期刊
CANCER MEDICINE
卷 10, 期 21, 页码 7772-7780出版社
WILEY
DOI: 10.1002/cam4.4274
关键词
Gleason score; prostate biopsy; prostate cancer; radical prostatectomy
类别
资金
- Tianjin science and technology plan project [19ZXDBSY00050]
- Science and Technology Project of Tianjin Health Committee [ZC20116]
This study investigated the risk factors of Gleason score upgrading (GSU) after radical prostatectomy (RP) in a Chinese cohort. The results showed that clinical stage >= T2c, the number of positive cores <3, and lower positive rate of biopsy were identified as risk factors of GSU. This information may guide clinicians in accurately judging the biopsy pathological grading and formulating treatment strategies.
Background To study the risk factors of Gleason score upgrading (GSU) after radical prostatectomy (RP) in a Chinese cohort. Methods The data of 637 patients who underwent prostate biopsy and RP in our hospital from January 2014 to January 2021 were retrospectively analyzed. The age, body mass index (BMI), prostate-specific antigen (PSA) level, testosterone (TT) level, neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), eosinophil-to-lymphocyte ratio (ELR), aspartate aminotransferase/alanine transaminase (AST/ALT) ratio, clinical stage, the biopsy method, and pathological characteristics of specimens after biopsy and RP were collected for all patients. Univariate analysis and multivariate logistic regression analysis were used to analyze the risk factors of GSU after RP. The predictive efficacy was verified with the area under the curve (AUC) of the receiver operating characteristic (ROC) curve. We performed the analysis separately in the overall cohort and in the cohort with Gleason score (GS) = 6. Results In the overall cohort, 177 patients (27.79%) had GSU, and in the GS = 6 cohort, 68 patients (60.18%) had GSU. Multivariate logistic regression analysis showed that in the overall cohort, clinical stage >= T2c (OR = 3.201, p < 0.001), the number of positive cores >= 3 (OR = 0.435, p = 0.04), and positive rate of biopsy (OR = 0.990, p = 0.016) can affect whether GS is upgraded, and the AUC of the combination of the three indicators for predicting the occurrence of GSU was 0.627. In the GS = 6 cohort, multivariate logistic regression analysis showed that clinical stage >= T2c (OR = 4.690, p = 0.001) was a risk factor for GSU, and the AUC predicted to occur GSU is 0.675. Conclusion Clinical stage >= T2c, the number of positive cores <3, and lower positive rate of biopsy are the risk factors of GSU. This study may provide some references for clinicians to judge the accuracy of biopsy pathological grading and formulate treatment strategies, but the specific effect still needs clinical practice certification.
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