Advertisement
Original Study| Volume 15, ISSUE 6, e1117-e1122, December 2017

Favorable Gleason 3 + 4 Prostate Cancer Shows Comparable Outcomes With Gleason 3 + 3 Prostate Cancer: Implications for the Expansion of Selection Criteria for Active Surveillance

Published:August 02, 2017DOI:https://doi.org/10.1016/j.clgc.2017.07.020

      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 access
      One-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 Cancer
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Klotz L.
        • Vesprini D.
        • Sethukavalan P.
        • et al.
        Long-term follow-up of a large active surveillance cohort of patients with prostate cancer.
        J Clin Oncol. 2015; 33: 272-277
        • Dall'Era M.A.
        • Klotz L.
        Active surveillance for intermediate-risk prostate cancer.
        Prostate Cancer Prostatic Dis. 2017; 20: 1-6
        • National Comprehensive Cancer Network
        Clinical practice guidelines in oncology. Prostate cancer, version 1. 2017.
        (Available at:) (Accessed: August 3, 2017)
        • Cooperberg M.R.
        • Cowan J.E.
        • Hilton J.F.
        • et al.
        Outcomes of active surveillance for men with intermediate-risk prostate cancer.
        J Clin Oncol. 2011; 29: 228-234
        • Bul M.
        • van den Bergh R.C.
        • Zhu X.
        • et al.
        Outcomes of initially expectantly managed patients with low or intermediate risk screen-detected localized prostate cancer.
        BJU Int. 2012; 110: 1672-1677
        • Newcomb L.F.
        • Thompson Jr., I.M.
        • Boyer H.D.
        • et al.
        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
        • Selvadurai E.D.
        • Singhera M.
        • Thomas K.
        • et al.
        Medium-term outcomes of active surveillance for localized prostate cancer.
        Eur Urol. 2013; 64: 981-987
        • Epstein J.I.
        • Allsbrook W.C.
        • Amin M.B.
        • Egevad L.L.
        • ISUP Grading Committee
        The 2005 International Society of Urological Pathology (ISUP) Consensus Conference on Gleason Grading of Prostatic Carcinoma.
        Am J Surg Pathol. 2005; 29: 1228-1242
        • Gandaglia G.
        • Schiffmann J.
        • Schlomm T.
        • et al.
        Identification of pathologically favorable disease in intermediate-risk prostate cancer patients: implications for active surveillance candidates selection.
        Prostate. 2015; 75: 1484-1491
        • Raldow A.C.
        • Zhang D.
        • Chen M.H.
        • Braccioforte M.H.
        • Moran B.J.
        • D'Amico A.V.
        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
        • Lee H.
        • Kuk H.
        • Byun S.S.
        • Lee S.E.
        • Hong S.K.
        Preoperative glycemic control status as a significant predictor of biochemical recurrence in prostate cancer patients after radical prostatectomy.
        PLoS One. 2015; 10: e0124761
        • Morlacco A.
        • Cheville J.C.
        • Rangel L.J.
        • Gearman D.J.
        • Jeffrey Karnes R.
        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
        • Stephenson A.J.
        • Kattan M.W.
        • Eastham J.A.
        • et al.
        Prostate cancer–specific mortality after radical prostatectomy for patients treated in the prostate-specific antigen era.
        J Clin Oncol. 2009; 27: 4300-4305
        • Stattin P.
        • Holmberg E.
        • Johansson J.E.
        • et al.
        Outcomes in localized prostate cancer: National Prostate Cancer Register of Sweden follow-up study.
        J Natl Cancer Inst. 2010; 102: 950-958
        • Wright J.L.
        • Salinas C.A.
        • Lin D.W.
        • et al.
        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
        • D'Amico A.V.
        • Whittington R.
        • Malkowicz S.B.
        • et al.
        Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer.
        JAMA. 1998; 280: 969-974
        • Ploussard G.
        • Isbarn H.
        • Briganti A.
        • et al.
        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
        • Wong L.M.
        • Tang V.
        • Peters J.
        • Costello A.
        • Corcoran N.
        Feasibility for active surveillance in biopsy Gleason 3 + 4 prostate cancer: an Australian radical prostatectomy cohort.
        BJU Int. 2016; 117: 82-87
        • Bokhorst L.P.
        • Valdagni R.
        • Rannikko A.
        • et al.
        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
        • Faisal F.A.
        • Sundi D.
        • Pierorazio P.M.
        • et al.
        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
        • Dinh K.T.
        • Muralidhar V.
        • Mahal B.A.
        • et al.
        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
        • Huang C.C.
        • Kong M.X.
        • Zhou M.
        • et al.
        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
        • Perlis N.
        • Sayyid R.
        • Evans A.
        • et al.
        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
        • Epstein J.I.
        • Egevad L.
        • Amin M.B.
        • et al.
        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
        • Cuzick J.
        • Stone S.
        • Fisher G.
        • et al.
        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
        • Cullen J.
        • Rosner I.L.
        • Brand T.C.
        • et al.
        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
        • Kearns J.T.
        • Lapin B.
        • Wang E.
        • et al.
        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
        • de Cobelli O.
        • Terracciano D.
        • Tagliabue E.
        • et al.
        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
        • Chung M.S.
        • Lee S.H.
        Current status of active surveillance in prostate cancer.
        Investig Clin Urol. 2016; 57: 14-20