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Tytuł pozycji:

Prostate cancer in 432 men aged <50 years in the prostate-specific antigen era: a new outlook.

Tytuł:
Prostate cancer in 432 men aged <50 years in the prostate-specific antigen era: a new outlook.
Autorzy:
Gielchinsky I; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.; St Vincent's Prostate Cancer Centre, Darlinghurst, NSW, Australia.
Chang J; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.; St Vincent's Prostate Cancer Centre, Darlinghurst, NSW, Australia.
Cusick T; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.
Delprado W; Douglass Hanly Moir Pathology, Macquarie Park, NSW, Australia.; School of Medicine, University of New South Wales, Kensington, NSW, Australia.
Nguyen Q; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.
Yuen C; School of Medicine, University of New South Wales, Kensington, NSW, Australia.; St Vincent's Clinic, Sydney, NSW, Australia.
Savdie R; School of Medicine, University of New South Wales, Kensington, NSW, Australia.; St Vincent's Clinic, Sydney, NSW, Australia.
Böhm M; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.
Haynes AM; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.
Scheltema MJ; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.; St Vincent's Prostate Cancer Centre, Darlinghurst, NSW, Australia.
Stricker PD; Garvan Institute of Medical Research, Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.; St Vincent's Prostate Cancer Centre, Darlinghurst, NSW, Australia.; School of Medicine, University of New South Wales, Kensington, NSW, Australia.; St Vincent's Clinic, Sydney, NSW, Australia.
Źródło:
BJU international [BJU Int] 2018 Nov; Vol. 122 Suppl 5, pp. 35-41. Date of Electronic Publication: 2018 Nov 08.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Oxford, UK : Blackwell Science, c1999-
MeSH Terms:
Prostatectomy*
Watchful Waiting*
Prostatic Neoplasms/*pathology
Prostatic Neoplasms/*therapy
Disease-Free Survival ; Follow-Up Studies ; Humans ; Kaplan-Meier Estimate ; Lymphatic Metastasis ; Male ; Middle Aged ; Neoplasm Staging ; Neoplasm, Residual ; Prostate-Specific Antigen/blood ; Prostatic Neoplasms/blood ; Retrospective Studies ; Risk Assessment/methods ; Treatment Outcome
Contributed Indexing:
Keywords: #PCSM; #ProstateCancer; #prostatejc; #uroonc; PSA era; prostate cancer; under 50
Substance Nomenclature:
EC 3.4.21.77 (Prostate-Specific Antigen)
Entry Date(s):
Date Created: 20181011 Date Completed: 20190819 Latest Revision: 20190819
Update Code:
20240104
DOI:
10.1111/bju.14586
PMID:
30303599
Czasopismo naukowe
Objective: To evaluate the clinical presentation and treatment outcomes of prostate cancer (PCa) in 432 consecutive patients aged < 50 years in the prostate-specific antigen (PSA) era.
Methods: Retrospective analysis was performed on all patients with PCa (14 570) from the years 1994 to 2017. A total of 432 consecutive patients aged < 50 years were identified. The patients were stratified by D'Amico risk groups, and their clinical presentation and treatment outcomes were analysed. The rates of biochemical recurrence after surgery were compared with the D'Amico prediction model as well as with older propensity-score-matched patients. The surgical pathology results in patients undergoing active surveillance (AS) were compared with those of low-risk patients who underwent immediate surgery.
Results: A total of 44%, 42% and 13% of patients harboured low-risk, intermediate-risk and high-risk PCa, respectively. Their median age was 47 years and a positive family history of PCa was reported in 39.1%. Clinical stage was T1 in 65.5% and T2 in 30.0% of patients, and 2.0% of patients had metastatic disease at presentation. Radical prostatectomy (RP) was performed in 78.4% of patients (n = 339) and the biochemical recurrence rates were 7.8% (low-risk), 15.3% (intermediate-risk) and 23.3% (high-risk) at 5 years post-surgery. These rates were lower than expected according to the D'Amico prediction model or when compared with older matched patients. A total of 74 patients with low-risk PCa underwent AS and only 17.6% (n = 13) required radical treatment after a median follow-up of 46 months. The surgical pathology results in patients undergoing ASdid not differ significantly from patients with low-risk PCa who underwent immediate surgery (positive surgical margins [P = 0.145], tumour volume [P = 0.257] or seminal vesicle involvement [P = 0.100]). Of the present cohort, only 0.4% died from PCa during a median follow-up of 65 months.
Conclusions: The clinical presentation and prognosis of young patients has changed dramatically during the PSA era. Patients nowadays present with lower-risk disease that can be treated adequately, with reassuring biochemical recurrence rates at 5 years post-surgery. AS appears to be safe in patients with low-risk. PCa.
(© 2018 The Authors BJU International © 2018 BJU International Published by John Wiley & Sons Ltd.)
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