Combining CAPRA-S With Tumor IDC/C Features Improves the Prognostication of Biochemical Recurrence in Prostate Cancer Patients

被引:4
作者
Jeyapala, Renu [1 ,2 ]
Kamdar, Shivani [1 ,3 ]
Olkhov-Mitsel, Ekaterina [1 ,3 ]
Zlotta, Alexandre [4 ,5 ]
Fleshner, Neil [4 ,5 ]
Visakorpi, Tapio [6 ,7 ,8 ,9 ]
van der Kwast, Theodorus [3 ]
Bapat, Bharati [1 ,2 ,3 ,4 ,5 ]
机构
[1] Sinai Hlth Syst, Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[3] Univ Toronto Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] Univ Hlth Network Toronto, Dept Surg, Div Urol, Toronto, ON, Canada
[5] Univ Hlth Network Toronto, Dept Surg Oncol, Div Urol, Toronto, ON, Canada
[6] Tampere Univ, Fac Med & Hlth Technol, Tampere, Finland
[7] Tampere Univ Hosp, Tays Ctr, Tampere, Finland
[8] Tampere Univ Hosp, Fimlab Labs Ltd, Tampere, Finland
[9] Univ Hlth Network, Dept Pathol & Lab Med, Toronto, ON, Canada
关键词
prostate cancer; Biochemical Recurrence; nomograms; intraductal carcinoma; Cribiform architecture; ISUP CONSENSUS-CONFERENCE; INTRADUCTAL CARCINOMA; RADICAL-PROSTATECTOMY; RISK STRATIFICATION; CRIBRIFORM; PREDICTION; HETEROGENEITY; DEFINITION; DIAGNOSIS; DISEASE;
D O I
10.1016/j.clgc.2022.01.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biomarker panels must remain significantly associated with the outcomes across patient cohorts and add to pre-existing nomograms. We validated the prognostic ability of both IDC/C and CAPRA-S for BCR and time to BCR in over 600 patients (3 cohorts). CAPRA-S and IDC/C was significant in recurrence-free survival and an independent predictor of BCR. Background: Intraductal carcinoma and cribriform (IDC/C) tumor features are well-established prognosticators of biochemical recurrence (BCR), metastasis, and prostate cancer (PCa)-specific mortality. However, approximately 70% of PCa patients undergoing a radical prostatectomy are IDC/C negative, yet up-to 20% of these patients progress and experience BCR. Thus, tumor histopathologic characteristics such as IDC/C alone are limited in their ability to predict disease progression. Conversely, several nomograms such as Cancer of the Prostate Risk Assessment-Surgery (CAPRA-S) have been developed to aid in the prognostication of BCR, but not yet widely applied in clinical settings. Materials and methods: In this study, we assessed the combined prognostic utility of IDC/C, and CAPRA-S for BCR in 3 PCa patient cohorts. Results: CAPRA-S+IDC/C improved the predictive accuracy of BCR in all 3 cohorts (P <:.001). Specifically, among IDC/C negative cases, CAPRA-S improved the prognostication of BCR in low-risk (Cohort 1; P < .001, Cohort 2; P < .001, Cohort 3; P = .003), intermediate (Cohort 1; P < .001, Cohort 2; P = .006, Cohort 3; P = .03) and high-risk (Cohort 1-3; P < .001) patients. Conversely, IDC/C improved the prognostication of BCR among CAPRAS low-risk (Cohorts 1; P < .001 and Cohort 3; P = .003) patients. Conclusion: Our results suggest the investigation of histopathological IDC/C features in CAPRA-S low-risk patients and conversely, nomogram CAPRA-S among IDC/C negative patients improves the identification of patients likely to experience BCR, which would otherwise be missed through current assessment regimens. These patients can be offered more intensive monitoring and adjuvant therapies upfront to circumvent the development of recurrent cancer or overtreatment at the time of surgery. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:E217 / E226
页数:10
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