Publication:
Radiomics analysis of bone marrow biopsy locations in [18F]FDG PET/CT images for measurable residual disease assessment in multiple myeloma.

dc.contributor.authorMilara, Eva
dc.contributor.authorAlonso, Rafael
dc.contributor.authorMasseing, Lena
dc.contributor.authorSeiffert, Alexander P
dc.contributor.authorGómez-Grande, Adolfo
dc.contributor.authorGómez, Enrique J
dc.contributor.authorMartínez-López, Joaquín
dc.contributor.authorSánchez-González, Patricia
dc.contributor.funderUniversidad Politécnica de Madrid (España)es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderUnión Europea. Fondo Social Europeo (ESF/FSE)
dc.contributor.funderUnión Europea. Comisión Europea. European Aid to the Most Deprived (FEAD)es_ES
dc.contributor.funderCOVITECH-CM (Plataforma cientifico-tecnologica para alerta, diagnostico, pronostico, terapia y seguimiento de la enfermedad COVID19 y futuras pandemias)es_ES
dc.contributor.funderConferencia de Rectores de las Universidades Españolas
dc.contributor.funderConsejo Superior de Investigaciones Científicas (España)
dc.date.accessioned2024-01-22T13:15:35Z
dc.date.available2024-01-22T13:15:35Z
dc.date.issued2023-06
dc.description.abstractThe combination of visual assessment of whole body [18F]FDG PET images and evaluation of bone marrow samples by Multiparameter Flow Cytometry (MFC) or Next-Generation Sequencing (NGS) is currently the most common clinical practice for the detection of Measurable Residual Disease (MRD) in Multiple Myeloma (MM) patients. In this study, radiomic features extracted from the bone marrow biopsy locations are analyzed and compared to those extracted from the whole bone marrow in order to study the representativeness of these biopsy locations in the image-based MRD assessment. Whole body [18F]FDG PET of 39 patients with newly diagnosed MM were included in the database, and visually evaluated by experts in nuclear medicine. A methodology for the segmentation of biopsy sites from PET images, including sternum and posterior iliac crest, and their subsequent quantification is proposed. First, starting from the bone marrow segmentation, a segmentation of the biopsy sites is performed. Then, segmentations are quantified extracting SUV metrics and radiomic features from the [18F]FDG PET images and are evaluated by Mann-Whitney U-tests as valuable features differentiating PET+/PET- and MFC+ /MFC- groups. Moreover, correlation between whole bone marrow and biopsy sites is studied by Spearman ρ rank. Classification performance of the radiomics features is evaluated applying seven machine learning algorithms. Statistical analyses reveal that some images features are significant in PET+/PET- differentiation, such as SUVmax, Gray Level Non-Uniformity or Entropy, especially with a balanced database where 16 of the features show a p value < 0.001. Correlation analyses between whole bone marrow and biopsy sites results in significant and acceptable coefficients, with 11 of the variables reaching a correlation coefficient greater than 0.7, with a maximum of 0.853. Machine learning algorithms demonstrate high performances in PET+/PET- classification reaching a maximum AUC of 0.974, but not for MFC+/MFC- classification. The results demonstrate the representativeness of sample sites as well as the effectiveness of extracted features (SUV metrics and radiomic features) from the [18F]FDG PET images in MRD assessment in MM patients.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThe author E.M. received financial support through a predoctoral Fellowship (ayuda del Programa Propio de I+D+i 2020) from Universidad Politecnica de Madrid. The project was partially supported by COVITECH-CM (Plataforma cientifico-tecnologica para alerta, diagnostico, pronostico, terapia y seguimiento de la enfermedad COVID19 y futuras pandemias) and REACT-UE through the European Regional Development Fund (ERDF), the European Social Fund (EFS) and the Fund for European Aid to the Most Deprived (FEAD).Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. The authors declare that no funds, grants, or other support were received during the preparation of this manuscriptes_ES
dc.format.number2es_ES
dc.format.page903es_ES
dc.format.volume46es_ES
dc.identifier.citationPhys Eng Sci Med. 2023;46(2):903-913.es_ES
dc.identifier.doi10.1007/s13246-023-01265-0es_ES
dc.identifier.e-issn2662-4737es_ES
dc.identifier.journalPhysical and engineering sciences in medicinees_ES
dc.identifier.pubmedID37155114es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17253
dc.language.isoenges_ES
dc.publisherNature Publishing Group
dc.relation.publisherversionhttps://doi.org/10.1007/s13246-023-01265-0.es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Unidades técnicas::Unidad de Investigación Clínica de Tumores Hematológicos H12O-CNIOes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshBone Marrowes_ES
dc.subject.meshMultiple Myelomaes_ES
dc.subject.meshHumanses_ES
dc.subject.meshFluorodeoxyglucose F18es_ES
dc.subject.meshPositron Emission Tomography Computed Tomographyes_ES
dc.subject.meshBiopsyes_ES
dc.titleRadiomics analysis of bone marrow biopsy locations in [18F]FDG PET/CT images for measurable residual disease assessment in multiple myeloma.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
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