Evidence map›Paper›PMID 38875514›Full record

ArticleJCO clinical cancer informatics2024

MOSAIC: An Artificial Intelligence-Based Framework for Multimodal Analysis, Classification, and Personalized Prognostic Assessment in Rare Cancers.

Saverio D'Amico, Lorenzo Dall'Olio, Cesare Rollo, Patricia Alonso, Iñigo Prada-Luengo, Daniele Dall'Olio, Claudia Sala, Elisabetta Sauta, Gianluca Asti, Luca Lanino and 21 more

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Molecular-Based Ecosystem to Improve Personalized Medicine in Chronic Myelomonocytic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  4. Review
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  6. Review
  7. Article
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  10. Machine learning is changing osteoporosis detection: an integrative review.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
    Review
  11. Characterization and Clinical Implications of p53 Dysfunction in Patients With Myelodysplastic Syndromes.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Article
  12. Review
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Saverio D'AmicoHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0003-1877-8497
Lorenzo Dall'OlioDepartment of Physics and Astronomy (DIFA), Bologna, Italy.ORCID 0000-0002-8907-0034
Cesare RolloComputational Biomedicine Unit, Department of Medical Sciences, University of Turin, Turin, Italy.
Patricia AlonsoDepartment of Signals, Systems and Radiocommunications, Polytechnic University of Madrid, Madrid, Spain.ORCID 0000-0002-8604-9758
Iñigo Prada-LuengoUniversity of Copenhagen, Copenhagen, Denmark.
Daniele Dall'OlioDepartment of Physics and Astronomy (DIFA), Bologna, Italy.ORCID 0000-0003-0196-6870
Claudia SalaExperimental, Diagnostic and Specialty Medicine-DIMES, Bologna, Italy.ORCID 0000-0002-4889-1047
Elisabetta SautaHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0002-7830-988X
Gianluca AstiHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0009-0006-9078-6482
Luca LaninoHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0003-2404-8829
Giulia MaggioniHumanitas Clinical and Research Center-IRCCS, Milan, Italy.
Alessia CampagnaHumanitas Clinical and Research Center-IRCCS, Milan, Italy.
Elena ZazzettiHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0009-0002-7234-9482
Mattia DelleaniHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0009-0004-1136-0930
Maria Elena BicchieriHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0001-9674-9304
Pierandrea MorandiniHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0002-8615-3766
Victor SavevskiHumanitas Clinical and Research Center-IRCCS, Milan, Italy.
Borja ArroyoDepartment of Signals, Systems and Radiocommunications, Polytechnic University of Madrid, Madrid, Spain.
Juan ParrasDepartment of Signals, Systems and Radiocommunications, Polytechnic University of Madrid, Madrid, Spain.ORCID 0000-0002-7028-3179
Lin Pierre ZhaoHematology and Bone Marrow Transplantation, Hôpital Saint-Louis/University Paris 7, Paris, France.ORCID 0000-0001-5035-4470
Uwe PlatzbeckerMedical Clinic and Policlinic 1, Hematology and Cellular Therapy, University Hospital Leipzig, Leipzig, Germany.ORCID 0000-0003-1863-3239
Maria Diez-CampeloHematology Department, Hospital Universitario de Salamanca, Salamanca, Spain.ORCID 0000-0002-1467-6779
Valeria SantiniHematology, Azienda Ospedaliero-Universitaria Careggi & University of Florence, Florence, Italy.ORCID 0000-0002-5439-2172
Pierre FenauxHematology and Bone Marrow Transplantation, Hôpital Saint-Louis/University Paris 7, Paris, France.
Torsten HaferlachMLL Munich Leukemia Laboratory, Munich, Germany.
Anders KroghUniversity of Copenhagen, Copenhagen, Denmark.
Santiago ZazoDepartment of Signals, Systems and Radiocommunications, Polytechnic University of Madrid, Madrid, Spain.
Piero FariselliComputational Biomedicine Unit, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID 0000-0003-1811-4762
Tiziana SanaviaComputational Biomedicine Unit, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID 0000-0003-3288-0631
Matteo Giovanni Della PortaHumanitas Clinical and Research Center-IRCCS, Milan, Italy.ORCID 0000-0002-6915-5970
Gastone CastellaniDepartment of Physics and Astronomy (DIFA), Bologna, Italy.ORCID 0000-0003-4892-925X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRare cancers constitute over 20% of human neoplasms, often affecting patients with unmet medical needs. The development of effective classification and prognostication systems is crucial to improve the decision-making process and drive innovative treatment strategies. We have created and implemented MOSAIC, an artificial intelligence (AI)-based framework designed for multimodal analysis, classification, and personalized prognostic assessment in rare cancers. Clinical validation was performed on myelodysplastic syndrome (MDS), a rare hematologic cancer with clinical and genomic heterogeneities.

methodsWe analyzed 4,427 patients with MDS divided into training and validation cohorts. Deep learning methods were applied to integrate and impute clinical/genomic features. Clustering was performed by combining Uniform Manifold Approximation and Projection for Dimension Reduction + Hierarchical Density-Based Spatial Clustering of Applications with Noise (UMAP + HDBSCAN) methods, compared with the conventional Hierarchical Dirichlet Process (HDP). Linear and AI-based nonlinear approaches were compared for survival prediction. Explainable AI (Shapley Additive Explanations approach [SHAP]) and federated learning were used to improve the interpretation and the performance of the clinical models, integrating them into distributed infrastructure.

resultsUMAP + HDBSCAN clustering obtained a more granular patient stratification, achieving a higher average silhouette coefficient (0.16) with respect to HDP (0.01) and higher balanced accuracy in cluster classification by Random Forest (92.7% ± 1.3% and 85.8% ± 0.8%). AI methods for survival prediction outperform conventional statistical techniques and the reference prognostic tool for MDS. Nonlinear Gradient Boosting Survival stands in the internal (Concordance-Index [C-Index], 0.77; SD, 0.01) and external validation (C-Index, 0.74; SD, 0.02). SHAP analysis revealed that similar features drove patients' subgroups and outcomes in both training and validation cohorts. Federated implementation improved the accuracy of developed models.

conclusionMOSAIC provides an explainable and robust framework to optimize classification and prognostic assessment of rare cancers. AI-based approaches demonstrated superior accuracy in capturing genomic similarities and providing individual prognostic information compared with conventional statistical methods. Its federated implementation ensures broad clinical application, guaranteeing high performance and data protection.

Indexed as

Artificial IntelligencePrecision MedicineAgedAlgorithmsCluster AnalysisDeep LearningFemaleHumansMaleMiddle AgedMyelodysplastic SyndromesNeoplasmsPrognosisRare Diseases

Identifiers

PMID38875514
PMCPMC11371092

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.