Evidence map›Paper›PMID 26857145›Full record

ReviewProstate cancer and prostatic diseases2016

Atypical small acinar proliferation (ASAP): Is a repeat biopsy necessary ASAP? A multi-institutional review.

A Leone, B Gershman, K Rotker, C Butler, J Fantasia, A Miller, A Afiadata, A Amin, A Zhou, Z Jiang and 8 more

Abstract readMulticenter StudyReview
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In one paragraph

Review in Prostate cancer and prostatic diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

A LeoneDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
B GershmanDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
K RotkerDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
C ButlerDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
J FantasiaDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
A MillerDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
A AfiadataDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
A AminDepartment of Pathology and Laboratory Medicine, Rhode Island Hospital, Providence, RI, USA.
A ZhouDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
Z JiangDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
T SeboDepartment of Pathology, Mayo Clinic, Rochester, MN, USA.
A MegaDepartment of Hematology/Oncology, The Miriam Hospital, Providence, RI, USA.
S SchiffDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
G PareekDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
D GolijaninDivision of Urology, Rhode Island Hospital, Providence, RI, USA.
J YatesDepartment of Urology, University of Massachusetts Medical School, Worcester, MA, USA.
R J KarnesDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
J RenzulliDivision of Urology, Rhode Island Hospital, Providence, RI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtypical small acinar proliferation (ASAP) occurs in approximately 5% of prostate biopsies. Approximately 30-40% of patients with ASAP may develop prostate cancer (PCa) within a 5-year period. Current guidelines recommend a repeat biopsy within 3-6 months after the initial diagnosis. Our objective was to examine the association between ASAP and subsequent diagnosis of high-grade PCa and to evaluate the need for immediate repeat biopsy.

methodsA retrospective multi-institutional review identified 264 patients who underwent prostate biopsy from 2000 to 2013 (Brown), 2008 to 2013 (University of Massachusetts) and 1994 to 2005 (Mayo) and were diagnosed with ASAP. Patients underwent transrectal ultrasound-guided biopsies for elevated PSA and/or abnormal digital rectal exam. Clinicopathologic features were assessed, including rates of subsequent PCa detection of any high-grade (Gleason 7-10) PCa. Comparison was made between those with subsequent PCa on repeat biopsy and those with benign repeat pathology.

resultsAll 264 patients included underwent repeat biopsy with a median follow-up of 5.4 years (interquartile range: 4.6, 6.7). Of these patients, 89 (34%) were subsequently diagnosed with PCa including 21 (8%) with high-grade PCa. Pre-biopsy PSA was higher among patients subsequently diagnosed with (6.7 vs 5.8, P<0.001). Of those diagnosed with subsequent PCa, 69/89 (78%) had less than or equal to Gleason 3+3 disease and only 15/89 (17%) had Gleason 7 and 6/89 (6%) revealed Gleason ⩾8-10. Radical prostatectomy was performed on 36/89 (40%) patients. Surgical pathology revealed 11 patients ⩾Gleason 8-10 PCa.

conclusionsAlthough 34% of patients with an initial diagnosis of ASAP who had repeat biopsy were subsequently diagnosed with PCa only, only 22% (8% of the total cohort) were found to have high-grade disease. Higher PSA was associated with increased risk of identifying PCa on repeat biopsy. These findings suggest that immediate repeat biopsy may be omitted in the majority of men with ASAP.

Indexed as

Cell ProliferationAcinar CellsAgedBiopsy, NeedleHumansMaleMiddle AgedNeoplasm GradingProstateProstatectomyProstate-Specific AntigenProstatic NeoplasmsRetrospective StudiesProstate-Specific Antigen

Identifiers

PMID26857145

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.