Evidence map›Paper›PMID 26988552›Full record

ReviewWorld journal of urology2016

Non-metastatic castrate-resistant prostate cancer: a call for improved guidance on clinical management.

Francois Rozet, Thierry Roumeguère, Martin Spahn, Dirk Beyersdorff, Peter Hammerer

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in World journal of urology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02867020 (Phase II Randomized Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

NCT02867020 phase2completednot on this mapstarted 2017, after this paper: background citation

Phase II Randomized Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels

TypeinterventionalSponsorLatin American Cooperative Oncology GroupRan2017 to 2021Enrolled128ConditionsProstate CancerArmsApalutamide, Abiraterone, ADT, Prednisone
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Apalutamide and its use in the treatment of prostate cancer.Future oncology (London, England) · 2019
    Review
  9. Review
  10. Prostate Cancer in Latin America: Challenges and Recommendations.Cancer control : journal of the Moffitt Cancer Center
    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

5 authors.

Francois RozetDepartment of Urology, L'Institut Mutualiste Montsouris, 42 Boulevard Jourdan, 75014, Paris, France. francois.rozet@imm.fr.
Thierry RoumeguèreDepartment of Urology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
Martin SpahnDepartment of Urology, Bern University Hospital, Bern, Switzerland.
Dirk BeyersdorffClinic for Diagnostic and Interventional Radiology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Peter HammererDepartment of Urology, Academic Hospital Braunschweig, Braunschweig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuidelines on the clinical management of non-metastatic castrate-resistant prostate cancer (nmCRPC) generally focus on the need to continue androgen deprivation therapy and enrol patients into clinical trials of investigational agents. This guidance reflects the lack of clinical trial data with established agents in the nmCRPC patient population and the need for trials of new agents.

aimTo review the evidence base and consider ways of improving the management of nmCRPC.

conclusionUpon the development of castrate resistance, it is essential to rule out the presence of metastases or micrometastases by optimising the use of bone scans and possibly newer procedures and techniques. When nmCRPC is established, management decisions should be individualised according to risk, but risk stratification in this diverse population is poorly defined. Currently, prostate-specific antigen (PSA) levels and PSA doubling time remain the best method of assessing the risk of progression and response to treatment in nmCRPC. However, optimising imaging protocols can also help assess the changing metastatic burden in patients with CRPC. Clinical trials of novel agents in nmCRPC are limited and have problems with enrolment, and therefore, improved risk stratification and imaging may be crucial to the improved management. The statements presented in this paper, reflecting the views of the authors, provide a discussion of the most recent evidence in nmCRPC and provide some advice on how to ensure these patients receive the best management available. However, there is an urgent need for more data on the management of nmCRPC.

Indexed as

Diagnostic ImagingDisease ManagementProstatic Neoplasms, Castration-ResistantAndrogen AntagonistsAntineoplastic Agents, HormonalDisease ProgressionHumansMaleProstate-Specific AntigenAndrogen AntagonistsAntineoplastic Agents, HormonalProstate-Specific AntigenImagingIndividualised managementManagementNon-metastatic castrate-resistant prostate cancer

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.