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Sökning: WFRF:(Franchi Dorella) > (2020-2024) > Multiclass risk mod...

Multiclass risk models for ovarian malignancy : an illustration of prediction uncertainty due to the choice of algorithm

Ledger, Ashleigh (författare)
Catholic University of Leuven
Ceusters, Jolien (författare)
Catholic University of Leuven,Leuven Cancer Institute
Valentin, Lil (författare)
Lund University,Lunds universitet,Obstetrisk, gynekologisk och prenatal ultraljudsdiagnostik,Forskargrupper vid Lunds universitet,Obstetric, Gynaecological and Prenatal Ultrasound Research,Lund University Research Groups,Skåne University Hospital
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Testa, Antonia (författare)
Catholic University of the Sacred Heart, Rome,Policlinico Universitario Agostino Gemelli
Van Holsbeke, Caroline (författare)
Hospital Oost-Limburg
Franchi, Dorella (författare)
European Institute of Oncology
Bourne, Tom (författare)
Queen Charlotte's and Chelsea Hospital,Catholic University of Leuven,University Hospitals Leuven
Froyman, Wouter (författare)
University Hospitals Leuven,Catholic University of Leuven
Timmerman, Dirk (författare)
University Hospitals Leuven,Catholic University of Leuven
Van Calster, Ben (författare)
Catholic University of Leuven,Leiden University Medical Centre
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 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: BMC Medical Research Methodology. - 1471-2288. ; 23:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Assessing malignancy risk is important to choose appropriate management of ovarian tumors. We compared six algorithms to estimate the probabilities that an ovarian tumor is benign, borderline malignant, stage I primary invasive, stage II-IV primary invasive, or secondary metastatic. Methods: This retrospective cohort study used 5909 patients recruited from 1999 to 2012 for model development, and 3199 patients recruited from 2012 to 2015 for model validation. Patients were recruited at oncology referral or general centers and underwent an ultrasound examination and surgery ≤ 120 days later. We developed models using standard multinomial logistic regression (MLR), Ridge MLR, random forest (RF), XGBoost, neural networks (NN), and support vector machines (SVM). We used nine clinical and ultrasound predictors but developed models with or without CA125. Results: Most tumors were benign (3980 in development and 1688 in validation data), secondary metastatic tumors were least common (246 and 172). The c-statistic (AUROC) to discriminate benign from any type of malignant tumor ranged from 0.89 to 0.92 for models with CA125, from 0.89 to 0.91 for models without. The multiclass c-statistic ranged from 0.41 (SVM) to 0.55 (XGBoost) for models with CA125, and from 0.42 (SVM) to 0.51 (standard MLR) for models without. Multiclass calibration was best for RF and XGBoost. Estimated probabilities for a benign tumor in the same patient often differed by more than 0.2 (20% points) depending on the model. Net Benefit for diagnosing malignancy was similar for algorithms at the commonly used 10% risk threshold, but was slightly higher for RF at higher thresholds. Comparing models, between 3% (XGBoost vs. NN, with CA125) and 30% (NN vs. SVM, without CA125) of patients fell on opposite sides of the 10% threshold. Conclusion: Although several models had similarly good performance, individual probability estimates varied substantially.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Calibration
Machine learning
Multiclass models
Ovarian Neoplasms
Prediction models

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

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