Skip to main content
Clinical Trials/NL-OMON22061
NL-OMON22061
Recruiting
N/A

'PRIAS: Prostate cancer Research International: Active Surveillance - guideline and study for the expectant management of localized prostate cancer with curative intent'.

Erasmus MC, Rotterdam.0 sites2,000 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate cancer, overdiagnosis, overtreatment, active surveillance
Sponsor
Erasmus MC, Rotterdam.
Enrollment
2000
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Prospective validation of active surveillance in prostate cancer: the PRIAS study.
van den Bergh RCN, Roemeling S, Roobol MJ, Roobol W, Schröder FH, Bangma CH.
Eur Urol. 2007 Dec;52(6):1560-3. PMID: 17532115.

The Prostate cancer Research International: Active Surveillance study.
Bangma CH, Bul M, Roobol M.
Curr Opin Urol. 2012 May;22(3):216-21. doi:
10.1097/MOU.0b013e328351dcc7. Review.
PMID:22453333

Active surveillance for low-risk prostate cancer worldwide: the PRIAS study.
Bul M, Zhu X, Valdagni R, Pickles T, Kakehi Y, Rannikko A, Bjartell A, van der Schoot DK, Cornel EB, Conti GN, Boevé ER, Staerman F, Vis-Maters JJ, Vergunst H, Jaspars JJ, Strölin P, van Muilekom E, Schröder FH, Bangma CH, Roobol MJ.
Eur Urol. 2013 Apr;63(4):597-603. doi:
10.1016/j.eururo.2012.11.005. Epub 2012 Nov 12. PMID:23159452

A Decade of Active Surveillance in the PRIAS Study: An Update and Evaluation of the Criteria Used to Recommend a Switch to Active Treatment.
Bokhorst LP, Valdagni R, Rannikko A, Kakehi Y, Pickles T, Bangma CH, Roobol MJ; PRIAS study group..
Eur Urol. 2016 Dec;70(6):954-960. doi:
10.1016/j.eururo.2016.06.007. Epub 2016 Jun 19. PMID:27329565

Complications after prostate biopsies in men on active surveillance and its effects on receiving further biopsies in the Prostate cancer Research International: Active Surveillance (PRIAS) study.
Bokhorst LP, Lepistö I, Kakehi Y, Bangma CH, Pickles T, Valdagni R, Alberts AR, Semjonow A, Strölin P, Montesino MF, Berge V, Roobol MJ, Rannikko A.
BJU Int. 2016 Sep;118(3):366-71. doi: 10.1111/bju.13410. Epub 2016 Feb 12.
PMID:26765682

Compliance Rates with the Prostate Cancer Research International Active Surveillance (PRIAS) Protocol and Disease Reclassification in Noncompliers.
Bokhorst LP, Alberts AR, Rannikko A, Valdagni R, Pickles T, Kakehi Y, Bangma CH, Roobol MJ; PRIAS study group..
Eur Urol. 2015 Nov;68(5):814-21. doi: 10.1016/j.eururo.2015.06.012. Epub 2015 Jun 29.
PMID:26138043

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Erasmus MC, Rotterdam.

Eligibility Criteria

Inclusion Criteria

  • 1\) Histologically proven adenocarcinoma of the prostate.
  • 2\) Men should be fit for curative treatment.
  • 3\) PSA\-level at diagnosis ≤ 10 ng/mL.
  • 4\) PSA density (PSA D) less than 0\.2\.
  • 5\) Clinical stage T1C or T2\.
  • 6\) Gleason score 3\+3\=6\.
  • 7\) One or 2 biopsy cores invaded with prostate cancer:
  • If an MRI, including targeted biopsies on positive lesions, is done at inclusion, there is no limit in the number of positive cores (that is, more than two, and no limit in the % of cancer present in the cores).
  • If saturation biopsies (either transperineal or transrectal) are done 15% of the cores can be positive with a maximum of 4\. (i.e. \<20 cores 2 cores can be positive (standard), 20\-26 cores 3 cores can be positive, \>26 cores 4 cores can be positive) (all other inclusion criteria still apply).
  • 8\) Participants must be willing to attend the follow\-up visits.

Exclusion Criteria

  • 1\) Men who can not or do not want to be radiated or operated.
  • 2\) A former therapy for prostate cancer.

Outcomes

Primary Outcomes

Not specified

Similar Trials