Evidence map›Paper›PMID 38937291›Full record

ArticleSkeletal radiology2025

Whole-body low-dose computed tomography in patients with newly diagnosed multiple myeloma predicts cytogenetic risk: a deep learning radiogenomics study.

Shahriar Faghani, Mana Moassefi, Udit Yadav, Francis K Buadi, Shaji K Kumar, Bradley J Erickson, Wilson I Gonsalves, Francis I Baffour

Abstract read
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Article in Skeletal radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shahriar FaghaniDepartment of Radiology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Mana MoassefiDepartment of Radiology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Udit YadavDivision of Hematology, Mayo Clinic, 13400 E. Shea Blvd, Scottsdale, AZ, 85259, USA.
Francis K BuadiDivision of Hematology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Shaji K KumarDivision of Hematology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Bradley J EricksonDepartment of Radiology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Wilson I GonsalvesDivision of Hematology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA.
Francis I BaffourDepartment of Radiology, Mayo Clinic, 200 1st St SW, Rochester, MN, 55905, USA. baffour.francis@mayo.edu.

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Yi Lin · 2015 to 2026
$25.5M
Assessment of Metabolites Among Asymptomatic Precursor and Malignant Monoclonal GammopathiesR01CA254961 · NCI · MAYO CLINIC ROCHESTER · PI GONSALVES, WILSON · 2021 to 2024
$1.5M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA254961
6 · The paper itself

Abstract

objectiveTo develop a whole-body low-dose CT (WBLDCT) deep learning model and determine its accuracy in predicting the presence of cytogenetic abnormalities in multiple myeloma (MM). MATERIALS AND

methodsWBLDCTs of MM patients performed within a year of diagnosis were included. Cytogenetic assessments of clonal plasma cells via fluorescent in situ hybridization (FISH) were used to risk-stratify patients as high-risk (HR) or standard-risk (SR). Presence of any of del(17p), t(14;16), t(4;14), and t(14;20) on FISH was defined as HR. The dataset was evenly divided into five groups (folds) at the individual patient level for model training. Mean and standard deviation (SD) of the area under the receiver operating curve (AUROC) across the folds were recorded.

resultsOne hundred fifty-one patients with MM were included in the study. The model performed best for t(4;14), mean (SD) AUROC of 0.874 (0.073). The lowest AUROC was observed for trisomies: AUROC of 0.717 (0.058). Two- and 5-year survival rates for HR cytogenetics were 87% and 71%, respectively, compared to 91% and 79% for SR cytogenetics. Survival predictions by the WBLDCT deep learning model revealed 2- and 5-year survival rates for patients with HR cytogenetics as 87% and 71%, respectively, compared to 92% and 81% for SR cytogenetics.

conclusionA deep learning model trained on WBLDCT scans predicted the presence of cytogenetic abnormalities used for risk stratification in MM. Assessment of the model's performance revealed good to excellent classification of the various cytogenetic abnormalities.

Indexed as

Deep LearningIn Situ Hybridization, FluorescenceMultiple MyelomaTomography, X-Ray ComputedAdultAgedAged, 80 and overChromosome AberrationsFemaleHumansMaleMiddle AgedPredictive Value of TestsRadiation DosageRetrospective StudiesRisk AssessmentCT skeletal surveyCytogenetic riskMultiple myeloma

Identifiers

PMID38937291
PMCPMC11652250

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