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Comparison of the ADNEX and ROMA risk prediction models for the diagnosis of ovarian cancer: a multicentre external validation in patients who underwent surgery.
Landolfo, Chiara; Ceusters, Jolien; Valentin, Lil; Froyman, Wouter; Van Gorp, Toon; Heremans, Ruben; Baert, Thaïs; Wouters, Roxanne; Vankerckhoven, Ann; Van Rompuy, Anne-Sophie; Billen, Jaak; Moro, Francesca; Mascilini, Floriana; Neumann, Adam; Van Holsbeke, Caroline; Chiappa, Valentina; Bourne, Tom; Fischerova, Daniela; Testa, Antonia; Coosemans, An; Timmerman, Dirk; Van Calster, Ben.
Afiliação
  • Landolfo C; Department of Oncology, Laboratory of Tumour Immunology and Immunotherapy, Leuven Cancer Institute, KU Leuven, Leuven, Belgium.
  • Ceusters J; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Valentin L; Queen Charlotte's and Chelsea Hospital, Imperial College, London, UK.
  • Froyman W; Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Van Gorp T; Department of Oncology, Laboratory of Tumour Immunology and Immunotherapy, Leuven Cancer Institute, KU Leuven, Leuven, Belgium.
  • Heremans R; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Baert T; Department of Obstetrics and Gynecology, Skåne University Hospital, Malmö, Sweden.
  • Wouters R; Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
  • Vankerckhoven A; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Van Rompuy AS; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
  • Billen J; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
  • Moro F; Department of Oncology, Gynaecological Oncology, KU Leuven, Leuven Cancer Institute, Leuven, Belgium.
  • Mascilini F; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Neumann A; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
  • Van Holsbeke C; Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
  • Chiappa V; Department of Oncology, Gynaecological Oncology, KU Leuven, Leuven Cancer Institute, Leuven, Belgium.
  • Bourne T; Department of Oncology, Laboratory of Tumour Immunology and Immunotherapy, Leuven Cancer Institute, KU Leuven, Leuven, Belgium.
  • Fischerova D; Oncoinvent AS, Oslo, Norway.
  • Testa A; Department of Oncology, Laboratory of Tumour Immunology and Immunotherapy, Leuven Cancer Institute, KU Leuven, Leuven, Belgium.
  • Coosemans A; Department of Pathology, UZ Leuven, Leuven, Belgium.
  • Timmerman D; Department of Laboratory Medicine, UZ Leuven, Leuven, Belgium.
  • Van Calster B; Dipartimento Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Br J Cancer ; 130(6): 934-940, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38243011
ABSTRACT

BACKGROUND:

Several diagnostic prediction models to help clinicians discriminate between benign and malignant adnexal masses are available. This study is a head-to-head comparison of the performance of the Assessment of Different NEoplasias in the adneXa (ADNEX) model with that of the Risk of Ovarian Malignancy Algorithm (ROMA).

METHODS:

This is a retrospective study based on prospectively included consecutive women with an adnexal tumour scheduled for surgery at five oncology centres and one non-oncology centre in four countries between 2015 and 2019. The reference standard was histology. Model performance for ADNEX and ROMA was evaluated regarding discrimination, calibration, and clinical utility.

RESULTS:

The primary analysis included 894 patients, of whom 434 (49%) had a malignant tumour. The area under the receiver operating characteristic curve (AUC) was 0.92 (95% CI 0.88-0.95) for ADNEX with CA125, 0.90 (0.84-0.94) for ADNEX without CA125, and 0.85 (0.80-0.89) for ROMA. ROMA, and to a lesser extent ADNEX, underestimated the risk of malignancy. Clinical utility was highest for ADNEX. ROMA had no clinical utility at decision thresholds <27%.

CONCLUSIONS:

ADNEX had better ability to discriminate between benign and malignant adnexal tumours and higher clinical utility than ROMA. CLINICAL TRIAL REGISTRATION clinicaltrials.gov NCT01698632 and NCT02847832.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Doenças dos Anexos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Doenças dos Anexos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Br J Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica