Evidence map›Paper›PMID 30291535›Full record

ArticleMedical oncology (Northwood, London, England)2018

Association of ERG/PTEN status with biochemical recurrence after radical prostatectomy for clinically localized prostate cancer.

Rohit Mehra, Simpa S Salami, Robert Lonigro, Ritu Bhalla, Javed Siddiqui, Xuhong Cao, Daniel E Spratt, Ganesh S Palapattu, Nallasivam Palanisamy, John T Wei and 2 more

Open access · greenAbstract read
In one paragraph

Article in Medical oncology (Northwood, London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 8% 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, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. The impact of PTEN deletion and ERG rearrangement on recurrence after treatment for prostate cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Pooled it
  3. Article
  4. Article
  5. Article
  6. Comedonecrosis Gleason pattern 5 is associated with worse clinical outcome in operated prostate cancer patients.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Precise Immunodetection of PTEN Protein in Human Neoplasia.Cold Spring Harbor perspectives in medicine · 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

12 authors at 6 institutions in 1 country.

Rohit MehraDepartment of Pathology, University of Michigan Health System, Ann Arbor, MI, USA. mrohit@med.umich.edu.ORCID http://orcid.org/0000-0002-6955-8884
Simpa S SalamiUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Robert LonigroMichigan Center for Translational Pathology, Ann Arbor, MI, USA.
Ritu BhallaLSU Health Sciences Center, New Orleans, MI, USA.
Javed SiddiquiMichigan Center for Translational Pathology, Ann Arbor, MI, USA.
Xuhong CaoMichigan Center for Translational Pathology, Ann Arbor, MI, USA.
Daniel E SprattUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Ganesh S PalapattuUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Nallasivam PalanisamyDepartment of Urology, Vattikuti Urology Institute, Henry Ford Health System, Detroit, MI, USA.
John T WeiDepartment of Urology, University of Michigan Health System, Ann Arbor, MI, USA.
Arul M ChinnaiyanDepartment of Pathology, University of Michigan Health System, Ann Arbor, MI, USA.
Scott A TomlinsDepartment of Pathology, University of Michigan Health System, Ann Arbor, MI, USA. tomlinss@umich.edu.
University of Michigan · USMichigan Center for Translational Pathology · USHenry Ford Health System · USHoward Hughes Medical Institute · USLouisiana State University Health Sciences Center New Orleans · USMichigan Medicine · US

Funding

Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Robert Timothy Dess · 2014 to 2026
$27.6M
Discovery and qualification of transcriptomic biomarkers for the early detection of aggressive prostate cancerU01CA214170 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 2016 to 2021
$3.3M
Howard Hughes Medical InstituteNational Institute of Health CA214170NCI NIH HHS P50 CA186786NCI NIH HHS U01 CA214170
6 · The paper itself

Abstract

We have previously demonstrated a significant correlative relationship between PTEN deletion and ERG rearrangement, both in the development of clinically localized prostate cancers and metastases. Herein, we evaluate the cooperative role of ERG and PTEN in oncological outcomes after radical prostatectomy for clinically localized prostate cancer. We evaluated ERG and PTEN status using three previously described cohorts. The first cohort included 235 clinically localized prostate cancer cases represented on tissue microarrays (TMA), evaluated using previously validated FISH assays for ERG and PTEN. The second cohort included 167 cases of clinically localized prostate cancer on TMAs evaluated for PTEN by FISH, and for PTEN and ERG by dual IHC. The third cohort comprised 59 clinically localized prostate cancer cases assessed by array comparative genomic hybridization (aCGH). Kaplan-Meir plots and long rank tests were used to assess the association of ERG and PTEN status with biochemical recurrence after radical prostatectomy for clinically localized prostate cancer. Of the 317 cases eligible for analyses with evaluable ERG and PTEN status, 88 (27.8%) patients developed biochemical recurrence over a median follow-up of 5.7 years. Overall, 45% (142/317) of cases demonstrated ERG rearrangement and 20% (62/317) of cases demonstrated PTEN loss. Hemizygous and homozygous deletion of PTEN was seen in 10% (18/175) and 3% (5/175) of ERG-negative cases, respectively. In contrast, hemizygous and homozygous deletion of PTEN was seen in 11% (15/142) and 17% (24/123) of ERG-positive cases, respectively. PTEN loss (heterozygous or homozygous) was significantly associated with shorter time to biochemical recurrence compared to no PTEN loss (p < 0.001). However, ERG rearrangement versus no rearrangement was not associated with time to PSA recurrence (p = 0.15). Patients who exhibited ERG rearrangement and loss of PTEN had no significant difference in time to recurrence compared to patients with wild-type ERG and loss of PTEN (p = 0.30). Our findings confirm a mutual cooperative role of ERG and PTEN in the pathogenesis of prostate cancer, particularly for homozygous PTEN deletion. ERG did not stratify outcome either alone or in combination with PTEN in this cohort.

Indexed as

AgedBiomarkers, TumorCohort StudiesFollow-Up StudiesHumansMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisProstatectomyProstatic NeoplasmsPTEN PhosphohydrolaseSurvival RateTranscriptional Regulator ERGBiomarkers, TumorERG protein, humanPTEN PhosphohydrolasePTEN protein, humanTranscriptional Regulator ERGERGFluorescent in situ hybridization (FISH)ImmunohistochemistryProstate cancerPTEN

Identifiers

PMID30291535
PMCPMC6601345
OpenAlexW2895347925

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.