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A multicentre study in patients with localised prostate cancer for prediction of pathological stage of the radical prostatectomy and assessment of predictive factors of postoperative-recurrent.( Development of a Japanese Prostate Cancer Nomogram )

A multicentre study in patients with localised prostate cancer for prediction of pathological stage of the radical prostatectomy and assessment of predictive factors of postoperative-recurrent.( Development of a Japanese Prostate Cancer Nomogram ) - A multicentre study in patients with localised prostate cancer for prediction of pathological stage of the radical prostatectomy and assessment of prediction factors of postoperative-recurrent.( Development of a Japanese Prostate Cancer Nomogram )

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-C000000333
Enrollment
4000
Registered
2006-03-01
Start date
2002-05-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Interventions

None listed

Sponsors

Clinicopathological Research Group for Localized Prostate Cancer (CRPC)
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: [ Prospective study ] 1.Patients with localised prostate cancer who received radical prostatectomy (including laparoscopic surgery ) on and after 1st May 2002 (regardless of enforcement of neo-adjuvant therapy and adjuvant therapy). 2.Patients with PSA measurement by the equimolar PSA kit ( except for Merkit-M ) before enforcement of radical prostatectomy. 3.Patients with at least six or more systematic biopsies enforced under the ultrasonic guide. 4.Patients with evaluable clinical stage by TNM classification of malignant tumors ( UICC 1992.Ver.4 ). 5.Patients whose follow-up observation is possible, while measuring PSA periodically after enforcement of radical prostatectomy. (However, follow-up will not be done for patients who undergone adjuvant therapy.) The following patients who filled all of these five conditions. A: Neo-Adjuvant hormone therapy non-enforcing patients. B: Neo-Adjuvant hormone therapy enforcement patients. (Regardless of contents and period ) [ Retrospective study ] 1.Patients with localised prostate cancer patients who underwent radical prostatectomy (including laparoscopic surgery ) from 1st January 1997 to 30th April 2002 (Regardless of neo-adjuvant therapy and adjuvant therapy). 2.And other items are the same as the prospective study, except for the same standards for a positive study will be applied.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
1.Comparison of preoperative clinical data and histopathological findings of the biopsy specimen with histopathological findings of the radical prostatectomy specimen. 2.Prediction of PSA recurrence by the preoperative clinical data and histopathological findings of the biopsy specimen. 3.Prediction of PSA recurrence by histopathological findings of the radical prostatectomy specimen.

Countries

Japan

Contacts

Public ContactRyoko Fukunaga

Graduate School of Medical Sciences, Kyusyu University Department of Urology

hinyoki@uro.med.kyushu-u.ac.jp092-642-5603

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026