Evidence map›Paper›PMID 40567132›Full record

ArticleCancer medicine2025

Understanding the Impact of Salvage Radiation on the Long-Term Natural History of Biochemically Recurrent Prostate Cancer After Radical Prostatectomy.

Spyridon P Basourakos, Stephen A Boorjian, Phillip J Schulte, Grant Henning, Jamie T O'Byrne, Matthew K Tollefson, Igor Frank, Abhinav Khanna, Ryan M Phillips, Bradley J Stish and 2 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. 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

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

4 citing papers in PubMed.

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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

12 authors.

Spyridon P BasourakosDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-7458-4593
Stephen A BoorjianDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Phillip J SchulteDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Grant HenningDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Jamie T O'ByrneDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Matthew K TollefsonDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Igor FrankDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Abhinav KhannaDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Ryan M PhillipsDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota, USA.
Bradley J StishDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota, USA.
R Jeffrey KarnesDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.
Vidit SharmaDepartment of Urology, Mayo Clinic, Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe natural history of biochemical recurrence (BCR) after radical prostatectomy (RP) remains understudied, with limited long-term data from large cohorts inclusive of both salvage radiotherapy (SRT)-treated and untreated patients. Herein, we sought to evaluate the outcomes of patients with BCR and the impact of SRT on disease progression. MATERIALS AND

methodsPatients undergoing RP who developed BCR (PSA ≥ 0.20 ng/mL) were included. Patients with BCR treated with SRT were compared to untreated patients using risk-set matching with time-dependent propensity scores. The primary outcome was metastases, analyzed using Kaplan-Meier and Cox models. The number needed to treat (NNT) with SRT to prevent progression was derived at 5 and 15 years.

resultsAmong 6881 patients with BCR, 2109 received SRT. At a median follow-up of 10.2 years, 1147 patients developed metastases. The median PSA at the time of SRT was 0.50 ng/mL. After 1:1 propensity score matching (2109 patients per cohort), SRT significantly reduced the risk of metastases at 5 (12.7% vs. 19.3%, p < 0.0001) and 15 years (28.6% vs. 31.5%, p < 0.001). On multivariable analysis, SRT independently reduced metastasis risk (HR 0.75, 95% CI 0.63-0.90, p = 0.002), translating to NNT of 23 and 15 at 5 and 15 years, respectively. Interaction analyses between SRT and nodal status (p = 0.04) showed greater metastasis risk reduction in pN+ (HR 0.41, 95% CI 0.22-0.77, p = 0.005) compared to pN- disease (HR 0.81, 95% CI 0.67-0.97, p = 0.02).

conclusionsMost patients with BCR post-RP do not progress to metastasis. For those who do progress, SRT inarguably improves the oncologic outcomes in the BCR setting. However, careful patient selection and shared decision making should be encouraged in order to limit overtreatment and side effects.

Indexed as

Neoplasm Recurrence, LocalProstatectomyProstatic NeoplasmsSalvage TherapyAgedDisease ProgressionFollow-Up StudiesHumansKaplan-Meier EstimateMaleMiddle AgedProstate-Specific AntigenRetrospective StudiesTreatment OutcomeProstate-Specific Antigenbiochemical recurrenceprostate cancersalvage radiation therapy

Identifiers

PMID40567132
PMCPMC12198693

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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.