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Clinical Trials/NCT01812902
NCT01812902
Completed
N/A

Prospective Randomized Study Comparing Extended With Limited Pelvic Lymphadenectomy in Intermediate and High Risk Prostate Cancer Patients Undergoing Radical Prostatectomy

University of Sao Paulo1 site in 1 country260 target enrollmentFebruary 2012
ConditionsProstate Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
University of Sao Paulo
Enrollment
260
Locations
1
Primary Endpoint
Biochemical relapse-free survival
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Prostate cancer is currently the second most common cause of cancer death in men in Western countries. Lymphadenectomy is the gold standard procedure for staging pelvic lymph node and is classically indicated in intermediate and high risk prostate cancer patients and is held at the same time of prostatectomy. A traditionally pelvic lymphadenectomy covers the obturator chain bilaterally. Recently, some studies have demonstrated the existence of lymph node involvement outside the traditional boundaries of classical lymphadenectomy, recommending therefore extended dissection; this also includes the external / internal / common iliac chains and presacral. Thus lymphadenectomy, according to these authors, would also has a therapeutic role, besides helping in better staging. Although some retrospective studies report an association between lymphadenectomy and tumor progression, the exact impact of extended lymphadenectomy in oncological outcome of patients with prostate cancer is not clearly established, mainly by lack of prospective randomized studies on the subject . The study objectives are to compare the oncologic results of extended lymphadenectomy versus limited in order to elucidate the role of extended dissection in lymph node staging and results of treatment in terms of increased tumor cure. The investigators also intend to identify patients who may benefit from oncologically extended procedure. To do this, the investigators will evaluate prospectively patients diagnosed with prostate cancer at intermediate or high risk indicating lymphadenectomy and radical prostatectomy. These patients will be randomized to the extended versus limited lymphadenectomy and the investigators will compare the lymph node metastasis and pattern of spread of prostate cancer, as well as biochemical relapse-free survival, freedom from progression to metastasis and cancer-specific survival.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
April 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marcos Francisco Dall'Oglio

M.D. Phd

University of Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Prostate Cancer patients with intermediate or high risk and with indication of radical prostatectomy and LND
  • Absence of bone metastasis or other organ imaging test (MRI or scintigraphy)
  • Absence of hormone treatment
  • Absence of radiotherapy
  • Signing an informed consent
  • Availability and adequacy of lymph node tissue samples to perform the immunohistochemical

Exclusion Criteria

  • Life expectancy less than 10 years
  • Absence of clinical conditions for the procedure
  • Laparoscopic or perineal surgery
  • Presence of bone or visceral metastasis
  • Neoadjuvant treatment
  • Another malignant neoplasia
  • Prior abdominal or pelvic surgery

Outcomes

Primary Outcomes

Biochemical relapse-free survival

Time Frame: Five years

Secondary Outcomes

  • Cancer specific survival(10 years)
  • Staging(One Month)

Study Sites (1)

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