Evidence map›Paper›PMID 25408810›Full record

ArticleCanadian Urological Association journal = Journal de l'Association des urologues du Canada2014

Active surveillance in patients with a PSA >10 ng/mL.

Paul Toren, Lih-Ming Wong, Narhari Timilshina, Shabbir Alibhai, John Trachtenberg, Neil Fleshner, Antonio Finelli

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Article in Canadian Urological Association journal = Journal de l'Association des urologues du Canada, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Paul TorenDepartment of Urologic Sciences, University of British Columbia, Vancouver, BC;
Lih-Ming WongDepartment of Urology, St. Vincent's Hospital and Austin Health, University of Melbourne, Victoria, Australia;
Narhari TimilshinaDepartment of Surgery (Urology), University of Toronto, Princess Margaret Hospital, Toronto, ON;
Shabbir AlibhaiDepartment of Medicine and Institute of Health Policy, Management, and Evaluation, University Health Network and University of Toronto, Toronto, ON.
John TrachtenbergDepartment of Surgery (Urology), University of Toronto, Princess Margaret Hospital, Toronto, ON;
Neil FleshnerDepartment of Surgery (Urology), University of Toronto, Princess Margaret Hospital, Toronto, ON;
Antonio FinelliDepartment of Surgery (Urology), University of Toronto, Princess Margaret Hospital, Toronto, ON;

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe use of prostate-specific antigen (PSA) in active surveillance (AS) for prostate cancer is controversial. Some consider it an unreliable marker and others as sufficient evidence to exclude patients from AS. We analyzed our cohort of AS patients with a PSA over 10 ng/mL.

methodsWe included patients who had clinical T1c-T2a Gleason ≤6 disease, and ≤3 positive cores with ≤50% core involvement at diagnostic biopsy and ≥2 total biopsies. Patients were divided into 3 groups: (1) those with baseline PSA >10 ng/mL, (2) those with a PSA rise >10 ng/mL during follow-up; and (3) those with a PSA <10 ng/mL throughout AS. Adverse histology was defined as biopsy parameters exceeding the entry criteria limits. We further compared this cohort to a concurrent institutional cohort with equal biopsy parameters treated with immediate radical prostatectomy.

resultsOur cohort included 698 patients with a median follow-up of 46.2 months. In total, 82 patients had a baseline PSA >10 ng/mL and 157 had a PSA rise >10 ng/mL during surveillance. No difference in adverse histology incidence was detected between groups (p = 0.3). Patients with a PSA greater than 10 were older and had higher prostate volumes. Hazard ratios for groups with a PSA >10 were protective against adverse histology. Larger prostate volume and minimal core involvement appear as factors related to this successful selection of patients to be treated with AS.

conclusionThese results suggest that a strict cut-off PSA value for all AS patients is unwarranted and may result in overtreatment. Though lacking long-term data and validation, AS appears safe in select patients with a PSA >10 ng/mL and low volume Gleason 6 disease.

Identifiers

PMID25408810
PMCPMC4216302

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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.