Evidence map›Paper›PMID 30279579›Full record

ArticleProstate cancer and prostatic diseases2019

PTEN status assessment in the Johns Hopkins active surveillance cohort.

Jeffrey J Tosoian, Liana B Guedes, Carlos L Morais, Mufaddal Mamawala, Ashley E Ross, Angelo M De Marzo, Bruce J Trock, Misop Han, H Ballentine Carter, Tamara L Lotan

Abstract read
In one paragraph

Article in Prostate cancer and prostatic diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Subclonal Complete Loss of CDKN1B as a Common Genomic Alteration in Prostate Cancer: Associations With Race and Prostate Cancer Outcomes.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2026
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  10. [Active surveillance in prostate cancer].Der Urologe. Ausg. A · 2019
    Review
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

10 authors at 2 institutions in 1 country.

Jeffrey J TosoianDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Liana B GuedesDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Carlos L MoraisDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Mufaddal MamawalaDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Ashley E RossDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Angelo M De MarzoDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Bruce J TrockDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Misop HanDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
H Ballentine CarterDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Tamara L LotanDepartment of Urology, Johns Hopkins School of Medicine, Baltimore, MD, USA. tlotan1@jhmi.edu.
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA015704
6 · The paper itself

Abstract

backgroundUp to half of men with Gleason score 6 (GS6) prostate cancers initially managed with active surveillance (AS) will eventually require definitive therapy, usually due to tumor grade reclassification during follow-up. We examined the association between PTEN status on biopsy and subsequent clinicopathologic outcomes in men with GS6 cancers who enrolled in AS.

methodsWe performed a case-control study of men enrolled in the Johns Hopkins AS cohort with diagnostic biopsy tissue available for immunohistochemical (IHC) staining. IHC was performed for PTEN using genetically validated protocols for all patients. Cases included men who underwent grade reclassification to GS ≥ 3 + 4 = 7 on biopsy within 2 years of follow-up (i.e., early reclassification) or reclassification to GS ≥ 4 + 3 = 7 on biopsy or radical prostatectomy during follow-up (i.e., extreme reclassification). Control patients were diagnosed with GS6 cancer and monitored on AS for at least 8 years without undergoing biopsy reclassification.

resultsAmong 67 cases with adequate tissue, 31 men underwent early reclassification and 36 men underwent extreme reclassification. Cases were compared to 65 control patients with adequate tissue for assessment. On initial prostate biopsy, cases were older (median age 67 vs. 65, p = 0.024) and were less likely to meet very-low-risk criteria (64 vs 79%, p = 0.042) as compared to controls. Although not statistically significant, PTEN loss was observed in only 1 (1.5%) of 65 controls as compared to 6 (9%) of 67 cases (p = 0.062).

conclusionsPTEN loss was rare among men with GS6 prostate cancer enrolled in AS at Johns Hopkins. Despite this, PTEN loss was more frequent among men who underwent early or extreme reclassification to higher-grade cancer as compared to controls. Additional studies in larger low-risk cohorts may better elucidate a potential role for PTEN in selecting patients for AS.

Indexed as

AgedBiomarkersBiopsyCase-Control StudiesDisease ManagementHealth Care SurveysHumansImmunohistochemistryMaleMiddle AgedNeoplasm GradingNeoplasm StagingProstatic NeoplasmsPTEN PhosphohydrolaseBiomarkersPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID30279579
PMCPMC6372343
OpenAlexW2895062358

What OpenQuestion holds

Textmetadata
LicenceTDM
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Registered trials

None linked

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.