z., Xu, Q., Wang, X., Zhang, L., Chen, R., Liao, M., & Zhong, J.-Q. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1750076 · Cited by 3
Yoo, S. A., & Lee, J. H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110729 · Cited by 3
He, G.-Z., Lai, L.-R., Yu, G., Pang, H.-W., Yu, X., Zhang, H., Zhu, Q., & Lv, Y. (2025) · JMIR Medical Informatics · doi:10.2196/73162 · Cited by 3
Wang, C., Li, Y.-X., Ji, Y., Yu, K., Qin, C., Liu, L., Shuai, Y.-J., Chen, J.-H., Li, A., & Zhang, T. (2025) · Academic Radiology · doi:10.1016/j.acra.2025.09.037 · Cited by 3
Zhong, H., Zhang, H.-H., Wu, J., Zhao, X., Dan, Y.-C., Li, J., Li, L., Luo, M.-P., Xu, Y., Xu, B., et al. (2025) · Current Medical Science · doi:10.1007/s11596-025-00117-0 · Cited by 3
“Concurrently, CT imaging has been widely adopted to predict immune markers such as PD-L1 expression [17, 18] and CD8+ tumor-infiltrating lymphocytes (TILs) [19].”
Chae, Y. K., Velcheti, V., Zhang, K., Hiremath, A., Chung, L. I., Maghsoudi, O. H., Chitalia, R., Lee, J., Li, H., Lee, S., et al. (2026) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-013391 · Cited by 4
Early and hereditary breast cancer: advances in risk stratification and imaging approaches
Cortiana, V., Kannan, S., Vallabhaneni, H., Gambill, J., Nadar, S., Rangrej, V. J. K., Park, C., & Leyfman, Y. (2025) · Therapeutic Advances in Medical Oncology · doi:10.1177/17588359251349677 · Cited by 3
“141 The reliance on small, homogeneous datasets for training radiomic and AI models limits their applicability to diverse patient populations.”
Jiang, H., Zhou, L.-J., Zhang, Q., Yu, T., & Yu, Z. (2025) · Medical Physics (Lancaster) · doi:10.1002/mp.18028 · Cited by 3
“44 These results illustrate how radiomic features can capture both the physical characteristics and underlying biological processes of tumors.”
Jeong, D. Y., Joe, C., Lee, S.-M., Park, S., Moon, S. H., Choi, J. Y., Kim, J., Lee, S.-H., & Lee, H.-Y. (2025) · Comput. Methods Programs Biomed. · doi:10.1016/j.cmpb.2025.108915 · Cited by 3
Zhang, Z., Liang, S.-Y., Zheng, D., Wang, S., Zhou, J., Wang, Z., Huang, Y., Chang, C., Wang, Y.-Y., Guo, Y., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083525 · Cited by 3
“Recently, radiomics has emerged as an innovative method to explore the relationship between imaging features of tumors and their gene expression to predict immunotherapy response [11,12].”
Artificial Intelligence for Drug Discovery: An Update and Future Prospects
Howell, H. J., McGale, J., Choucair, A., Shirini, D., Aide, N., Postow, M. A., Wang, L., Tordjman, M., Lopci, E., Lecler, A., et al. (2025) · Seminars in Nuclear Medicine · doi:10.1053/j.semnuclmed.2025.01.004 · Cited by 7
Self-citationXu, J.-W., Li, B., & Yu, D. (2024) · Hepatoma Research · doi:10.20517/2394-5079.2024.79 · Cited by 1
Xie, W.-T., Jiang, S., Xin, F.-J., Jiang, Z.-N., Pan, W., Zhou, X.-M., Xiang, S., Xu, Z., Lu, Y., & Wang, D.-S. (2024) · Medical Physics (Lancaster) · doi:10.1002/mp.17350 · Cited by 3
“25 As the diversity of cancer types will add difficulty to model training, we hypothesized that radiological pre-CT-BASED dictors focused on a single kind of cancer may have a better performance.”
Lever, M., Bogner, S., Giousmas, M., Mairinger, F., Baba, H., Richly, H., Gromke, T., Schuler, M., Bechrakis, N., & Kalkavan, H. (2024) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.13184 · Cited by 3
“Successful applications were reported in many clinical settings, in particular high incidence oncological entities, for example, for lung cancer (Aerts et al., 2014; Sun et al., 2018).”
Yan, Y., He, X., Xu, Y., Zhao, F., Peng, J., & Shao, Y. (2024) · Age and Ageing · doi:10.1093/ageing/afae140 · Cited by 4
Wang, J., Tang, S., Wu, J., Xu, S., Sun, Q., Zhou, Z., Xu, X., Liu, Y., Liu, Q., Mao, Y., et al. (2024) · Clinical and Translational Gastroenterology · doi:10.14309/ctg.0000000000000712 · Cited by 2
“Image preprocessing included standardizing voxel spacing by resampling images to a voxel size of 1 3 1 3 1 mm and reducing image noise and normalizing intensities by discretizing voxel intensity values with a fi xed-width bin of 25 Houns fi eld units (22,23).”
MethodGao, Y., Wu, R.-M., Pei, Z.-J., Ke, C.-B., Zeng, D.-B., Li, X., & Zhang, Y. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28794 · Cited by 3
Wang, Z., Han, S.-G., Xu, K.-L., Yang, Q., Wang, X.-H., Tang, Y., Shao, Y.-K., & Ye, Y. (2023) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.16366 · Cited by 3
“10 Cheng et al . reported that an enhanced rim of colorectal cancer liver metastasis lesion on the portal venous phase on CE-MDCT could predict the response to bevacizumab-based chemotherapy.”
BackgroundSelf-citationHigh expression of centromere protein N as novel biomarkers for gastric adenocarcinoma
Wang, X.-J., Zhang, K., Fu, C., Wu, F., Zhang, J., Han, B., Pan, H., & Luan, L. (2023) · Cancer Reports · doi:10.1002/cnr2.1798 · Cited by 3
“Immune cell infiltration has been linked to the development and spread of cancer.(31,32) In this study, we explored the association between CENP-N expression and immune cell infiltration in STAD.”
BackgroundImmune checkpoint inhibition: a future guided by radiology
Khan, F., Jones, K. I., & Lyon, P. C. (2023) · British Journal of Radiology · doi:10.1259/bjr.20220565 · Cited by 4
He, W.-Z., Huang, H.-S., Chen, X.-Y., Yu, J.-Q., Liu, J., Li, X., Yin, H., Zhang, K., & Peng, L.-Q. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.1096422 · Cited by 3
Basic premises: searching for new targets and strategies in diffuse gliomas
Sansone, G., Vivori, N., Vivori, C., Stefano, A. L. D., & Pïcca, A. (2022) · Clinical and Translational Imaging · doi:10.1007/s40336-022-00507-7 · Cited by 3
“Seminal works on solid tumours demonstrated that radiomic analyses may be leveraged to predict immune microenvironment features relevant to clinical practice (as the level of tumour infiltrating CD8 lymphocytes [189]).”
BackgroundPredictors of Toxicity Among Older Adults with Cancer.
Extermann, M., Chetty, I., Brown, S., Al-Jumayli, M., & Movsas, B. (2022) · Seminars in Radiation Oncology · doi:10.1016/j.semradonc.2021.11.004 · Cited by 3
Guiard, E., Baldini, C., Pobel, C., Assi, T., Bernard-Tessier, A., Martin-Romano, P., Hollebecque, A., Verlingue, L., Géraud, A., Michot, J., et al. (2022) · European Journal of Cancer · doi:10.1016/j.ejca.2022.02.024 · Cited by 3
Self-citationLin, J., Lin, J.-P., Weng, Y., Lv, C.-B., Chen, J., Zhan, C., Li, P., Xie, J., Wang, J.-B., Lü, J., et al. (2022) · Annals of Surgical Oncology · doi:10.1245/s10434-022-11499-z · Cited by 4
“Radiomics can achieve a comprehensive assessment of the tumor phenotype by using high-throughput imaging features that can provide more internal tumor information than TNM stage, such as changes in cellular and genetic levels.(11) In this study, we confirmed that the prognostic value of the RISS was independent of TNM…”
Result
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
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