Evidence map›Paper›PMID 38371200›Full record

ArticleBJUI compass2024

Low PSA radiographic disease progression on C11-choline PET.

Ahmed M Mahmoud, Mohamed E Ahmed, A Tuba Kendi, Matthew Thorpe, Geoffrey B Johnson, Irbaz Bin Riaz, Jacob J Orme, Eugene D Kwon, Jack R Andrews, Daniel S Childs

Open access · goldAbstract read
In one paragraph

Article in BJUI compass, 2024. 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
0.5field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

10 authors at 3 institutions in 1 country.

Ahmed M MahmoudDepartment of Urology Mayo Clinic Rochester Minnesota USA.ORCID https://orcid.org/0000-0003-2002-685X
Mohamed E AhmedDepartment of Urology Mayo Clinic Rochester Minnesota USA.
A Tuba KendiDepartment of Radiology, Division of Nuclear Medicine Mayo Clinic Rochester Minnesota USA.
Matthew ThorpeDepartment of Radiology, Division of Nuclear Medicine Mayo Clinic Rochester Minnesota USA.
Geoffrey B JohnsonDepartment of Radiology, Division of Nuclear Medicine Mayo Clinic Rochester Minnesota USA.
Irbaz Bin RiazDepartment of Medical Oncology Mayo Clinic Scottsdale Arizona USA.
Jacob J OrmeDepartment of Medical Oncology Mayo Clinic Rochester Minnesota USA.
Eugene D KwonDepartment of Urology Mayo Clinic Rochester Minnesota USA.
Jack R AndrewsDepartment of Urology Mayo Clinic Arizona Phoenix Arizona USA.
Daniel S ChildsDepartment of Medical Oncology Mayo Clinic Rochester Minnesota USA.
Mayo Clinic · USMayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: For men with prostate cancer, radiographic progression may occur without a concordant rise in prostate-specific antigen (PSA). Our study aimed to assess the prevalence of radiographic progression using C-11 choline positron emission tomography (PET) imaging in patients achieving ultra-low PSA values and to evaluate clinical outcomes in this patient population. Methods: In a single institution study, we reviewed the prospectively maintained Mayo Clinic C-11 Choline PET metastatic prostate cancer registry to identify patients experiencing radiographic disease progression (rDP) on C-11 choline PET scan while the PSA value was less than 0.5 ng/mL. Disease progression was confirmed by tissue biopsy or response to subsequent therapy. Clinicopathologic variables were abstracted by trained research personnel. Overall survival was estimated using the Kaplan-Meier method. Intergroup differences were assessed using the log-rank test. A univariate and multivariate Cox regression model was performed to investigate variables associated with poor survival after rDP. Results: A total of 1323 patients within the registry experienced rDP between 2011 and 2021, including 220 (16.6%) men with rDP occurring at low PSA level. A median (interquartile range [IQR]) of 54.7 (19.7-106.9) months elapsed between the time of prostate cancer diagnosis and low PSA rDP, during which 173 patients (78%) developed castration-resistant prostate cancer (CRPC). Sites of low PSA rDP included local recurrence ( Conclusions: Men with prostate cancer commonly experience metastatic progression at very low or even undetectable PSA levels. Periodic imaging, even at low absolute PSA values, may result in more timely identification of disease progression.

Indexed as

C11‐choline PETlow PSAprostate cancer

Identifiers

PMID38371200
PMCPMC10869648
OpenAlexW4387939801

What OpenQuestion holds

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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.