Evidence map›Paper›PMID 36765111›Full record

ArticleProstate cancer and prostatic diseases2023

The natural history of a delayed detectable PSA after radical prostatectomy.

Julie A Szymaniak, Samuel L Washington, Janet E Cowan, Matthew R Cooperberg, Peter E Lonergan, Hao G Nguyen, Maxwell V Meng, Peter R Carroll

Open access · hybridAbstract read
In one paragraph

Article in Prostate cancer and prostatic diseases, 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
1.8field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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

8 authors at 2 institutions in 2 countries.

Julie A SzymaniakDepartment of Urology, University of California, San Francisco, CA, USA. Julie.Szymaniak@UCSF.edu.ORCID 0000-0002-0640-4335
Samuel L WashingtonDepartment of Urology, University of California, San Francisco, CA, USA.ORCID 0000-0002-2467-6115
Janet E CowanDepartment of Urology, University of California, San Francisco, CA, USA.
Matthew R CooperbergDepartment of Urology, University of California, San Francisco, CA, USA.
Peter E LonerganDepartment of Urology, St. James's Hospital, Dublin, Ireland.ORCID 0000-0001-7233-8156
Hao G NguyenDepartment of Urology, University of California, San Francisco, CA, USA.
Maxwell V MengDepartment of Urology, University of California, San Francisco, CA, USA.
Peter R CarrollDepartment of Urology, University of California, San Francisco, CA, USA.
University of California, San Francisco · USTrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMen with a detectable PSA after radical prostatectomy (RP) are often offered salvage therapy while those with an undetectable PSA are monitored. We aim to better characterize the natural history of men with an initially undetectable PSA who subsequently developed a detectable PSA > 6 months after RP.

methodsRetrospective analysis of men who underwent RP for clinically localized prostate cancer at the University of California, San Francisco from 2000 to 2022. The primary outcome was biochemical recurrence, defined as 2 consecutive PSA > = 0.03 ng/mL starting 6 months after surgery. Secondary outcomes were salvage treatment, post-salvage treatment, metastasis free survival (MFS), prostate cancer specific mortality (PCSM), and all-cause mortality (ACM). This cohort was compared to a previously described cohort who had an immediately detectable post-operative PSA.

resultsFrom our cohort of 3348 patients, we identified 2868 men who had an undetectable post-op PSA. Subsequently, 642 men had a delayed detectable PSA at a median of 25 months (IQR 15, 43) with median follow-up of 72 months after RP. PSA at time of failure was <0.10 ng/mL for 65.7% of men. Of those with a delayed detectable PSA, 46% underwent salvage treatment within 10 years after RP at a median PSA of 0.08 ng/mL (IQR 0.05, 0.14). High CAPRA-S score (HR 1.09, CI 1.02-1.17, p = 0.02) and PSA doubling time (PSA-DT) of <6 months (HR 7.58, CI 5.42-10.6, p < 0.01) were associated with receiving salvage treatment. After salvage treatment, 62% of men had recurrent PSA failure within 10 years. Overall, MFS was 92%, PCSM 3%, and ACM 6% at 10 years. For those who received tertiary treatment for recurrent PSA failure, MFS was 54%, PCSM 23% and ACM 23% at 10 years' time.

conclusionsMen who develop a detectable PSA > 6 months post-operatively may have excellent long-term outcomes, even in the absence of salvage therapy.

Indexed as

Prostatic NeoplasmsHumansMaleNeoplasm Recurrence, LocalProstateProstatectomyProstate-Specific AntigenRetrospective StudiesSalvage TherapyProstate-Specific Antigen

Identifiers

PMID36765111
PMCPMC10638081
OpenAlexW4319925020

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Registered trials

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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.