Abstract
Background
To investigate the feasibility of active surveillance (AS) in biopsy Gleason score
(GS) 3 + 4 prostate cancer (PCa), we compared the outcomes of biopsy GS 3 + 3 and
3 + 4 PCa after radical prostatectomy.
Patients and Methods
We analyzed the data of 1491 patients undergoing radical prostatectomy for biopsy
GS 3 + 3 or 3 + 4 PCa who fulfilled the low-risk criteria of the National Comprehensive
Cancer Network guidelines regardless of GS. The favorable GS 3 + 4 group was defined
as having core involvement ≤ 50%, prostate-specific antigen density ≤ 0.2 ng/mL/cm3, and number of positive cores ≤ 2 (maximal 1 core of GS 3 + 4).
Results
The GS 3 + 4 group showed significantly worse pathologic outcomes, including pathologic
GS, pathologic stage, and seminal vesicle invasion rate (all P < .001), as well as worse biochemical recurrence–free survival (P < .001) than the GS 3 + 3 group. However, the favorable GS 3 + 4 subgroup showed
no significant differences in the pathologic outcomes (all P > .05) and in biochemical recurrence–free survival (P = .817) compared to the GS 3 + 3 group.
Conclusion
Despite the application of low-risk criteria, GS 3 + 4 PCa patients showed significantly
worse outcomes than GS 3 + 3 patients. However, favorable GS 3 + 4 patients showed
comparable clinicopathologic outcomes with GS 3 + 3 patients, suggesting possible
expansion of AS for the favorable GS 3 + 4 group.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Clinical Genitourinary CancerAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Long-term follow-up of a large active surveillance cohort of patients with prostate cancer.J Clin Oncol. 2015; 33: 272-277
- Active surveillance for intermediate-risk prostate cancer.Prostate Cancer Prostatic Dis. 2017; 20: 1-6
- Clinical practice guidelines in oncology. Prostate cancer, version 1. 2017.(Available at:) (Accessed: August 3, 2017)
- Outcomes of active surveillance for men with intermediate-risk prostate cancer.J Clin Oncol. 2011; 29: 228-234
- Outcomes of initially expectantly managed patients with low or intermediate risk screen-detected localized prostate cancer.BJU Int. 2012; 110: 1672-1677
- Outcomes of active surveillance for the management of clinically localized prostate cancer in the prospective, multi-institutional Canary PASS cohort.J Urol. 2015; 195: 313-320
- Medium-term outcomes of active surveillance for localized prostate cancer.Eur Urol. 2013; 64: 981-987
- The 2005 International Society of Urological Pathology (ISUP) Consensus Conference on Gleason Grading of Prostatic Carcinoma.Am J Surg Pathol. 2005; 29: 1228-1242
- Identification of pathologically favorable disease in intermediate-risk prostate cancer patients: implications for active surveillance candidates selection.Prostate. 2015; 75: 1484-1491
- Risk group and death from prostate cancer: implications for active surveillance in men with favorable intermediate-risk prostate cancer.JAMA Oncol. 2015; 1: 334-340
- Preoperative glycemic control status as a significant predictor of biochemical recurrence in prostate cancer patients after radical prostatectomy.PLoS One. 2015; 10: e0124761
- Adverse disease features in Gleason score 3 + 4 “favorable intermediate-risk” prostate cancer: implications for active surveillance.Eur Urol. 2017; 72 ([e-pub ahead of print]): 442-447
- Prostate cancer–specific mortality after radical prostatectomy for patients treated in the prostate-specific antigen era.J Clin Oncol. 2009; 27: 4300-4305
- Outcomes in localized prostate cancer: National Prostate Cancer Register of Sweden follow-up study.J Natl Cancer Inst. 2010; 102: 950-958
- Prostate cancer specific mortality and Gleason 7 disease differences in prostate cancer outcomes between cases with Gleason 4 + 3 and Gleason 3 + 4 tumors in a population based cohort.J Urol. 2009; 182: 2702-2707
- Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer.JAMA. 1998; 280: 969-974
- Can we expand active surveillance criteria to include biopsy Gleason 3 + 4 prostate cancer? A multi-institutional study of 2,323 patients.Urol Oncol. 2015; 33: 71.e1-71.e9
- Feasibility for active surveillance in biopsy Gleason 3 + 4 prostate cancer: an Australian radical prostatectomy cohort.BJU Int. 2016; 117: 82-87
- A decade of active surveillance in the PRIAS study: an update and evaluation of the criteria used to recommend a switch to active treatment.Eur Urol. 2016; 70: 954-960
- Outcomes of men with an elevated prostate-specific antigen (PSA) level as their sole preoperative intermediate- or high-risk feature.BJU Int. 2014; 114: E120-E129
- Occult high-risk disease in clinically low-risk prostate cancer with ≥50% positive biopsy cores: should national guidelines stop calling them low risk?.Urology. 2016; 87: 125-132
- Gleason score 3 + 4 = 7 prostate cancer with minimal quantity of Gleason pattern 4 on needle biopsy is associated with low-risk tumor in radical prostatectomy specimen.Am J Surg Pathol. 2014; 38: 1096-1101
- Limitations in predicting organ confined prostate cancer in patients with Gleason pattern 4 on biopsy: implications for active surveillance.J Urol. 2017; 197: 75-83
- The 2014 International Society of Urological Pathology (ISUP) Consensus Conference on Gleason Grading of Prostatic Carcinoma: Definition of Grading Patterns and Proposal for a New Grading System.Am J Surg Pathol. 2016; 40: 244-252
- Validation of an RNA cell cycle progression score for predicting death from prostate cancer in a conservatively managed needle biopsy cohort.Br J Cancer. 2015; 113: 382-389
- A biopsy-based 17-gene genomic prostate score predicts recurrence after radical prostatectomy and adverse surgical pathology in a racially diverse population of men with clinically low- and intermediate-risk prostate cancer.Eur Urol. 2015; 68: 123-131
- Associations between iCOGS single nucleotide polymorphisms and upgrading in both surgical and active surveillance cohorts of men with prostate cancer.Eur Urol. 2016; 69: 223-228
- Predicting pathological features at radical prostatectomy in patients with prostate cancer eligible for active surveillance by multiparametric magnetic resonance imaging.PLoS One. 2015; 10: e0139696
- Current status of active surveillance in prostate cancer.Investig Clin Urol. 2016; 57: 14-20
Article info
Publication history
Published online: August 02, 2017
Accepted:
July 27,
2017
Received in revised form:
July 24,
2017
Received:
April 10,
2017
Identification
Copyright
© 2017 Elsevier Inc. All rights reserved.