Development and validation of a model that includes two ultrasound parameters and the plasma D-dimer level for predicting malignancy in adnexal masses: an observational study

被引:12
|
作者
Stukan, Maciej [1 ,2 ]
Badocha, Michal [3 ,4 ]
Ratajczak, Karol [5 ]
机构
[1] Pomeranian Hosp, Gdynia Oncol Ctr, Dept Gynecol Oncol, Gdynia, Poland
[2] Ul Powstania Styczniowego 1, PL-81519 Gdynia, Poland
[3] Gdansk Univ Technol, Dept Phys Chem, Gdansk, Poland
[4] Ul Gabriela Narutowicza 11-12, PL-80233 Gdansk, Poland
[5] Karol Ratajczak Consulting, Ul Damroki 1A, PL-80175 Gdansk, Poland
关键词
Ovarian cancer; Ultrasound; D-dimer; Calculation; Diagnosis; differential; Sensitivity and specificity; LOGISTIC-REGRESSION MODELS; OVARIAN-CANCER; PREOPERATIVE EVALUATION; VENOUS THROMBOEMBOLISM; DISCRIMINATING BENIGN; SUBJECTIVE ASSESSMENT; MATHEMATICAL-MODELS; POOR-PROGNOSIS; SIMPLE-RULES; DIAGNOSIS;
D O I
10.1186/s12885-019-5629-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPre-operative discrimination of malignant from benign adnexal masses is crucial for planning additional imaging, preparation, surgery and postoperative care. This study aimed to define key ultrasound and clinical variables and develop a predictive model for calculating preoperative ovarian tumor malignancy risk in a gynecologic oncology referral center. We compared our model to a subjective ultrasound assessment (SUA) method and previously described models.MethodsThis prospective, single-center observational study included consecutive patients. We collected systematic ultrasound and clinical data, including cancer antigen 125, D-dimer (DD) levels and platelet count. Histological examinations served as the reference standard. We performed univariate and multivariate regressions, and Bayesian information criterion (BIC) to assess the optimal model. Data were split into 2 subsets: training, for model development (190 observations) and testing, for model validation (n=100).ResultsAmong 290 patients, 52% had malignant disease, including epithelial ovarian cancer (72.8%), metastatic disease (14.5%), borderline tumors (6.6%), and non-epithelial malignancies (4.6%). Significant variables were included into a multivariate analysis. The optimal model, included three independent factors: solid areas, the color score, and the DD level. Malignant and benign lesions had mean DD values of 2.837 and 0.354g/ml, respectively. We transformed established formulae into a web-based calculator (http://gin-onc-calculators.com/gynonc.php) for calculating the adnexal mass malignancy risk. The areas under the curve (AUCs) for models compared in the testing set were: our model (0.977), Simple Rules risk calculation (0.976), Assessment of Different NEoplasias in the adneXa (ADNEX) (0.972), Logistic Regression 2 (LR2) (0.969), Risk of Malignancy Index (RMI) 4 (0.932), SUA (0.930), and RMI3 (0.912).ConclusionsTwo simple ultrasound predictors and the DD level (also included in a mathematical model), when used by gynecologist oncologist, discriminated malignant from benign ovarian lesions as well or better than other more complex models and the SUA method. These parameters (and the model) may be clinically useful for planning adequate management in the cancer center. The model needs substantial validation.
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页数:12
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