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  4. Outcomes of prostate atypical small acinar proliferation and high-grade prostate intraepithelial neoplasm patients
 
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Outcomes of prostate atypical small acinar proliferation and high-grade prostate intraepithelial neoplasm patients

Journal
Urological Science
Journal Volume
29
Journal Issue
3
Pages
161-165
Date Issued
2018
Author(s)
Tung S.-Y.
YEONG-SHIAU PU  
CHAO-YUAN HUANG  
HONG-CHIANG CHANG  
KUO-HOW HUANG  
SHUO-MENG WANG  
Tai H.-C.
CHUNG-HSIN CHEN  
DOI
10.4103/UROS.UROS_52_18
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049501960&doi=10.4103%2fUROS.UROS_52_18&partnerID=40&md5=e14eba3e36ed44bec185bab979dfc115
https://scholars.lib.ntu.edu.tw/handle/123456789/541933
Abstract
Objective: Atypical small acinar proliferation (ASAP) and high-grade prostatic intraepithelial neoplasia (HGPIN) are two pathological findings occasionally noted in prostate biopsies. Previous Western studies reported that they were associated with prostate cancer. However, none Taiwanese series report the subsequent cancer detection in ASAP and HGPIN patients. This study aimed to examine the results of repeated biopsies in the patients with ASAP and HGPIN. Materials and Methods: A total of 220 consecutive patients with ASAP and/or HGPIN at our institute between January 1990 and December 2010 were enrolled. Patient demographics and clinical information were extracted from the electronic database of our institute. Prostate biopsies were performed through transrectal ultrasound guidance. The patients who had concurrent prostate cancer (n = 51) and no repeated prostate biopsies (n = 103) were excluded from the study. Patients with biopsy pathologies reporting low-grade prostatic intraepithelial neoplasia (n = 2) were also excluded. The remaining 64 patients were available for the final analysis. Results: Nearly, 38, 24, and 2 patients were initially diagnosed as ASAP, HGPIN, and ASAP along with HGPIN, respectively. After 10 years of follow-up, 36.8% patients in ASAP group developed prostate cancer, while 16.7% in HGPIN group and 100% in ASAP + HGPIN group. Median time to developing prostate cancer were 20 months in ASAP group, 31 months in HGPIN group, and 48 months in ASAP + HGPIN group. There was no significant difference of prostate cancer development between ASAP and HGPIN group (P = 0.291). Only older age, classified by 65 years, was significantly associated with a higher detection rate of prostate cancer. Conclusion: Patients with the initial diagnosis of ASAP or PIN has a high risk of developing prostate cancer. Therefore, those patients should be well announced and followed regularly. ? 2018 Medknow Publications. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
adult; aged; Article; atypical small acinar proliferation; cancer diagnosis; cancer grading; cancer patient; cancer risk; clinical decision making; clinical protocol; cohort analysis; controlled study; demography; disease association; disease course; follow up; human; human tissue; major clinical study; male; outcome assessment; physician; priority journal; prostate biopsy; prostate cancer; prostatic intraepithelial neoplasia; senescence; transrectal ultrasonography; tumor biopsy
Publisher
Wolters Kluwer Medknow Publications
Type
journal article

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To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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