Evidence map›Paper›PMID 37101776›Full record

ArticleEuropean urology open science2023

Prognostic Value of the Intermediate-risk Feature in Men with Favorable Intermediate-risk Prostate Cancer: Implications for Active Surveillance.

Michael V Sherer, Austin J Leonard, Tyler J Nelson, P Travis Courtney, Kripa Guram, Gustavo Rodrigues De Moraes, Juan Javier-Desloges, Christopher Kane, Rana R McKay, Brent S Rose and 1 more

Abstract read
In one paragraph

Article in European urology open science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Michael V ShererDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Austin J LeonardDepartment of Urology, University of California San Diego, La Jolla, CA, USA.
Tyler J NelsonDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
P Travis CourtneyDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Kripa GuramDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Gustavo Rodrigues De MoraesDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Juan Javier-DeslogesDepartment of Urology, University of California San Diego, La Jolla, CA, USA.
Christopher KaneDepartment of Urology, University of California San Diego, La Jolla, CA, USA.
Rana R McKayDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Brent S RoseDepartment of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
Aditya BagrodiaDepartment of Urology, University of California San Diego, La Jolla, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Guidelines suggest that active surveillance (AS) may be considered for select patients with favorable intermediate-risk (fIR) prostate cancer. Objective: To compare the outcomes between fIR prostate cancer patients included by Gleason score (GS) or prostate-specific antigen (PSA). Most patients are classified with fIR disease due to either a 3 + 4 = 7 GS (fIR-GS) or a PSA level of 10-20 ng/ml (fIR-PSA). Previous research suggests that inclusion by GS 7 may be associated with worse outcomes. Design setting and participants: We conducted a retrospective cohort study of US veterans diagnosed with fIR prostate cancer from 2001 to 2015. Outcome measurements and statistical analysis: We compared the incidence of metastatic disease, prostate cancer-specific mortality (PCSM), all-cause mortality (ACM), and receipt of definitive treatment between fIR-PSA and fIR-GS patients managed with AS. Outcomes were compared with those of a previously published cohort of patients with unfavorable intermediate-risk disease using cumulative incidence function and Gray's test for statistical significance. Results and limitations: The cohort included 663 men; 404 had fIR-GS (61%) and 249 fIR-PSA (39%). There was no evidence of difference in the incidence of metastatic disease (8.6% vs 5.8%, Conclusions: There is no evidence of difference in oncological and survival outcomes between men with fIR-PSA and fIR-GS prostate cancer undergoing AS. Thus, presence of GS 7 disease alone should not exclude patients from consideration of AS. Shared decision-making should be utilized to optimize management for each patient. Patient summary: In this report, we compared the outcomes of men with favorable intermediate-risk prostate cancer in the Veterans Health Administration. We found no significant difference between survival and oncological outcomes.

Indexed as

Active surveillanceFavorable intermediate-risk prostate cancerShared decision-making

Identifiers

PMID37101776
PMCPMC10123417

What OpenQuestion holds

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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.