Evidence map›Paper›PMID 32914029›Full record

ArticleJCO precision oncology2019

Biologic Significance of Magnetic Resonance Imaging Invisibility in Localized Prostate Cancer.

Simpa S Salami, Jeremy B Kaplan, Srinivas Nallandhighal, Mandeep Takhar, Jeffrey J Tosoian, Matthew Lee, Junhee Yoon, Daniel H Hovelson, Komal R Plouffe, Samuel D Kaffenberger and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in JCO precision oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. The Precision Prostatectomy: an IDEAL Stage 0, 1 and 2a Study.BMJ surgery, interventions, & health technologies · 2019
    Article
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

24 authors at 6 institutions in 2 countries.

Simpa S SalamiMichigan Medicine, Ann Arbor, MI.
Jeremy B KaplanMichigan Medicine, Ann Arbor, MI.
Srinivas NallandhighalMichigan Medicine, Ann Arbor, MI.
Mandeep TakharGenomeDx Biosciences, San Diego, CA.
Jeffrey J TosoianMichigan Medicine, Ann Arbor, MI.
Matthew LeeMichigan Medicine, Ann Arbor, MI.
Junhee YoonCedars-Sinai Medical Center, Los Angeles, CA.
Daniel H HovelsonMichigan Medicine, Ann Arbor, MI.
Komal R PlouffeMichigan Medicine, Ann Arbor, MI.
Samuel D KaffenbergerMichigan Medicine, Ann Arbor, MI.
Edward M SchaefferNorthwestern University Feinberg School of Medicine, Chicago, IL.
R Jeffrey KarnesMayo Clinic, Rochester, MN.
Tamara L LotanJohns Hopkins Medical Institute, Baltimore, MD.
Todd M MorganMichigan Medicine, Ann Arbor, MI.
Arvin K GeorgeMichigan Medicine, Ann Arbor, MI.
Jeffrey S MontgomeryMichigan Medicine, Ann Arbor, MI.
Matthew S DavenportMichigan Medicine, Ann Arbor, MI.
Sungyong YouCedars-Sinai Medical Center, Los Angeles, CA.
Scott A TomlinsMichigan Medicine, Ann Arbor, MI.
Nicole E CurciMichigan Medicine, Ann Arbor, MI.
Hyung L KimCedars-Sinai Medical Center, Los Angeles, CA.
Daniel E SprattUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI.
Aaron M UdagerMichigan Medicine, Ann Arbor, MI.
Ganesh S PalapattuMichigan Medicine, Ann Arbor, MI.
Michigan Medicine · USUniversity of Michigan–Ann Arbor · USCedars-Sinai Medical Center · USJohns Hopkins Medicine · USMayo Clinic in Arizona · USNorthwestern University · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
Exploiting drivers of androgen receptor signaling negative prostate cancer for prR01CA183857 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TOMLINS, SCOTT A · 2014 to 2018
$1.6M
NCI NIH HHS P30 CA046592NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA183857
6 · The paper itself

Abstract

purposeMultiparametric magnetic resonance imaging (mpMRI) is used widely for prostate cancer (PCa) evaluation. Approximately 35% of aggressive tumors, however, are not visible on mpMRI. We sought to identify the molecular alterations associated with mpMRI-invisible tumors and determine whether mpMRI visibility is associated with PCa prognosis.

methodsDiscovery and validation cohorts included patients who underwent mpMRI before radical prostatectomy and were found to harbor both mpMRI-visible (Prostate Imaging and Reporting Data System 3 to 5) and -invisible (Prostate Imaging and Reporting Data System 1 or 2) foci on surgical pathology. Next-generation sequencing was performed to determine differential gene expression between mpMRI-visible and -invisible foci. A genetic signature for tumor mpMRI visibility was derived in the discovery cohort and assessed in an independent validation cohort. Its association with long-term oncologic outcomes was evaluated in a separate testing cohort.

resultsThe discovery cohort included 10 patients with 26 distinct PCa foci on surgical pathology, of which 12 (46%) were visible and 14 (54%) were invisible on preoperative mpMRI. Next-generation sequencing detected prioritized genetic mutations in 14 (54%) tumor foci (n = 8 mpMRI visible, n = 6 mpMRI invisible). A nine-gene signature (composed largely of cell organization/structure genes) associated with mpMRI visibility was derived (area under the curve = 0.89), and the signature predicted MRI visibility with 75% sensitivity and 100% specificity (area under the curve = 0.88) in the validation cohort. In the testing cohort (n = 375, median follow-up 8 years) there was no significant difference in biochemical recurrence, distant metastasis, or cancer-specific mortality in patients with predicted mpMRI-visible versus -invisible tumors (all

conclusionCompared with mpMRI-invisible disease, mpMRI-visible tumors are associated with underexpression of cellular organization genes. mpMRI visibility does not seem to be predictive of long-term cancer outcomes, highlighting the need for biopsy strategies that detect mpMRI-invisible tumors.

Identifiers

PMID32914029
PMCPMC7446477
OpenAlexW2949747738

What OpenQuestion holds

Textmetadata
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.