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Establishing a prediction model for prostate cancer bone metastasis

机译:建立前列腺癌骨转移的预测模型

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We collected clinical data from 308 prostate cancer (PCa) patients to investigate the clinical characteristics and independent risk factors of bone metastasis (BM) and to establish a prediction model for BM of PCa and determine the necessity of bone scans. Univariate and multivariate analyses were performed based on age, biopsy Gleason score (BGS), clinical tumor stage (cTx), total prostate specific antigen (tPSA), free prostate specific antigen (fPSA), fPSA/tPSA, prostate volume, alkaline phosphatase (ALP), serum calcium and serum phosphorus. Moreover, 80 of the 308 PCa patients had a PI-RADS v2 score and were analysed retrospectively. The univariate analysis showed that the BGS, cTx, tPSA, fPSA, prostate volume and ALP were significant. The multivariate logistic regression analysis showed significant differences among the BGS, cTx, tPSA and ALP. Four cases should be highly suspected with BM: (i) cTl-cT2, BGS ≤7, ALP 120 U/L and tPSA 90.64 ng/ml; (ii) cTl-cT2, BGS ≥8, and ALP 120 U/L; (iii) cT3-cT4, BGS ≤7, and ALP 120 U/L; and (iv) cT3-cT4 and BGS ≥8. After the PI-RADS v2 score was included in the model, the AUC of the prediction model rose from 0.884 (95% CI: 0.813-0.996) to 0.934 (95% CI: 0.883-0.986). This model may help determine the necessity of bone scans to diagnose BM for PCa patients.
机译:我们收集了308例前列腺癌(PCa)患者的临床数据,以研究其临床特征和骨转移(BM)的独立危险因素,并建立PCa BM的预测模型并确定骨扫描的必要性。根据年龄,活检格里森评分(BGS),临床肿瘤分期(cTx),总前列腺特异性抗原(tPSA),游离前列腺特异性抗原(fPSA),fPSA / tPSA,前列腺体积,碱性磷酸酶( ALP),血清钙和血清磷。此外,在308位PCa患者中,有80位具有PI-RADS v2评分,并进行了回顾性分析。单因素分析表明,BGS,cTx,tPSA,fPSA,前列腺体积和ALP显着。多元逻辑回归分析显示BGS,cTx,tPSA和ALP之间存在显着差异。高度怀疑有BM的四个病例:(i)cT1-cT2,BGS≤7,ALP> 120 U / L,tPSA> 90.64 ng / ml; (ii)cT1-cT2,BGS≥8,且ALP> 120 U / L; (iii)cT3-cT4,BGS≤7,且ALP> 120 U / L; (c)cT3-cT4和BGS≥8。在模型中包含PI-RADS v2分数后,预测模型的AUC从0.884(95%CI:0.813-0.996)上升到0.934(95%CI:0.883-0.986)。该模型可以帮助确定进行PCa患者BM诊断的骨扫描的必要性。

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