S2,3PSA% as a predictor of reclassification of 1st protocol biopsy on active surveillance for early-stage prostate cancer patients: From the PRIAS-JAPAN study.
Abstract
358 Background: Recently, α2,3-sialylated prostate-specific antigen (S2,3PSA)% has been developed as a new serum biomarker for Prostate cancer (PCa). So, we aimed to investigate S2,3 PSA% to predict reclassification of the first repeat protocol biopsy (1st re-PBx) on Active surveillance (AS) for PCa patients. Methods: Patients who participated in PRIAS-JAPAN and its ancillary studies from August 2013 to January 2022 and met the following criteria were included: clinical stage: T1c/T2, PSA: <10ng/ml, PSA density: <0.2ng/ml/cc, number of positive cores: <2, Gleason score: <6. All participants were required to receive a blood sampling test on a protocol visit at inclusion and at the 1st re-PBx. Significant predictors of reclassification in 1st re-PBx were investigated in univariate and multivariate analyses by logistic regression analysis. Then, to assess the predictive power and thresholds for reclassification, we plotted Receiver Operating Characteristic (ROC) curves. Further, a decision curve analysis (DCA) was conducted to identify net benefits. Results: A total of 188 patients were analyzed. Reclassification was shown in 61 patients (32.4%). Both univariate and multivariate analysis by logistic regression analysis showed that S2,3PSA% at diagnosis and before 1st re-biopsy were both significant predictors of reclassification. In ROC analysis, S2,3 PSA% at diagnosis and before 1st re-biopsy had comparable predictive power. The AUC for S2,3PSA% before 1st re-biopsy was 0.63, with a sensitivity of 0.41 and specificity of 0.87. Analysis of the net benefit of PSA doubling time (PSADT) and S2,3PSA% with DCA using PSA, prostate volume, and age as the base model showed that S2,3PSA% had a higher net benefit than PSADT. Conclusions: S2,3PSA% before 1st re-PBx has a high net benefit for reclassification and is a useful tool for clinical decision making. Result of ROC curve analysis and decision curve analysis about S2,3PSA% for reclassification at 1st repeat biopsy. ROC curves about reclassification for differences in S2,3PSA% between baseline and before the 1st repeat PBx Variable AUC Standard Error p value (for AUC) 95% CI Optimal cut off point Sensitivity Specificity p value (vs baseline) S2,3PSA%(baseline) 0.65 0.05 <0.001 0.56 - 0.74 44.3 54.1% 75.6% - S2,3PSA%(before 1yr PBx) 0.63 0.05 0.0065 0.54 - 0.72 1.64 41.0% 87.4% 0.33 Decision curve analysis for reclassification at 1st repeat biopsy High Risk Threshold 0 0.1 0.2 0.3 0.4 0.5 Baseline model* 1 0.769 0.488 0.222 0.044 -0.016 Baseline model+PSADT** 1 0.77 0.492 0.29 0.011 -0.016 Baseline model+S2, 3PSA%** 1 0.769 0.504 0.215 0.186 0.131 *Baseline model is composed of age, prostate volume and PSA before 1yr PBx. **The value of PSADT and S2,3PSA% are calculated by the data before 1yr PBx.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (14)
Takuma Kato
Tohru Yoneyama
Hirosaki University Graduate School of Medicine, Hirosaki, Japan
Shingo Hatakeyama
Yoichiro Tohi
Kagawa University, Kita-Gun, Japan
Ryuji Matsumoto
Hokkaido University, Sapporo-Shi, Japan
Takuma Sato
Katsuyoshi Hashine
Takahiro Kimura
Toshiki Tanikawa
Niigata Cancer Center Hospital, Niigata, Japan
Takayuki Goto
Masaharu Inoue
Saitama Cancer Center, Saitama, Japan
Kohei Hashimoto
Chikara Ohyama
Mikio Sugimoto
Kagawa University, Kagawa, Japan