首页> 外文期刊>BJU international >The ability of prostate-specific antigen (PSA) density to predict an upgrade in Gleason score between initial prostate biopsy and prostatectomy diminishes with increasing tumour grade due to reduced PSA secretion per unit tumour volume
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The ability of prostate-specific antigen (PSA) density to predict an upgrade in Gleason score between initial prostate biopsy and prostatectomy diminishes with increasing tumour grade due to reduced PSA secretion per unit tumour volume

机译:由于每单位肿瘤体积PSA分泌减少,前列腺特异性抗原(PSA)密度预测初始前列腺活检和前列腺切除术之间的Gleason评分升级的能力随肿瘤等级的增加而降低

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OBJECTIVES: ? To analyse the performance of PSA density (PSAD) as a predictor of Gleason score upgrade in a large cohort stratified by Gleason score. ? We and others have shown that an upgrade in Gleason score between initial prostate biopsy and final radical prostatectomy (RP) pathology is a significant risk factor for recurrence after local therapy. PATIENTS AND METHODS: ? Patients undergoing RP with matching biopsy information were identified from two prospective databases. ? Patients were analysed according to the concordance between biopsy and final pathology Gleason score in three paired groups: 6/>6, 3 + 4/>3 + 4, 7/>7. ? Receiver-operating characteristic (ROC) curves were generated stratified by Gleason score, and the area under the curve (AUC) calculated. ? Logistic regression models were fitted to identify significant predictors of tumour upgrade. RESULTS: ? From 1516 patients, 435 (29%) had an upgrade in Gleason score. ROC analysis showed a decline in AUC with increasing biopsy Gleason score, from 0.64 for biopsy Gleason score 6, to 0.57 for Gleason score 7. ? In logistic regression models containing pretreatment variables, e.g. clinical stage and number of positive cores, for Gleason score 6 and 3 + 4, PSAD was the strongest predictor of subsequent tumour upgrade (odds ratio [OR] 1.46, 95% confidence interval [95% CI] 1.18-1.83, P = 0.001 and OR 1.37, 95% CI 1.14-1.67, P = 0.002, respectively). ? Surprisingly, in tumours upgraded from Gleason score 7 to > 7, PSAD was not predictive even on univariable analysis, whereas clinical stage and number of positive cores were significant independent predictors. To explore the relationship between serum PSA and Gleason score, tumour volume was calculated in 669 patients. ? There was a strong association between Gleason score and tumour volume, with the median volume of Gleason score 7 and Gleason score >7 tumours being approximately twice and four-times that of Gleason score 6 tumours, respectively (P < 0.001). ? In contrast, the median serum PSA level per millilitre tumour volume decreased significantly with increasing grade, from 5.4 ng/mL for Gleason score 6 to 2.1 ng/mL for > 7 (P < 0.001). CONCLUSIONS: ? There is a strong correlation between Gleason score and tumour volume in well/intermediate differentiated tumours, and as they produce relatively high amounts of PSA per unit volume of cancer, high PSAD is the strongest single predictor of tumour undergrading. ? However, as higher grade tumours produce less PSA per unit volume, PSAD loses its predictive ability, and other clinical markers of tumour volume such as palpable disease and numbers of positive cores become more predictive.
机译:目标:要分析PSA密度(PSAD)的性能,作为按Gleason评分分层的大型队列中Gleason评分提升的预测指标。 ?我们和其他人已表明,最初的前列腺活检和最终的根治性前列腺切除术(RP)病理之间的Gleason评分提高是局部治疗后复发的重要危险因素。患者与方法:从两个前瞻性数据库中识别出具有匹配的活检信息的RP患者。 ?根据活检和最终病理学Gleason评分之间的一致性对患者进行了分析,分为三对:6 /> 6、3 + 4 /> 3 + 4、7 /> 7。 ?通过格里森评分分层生成接收者操作特征(ROC)曲线,并计算曲线下面积(AUC)。 ?拟合逻辑回归模型以鉴定肿瘤升级的重要预测因子。结果:?在1516名患者中,有435名(29%)的格里森评分得到了提高。 ROC分析显示,随着活检格里森评分的升高,AUC下降,从活检格里森评分6的0.64降至格里森评分7的0.57。在包含预处理变量的逻辑回归模型中,例如对于格里森评分6和3 + 4,PSAD是随后肿瘤升级的最强预测指标(优势比[OR] 1.46、95%置信区间[95%CI] 1.18-1.83,P = 0.001),临床阶段和阳性核心数,PSAD是最强的预测和OR 1.37,95%CI 1.14-1.67,P = 0.002)。 ?出乎意料的是,在从格里森评分7升至> 7的肿瘤中,即使单因素分析也无法预测PSAD,而临床分期和阳性核心数是重要的独立预测因子。为了探讨血清PSA与Gleason评分之间的关​​系,计算了669例患者的肿瘤体积。 ?格里森评分与肿瘤体积之间有很强的相关性,格里森评分7和格里森评分> 7的中位体积分别约为格里森评分6肿瘤的两倍和四倍(P <0.001)。 ?相比之下,每毫升肿瘤体积的血清PSA中值随等级的升高而显着降低,从Gleason评分6的5.4 ng / mL降至> 7的2.1 ng / mL(P <0.001)。结论:?在良好/中度分化的肿瘤中,格里森评分与肿瘤体积之间有很强的相关性,并且由于它们每单位体积的癌症产生相对大量的PSA,因此高PSAD是肿瘤恶化的最强单一预测因子​​。 ?但是,随着更高级别的肿瘤每单位体积产生更少的PSA,PSAD失去了预测能力,而肿瘤体积的其他临床标志(例如可触及的疾病和阳性核心的数量)也变得更具预测性。

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