References
Roy L, Cowden Dahl KD (2018) Can stemness and chemoresistance be therapeutically targeted via signaling pathways in ovarian cancer? Cancers 10:241. https://doi.org/10.3390/cancers10080241
Donatello D, Battista G, Sassi C (2023) Imaging of ovarian lymphoma. J Ultrasound 26:799–807. https://doi.org/10.1007/s40477-023-00779-3
Becker M (2022) Swarm learning for decentralized healthcare. Hautarzt 73(4):323–325. https://doi.org/10.1007/s00105-021-04940-z
Bhardwaj T, Mittal R, Upadhyay H, Lagos L (2022) Applications of swarm intelligent and deep learning algorithms for image-based cancer recognition. In: Garg L, Basterrech S, Banerjee C, Sharma TK (eds) Artificial intelligence in healthcare advanced technologies and societal change. Springer, Singapore
de PinhoPinheiro CA, Nedjah N, de MacedoMourelle L (2020) Detection and classification of pulmonary nodules using deep learning and swarm intelligence. Multimed Tools Appl 79:15437–15465. https://doi.org/10.1007/s11042-019-7473-z
Macedo M, Santana M, dos Santos WP, Menezes R, Bastos-Filho C (2021) Breast cancer diagnosis using thermal image analysis: A data-driven approach based on swarm intelligence and supervised learning for optimized feature selection. Appl Soft Comput. https://doi.org/10.1016/j.asoc.2021.107533
Rosenberg LB et al. (2018) Artificial swarm intelligence employed to amplify diagnostic accuracy in radiology. In: 2018 IEEE 9th annual information technology, electronics and mobile communication conference (IEMCON). 1186–1191. https://doi.org/10.1109/IEMCON.2018.8614883
Al-Rifaie MM, Aber A, Hemanth DJ (2015) Deploying swarm intelligence in medical imaging identifying metastasis, micro-calcifications and brain image segmentation. IET Syst Biol 9(6):234–244. https://doi.org/10.1049/iet-syb.2015.0036
Cai Y, Sharma A (2021) Swarm intelligence optimization: an exploration and application of machine learning technology. J Intell Syst 30(1):460–469. https://doi.org/10.1515/jisys-2020-0084
Jan YT, Tsai PS, Huang WH et al (2023) Machine learning combined with radiomics and deep learning features extracted from CT images: a novel AI model to distinguish benign from malignant ovarian tumors. Insights Imaging 14:68. https://doi.org/10.1186/s13244-023-01412
Cai G, Huang F, Gao Y, Li X, Chi J, Xie J, Zhou L, Feng Y, Huang H, Deng T, Zhou Y, Zhang C, Luo X, Xie X, Gao Q, Zhen X, Liu J (2024) Artificial intelligence-based models enabling accurate diagnosis of ovarian cancer using laboratory tests in China: a multicentre, retrospective cohort study. Lancet Digit Health 6(3):e176–e186. https://doi.org/10.1016/S2589-7500(23)00245-5
Mitchell S, Nikolopoulos M, El-Zarka A, Al-Karawi D, Al-Zaidi S, Ghai A, Gaughran JE, Sayasneh A (2024) Artificial intelligence in ultrasound diagnoses of ovarian cancer: a systematic review and meta-analysis. Cancers 16:422. https://doi.org/10.3390/cancers16020422
Saldanha OL, Quirke P, West NP, James JA et al (2022) Swarm learning for decentralized artificial intelligence in cancer histopathology. Nat Med 28(6):1232–1239. https://doi.org/10.1038/s41591-022-01768-5
Al-Tashi Q, Saad MB, Sheshadri A, Wu CC, Chang JY, Al-Lazikani B, Gibbons C, Vokes NI, Zhang J, Lee JJ, Heymach JV, Jaffray D, Mirjalili S, Wu J (2023) SwarmDeepSurv: swarm intelligence advances deep survival network for prognostic radiomics signatures in four solid cancers. Patterns (N Y) 4(8):F100777. https://doi.org/10.1016/j.patter.2023.100777
Warnat-Herresthal S, Schultze H, Shastry KL et al (2021) Swarm Learning for decentralized and confidential clinical machine learning. Nature 594:265–270. https://doi.org/10.1038/s41586021-03583-3
Gonzales A, Guruswamy G, Smith SR (2023) Synthetic data in health care: a narrative review. PLoS Digit Health 2(1):e0000082. https://doi.org/10.1371/journal.pdig.0000082
Shah R, AstutoAroucheNunes B, Gleason T et al (2023) Utilizing a digital swarm intelligence platform to improve consensus among radiologists and exploring its applications. J Digit Imaging 36:401–413. https://doi.org/10.1007/s10278-022-00662-3
Majumder S, Katz S, Kontos D, Roshkovan L (2024) State of the art: radiomics and radiomics-related artificial intelligence on the road to clinical translation. BJR Open 6(1):tzad004. https://doi.org/10.1093/bjro/tzad004
Mayerhoefer ME, Materka A, Langs G, Häggström I, Szczypiński P, Gibbs P, Cook G (2020) Introduction to radiomics. J Nucl Med 61(4):488–495. https://doi.org/10.2967/jnumed.118.222893
Liberto JM, Chen SY, Shih IM, Wang TH, Wang TL, Pisanic TR 2nd (2022) Current and emerging methods for ovarian cancer screening and diagnostics: a comprehensive review. Cancers (Basel) 14(12):2885. https://doi.org/10.3390/cancers14122885
Takeyama N, Sasaki Y, Ueda Y, Tashiro Y, Tanaka E, Nagai K, Morioka M, Ogawa T, Tate G, Hashimoto T, Ohgiya Y (2024) Magnetic resonance imaging-based radiomics analysis of the differential diagnosis of ovarian clear cell carcinoma and endometrioid carcinoma: a retrospective study. Jpn J Radiol 42(7):731–743. https://doi.org/10.1007/s11604-024-01545-z
Sala E, Mema E, Himoto Y, Veeraraghavan H, Brenton JD, Snyder A, Weigelt B, Vargas HA (2017) Unravelling tumour heterogeneity using next-generation imaging: radiomics, radiogenomics, and habitat imaging. Clin Radiol 72(1):3–10. https://doi.org/10.1016/j.crad.2016.09.013
Crispin-Ortuzar M, Woitek R, Reinius MAV, Moore E, Beer L, Bura V, Rundo L, McCague C, Ursprung S, Escudero Sanchez L, Martin-Gonzalez P, Mouliere F, Chandrananda D, Morris J, Goranova T, Piskorz AM, Singh N, Sahdev A, Pintican R, Zerunian M, Rosenfeld N, Addley H, Jimenez-Linan M, Markowetz F, Sala E, Brenton JD (2023) Integrated radiogenomics models predict response to neoadjuvant chemotherapy in high grade serous ovarian cancer. Nat Commun 14(1):6756. https://doi.org/10.1038/s41467-023-41820-7
Xiao Y, Bi M, Guo H, Li M (2022) Multi-omics approaches for biomarker discovery in early ovarian cancer diagnosis. EBioMedicine 79:104001. https://doi.org/10.1016/j.ebiom.2022.104001
Funding
Not applicable.
Author information
Authors and Affiliations
Contributions
Not applicable.
Corresponding author
Ethics declarations
Conflict of interest
The author declares that she has no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Ethical approval
Not applicable.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Donatello, D. An overview of the use of cutting-edge artificial intelligence (AI) modeling to produce synthetic medical data (SMD) in decentralized clinical machine learning (ML) for ovarian cancer(OC) and ovarian lymphoma(OL). J Ultrasound 28, 483–492 (2025). https://doi.org/10.1007/s40477-025-00983-3
Received:
Accepted:
Published:
Version of record:
Issue date:
DOI: https://doi.org/10.1007/s40477-025-00983-3