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The Prognostic Role of Lymph Node Dissection In Men With Prostate Cancer Treated With Radical Prostatectomy

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Pelvic lymph node dissection
Sponsored by
The Netherlands Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate Cancer, Lymph node dissection, Prostatectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male, aged ≥ 18 years
  • Prostate cancer patients with a Briganti calculated risk of LN metastases of 5-20% without evidence of metastases on Prostate-Specific Membrane Antigen (PSMA) PET/CT requiring an ePLND in the standard treatment
  • Scheduled for a (robot-assisted) laparoscopic radical prostatectomy
  • Written informed consent

Exclusion Criteria:

  • American Society of Anaesthesiology (ASA) classification > 3
  • Patients with a contradiction for a lymphadenectomy
  • Neoadjuvant hormone deprivation therapy
  • Absence or withdrawal of an informed consent
  • Evidence of metastases on pre-operative PSMA PET/CT

Sites / Locations

  • NKI-AVLRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Radical prostatectomy with an extended pelvic lymph node dissection

Radical prostatectomy without an extended pelvic lymph node dissection

Arm Description

According to the standard of care, patients in this arm will receive a radical prostatectomy with a standard bilateral ePLND. This includes the removal of lymph nodes within the obturator fossa and bilateral to the external iliac artery, internal iliac artery and common iliac artery up to the ureteral-vessel crossing.

Patients in this arm will undergo a radical prostatectomy without a bilateral extended pelvic lymph node dissection. In case of intraoperatively found suspicious lymph nodes, a lymphadenectomy is performed. According to the intention to treat principle, patients with intraoperatively removed lymph nodes remain included in the study.

Outcomes

Primary Outcome Measures

Persistent PSA rate
Persistent PSA is defined as a PSA value ≥ 0.1 ng/ml after radical prostatectomy

Secondary Outcome Measures

Biochemical recurrence (BCR) rate
BCR is defined as a PSA value ≥ 0.2 ng/ml after radical prostatectomy
Metastasis-free survival
This is defined as the time between radical prostatectomy to development of metastasis
Incidence of complications after surgery
According to Clavien-Dindo classification
Incidence of salvage therapy after primary surgery
I.e., androgen deprivation therapy, radiation therapy or salvage lymph node dissection
Global Quality of life after surgery
Quality of life (QoL) will be assessed with the EORTC Core Quality of Life questionnaire's (QLQ-C30) global QoL scale ranging from 0 to 100, higher scores indicate better QoL
Health-related quality of life of patients with prostate cancer
Health-related quality of life in prostate cancer patients will be assessed with the EORTC Quality of Life Questionnaire - Prostate Cancer Module (QLQ-PR25) with a scale ranging from 0 to 100, higher scores indicate either more symptoms (urinary, bowel, hormonal treatment-related symptoms) or higher levels of (sexual) activity or functioning
Urinary continence after surgery
Urinary continence will be assessed with the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) questionnaire, ranging from 0 (best) to 21 (worst)
Urinary voiding symptoms
Urinary voiding symptoms will be assessed with the International Prostatic Symptoms Score (IPSS), ranging from 0 (best) to 35 (worst)
Potency after surgery
Potency will be assessed with the International Index of Erectile Function (IIEF) questionnaire. The IIEF classifies the severity of erectile dysfunction into five categories stratified by score: No erectile dysfunction. Score: 26-30 Mild erectile dysfunction. Score: 22-25 Mild to moderate erectile dysfunction. Score: 17-21 Moderate erectile dysfunction. Score: 11-16 Severe erectile dysfunction. Score: 6-10.

Full Information

First Posted
August 26, 2021
Last Updated
November 17, 2021
Sponsor
The Netherlands Cancer Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05109910
Brief Title
The Prognostic Role of Lymph Node Dissection In Men With Prostate Cancer Treated With Radical Prostatectomy
Official Title
Prospective Randomized Controlled Trial To Evaluate The Prognostic Role of Lymph Node Dissection In Men With Prostate Cancer Treated With Radical Prostatectomy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 17, 2021 (Anticipated)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
November 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Netherlands Cancer Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
An extended pelvic lymph node dissection (ePLND) is the most accurate staging method to assess the presence of lymph node metastases in prostate cancer (PCa) patients. The therapeutic value, however remains unclear. Prospective randomized trials to address this void are lacking. Since in intermediate and a proportion of high risk PCa the risk of nodal metastases is generally below 25%, the vast majority of men undergo a procedure that has no oncological benefit, but is not without toxicity. Therefore, the investigators aim to compare the oncologic outcomes of intermediate- and high-risk PCa patients with an estimated risk of lymph node invasion of 5-20% undergoing a radical prostatectomy (RP) with or without an ePLND.
Detailed Description
The role of an extended pelvic lymph node dissection (ePLND) in patients undergoing radical prostatectomy (RP) remains controversial. An ePLND is the most accurate staging method to assess the presence of lymph node metastases. Lymph node involvement is associated with a significantly worse prognosis and may require immediate or delayed adjuvant therapy. However, an ePLND is associated with an increased risk of complications such as lymphoceles, thromboses and lymphedema, and prolongs surgery and patient recovery. Thus, the diagnostic advantage of PLND should be weighed against the potential morbidity. The therapeutic value of an ePLND remains especially unclear in PCa patients with an estimated risk of lymph node invasion (LNI) ≤ 20%, where only a minority of patients will have nodes harbouring metastases. Prospective trials to address this issue are still lacking.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, Lymph node dissection, Prostatectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
284 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Radical prostatectomy with an extended pelvic lymph node dissection
Arm Type
Active Comparator
Arm Description
According to the standard of care, patients in this arm will receive a radical prostatectomy with a standard bilateral ePLND. This includes the removal of lymph nodes within the obturator fossa and bilateral to the external iliac artery, internal iliac artery and common iliac artery up to the ureteral-vessel crossing.
Arm Title
Radical prostatectomy without an extended pelvic lymph node dissection
Arm Type
No Intervention
Arm Description
Patients in this arm will undergo a radical prostatectomy without a bilateral extended pelvic lymph node dissection. In case of intraoperatively found suspicious lymph nodes, a lymphadenectomy is performed. According to the intention to treat principle, patients with intraoperatively removed lymph nodes remain included in the study.
Intervention Type
Procedure
Intervention Name(s)
Pelvic lymph node dissection
Intervention Description
Bilateral extended pelvic lymph node dissection
Primary Outcome Measure Information:
Title
Persistent PSA rate
Description
Persistent PSA is defined as a PSA value ≥ 0.1 ng/ml after radical prostatectomy
Time Frame
6 months after surgery
Secondary Outcome Measure Information:
Title
Biochemical recurrence (BCR) rate
Description
BCR is defined as a PSA value ≥ 0.2 ng/ml after radical prostatectomy
Time Frame
3 years after surgery
Title
Metastasis-free survival
Description
This is defined as the time between radical prostatectomy to development of metastasis
Time Frame
3 years after surgery
Title
Incidence of complications after surgery
Description
According to Clavien-Dindo classification
Time Frame
3 and 6 months after surgery
Title
Incidence of salvage therapy after primary surgery
Description
I.e., androgen deprivation therapy, radiation therapy or salvage lymph node dissection
Time Frame
3 years after surgery
Title
Global Quality of life after surgery
Description
Quality of life (QoL) will be assessed with the EORTC Core Quality of Life questionnaire's (QLQ-C30) global QoL scale ranging from 0 to 100, higher scores indicate better QoL
Time Frame
6, 12, 24 and 36 months after surgery
Title
Health-related quality of life of patients with prostate cancer
Description
Health-related quality of life in prostate cancer patients will be assessed with the EORTC Quality of Life Questionnaire - Prostate Cancer Module (QLQ-PR25) with a scale ranging from 0 to 100, higher scores indicate either more symptoms (urinary, bowel, hormonal treatment-related symptoms) or higher levels of (sexual) activity or functioning
Time Frame
6, 12, 24 and 36 months after surgery
Title
Urinary continence after surgery
Description
Urinary continence will be assessed with the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) questionnaire, ranging from 0 (best) to 21 (worst)
Time Frame
6, 12, 24 and 36 months after surgery
Title
Urinary voiding symptoms
Description
Urinary voiding symptoms will be assessed with the International Prostatic Symptoms Score (IPSS), ranging from 0 (best) to 35 (worst)
Time Frame
6, 12, 24 and 36 months after surgery
Title
Potency after surgery
Description
Potency will be assessed with the International Index of Erectile Function (IIEF) questionnaire. The IIEF classifies the severity of erectile dysfunction into five categories stratified by score: No erectile dysfunction. Score: 26-30 Mild erectile dysfunction. Score: 22-25 Mild to moderate erectile dysfunction. Score: 17-21 Moderate erectile dysfunction. Score: 11-16 Severe erectile dysfunction. Score: 6-10.
Time Frame
6, 12, 24 and 36 months after surgery

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Presence of prostate cancer
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male, aged ≥ 18 years Prostate cancer patients with a Briganti calculated risk of LN metastases of 5-20% without evidence of metastases on Prostate-Specific Membrane Antigen (PSMA) PET/CT requiring an ePLND in the standard treatment Scheduled for a (robot-assisted) laparoscopic radical prostatectomy Written informed consent Exclusion Criteria: American Society of Anaesthesiology (ASA) classification > 3 Patients with a contradiction for a lymphadenectomy Neoadjuvant hormone deprivation therapy Absence or withdrawal of an informed consent Evidence of metastases on pre-operative PSMA PET/CT
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Henk G van der Poel, Prof
Phone
0205129111
Email
h.vd.poel@nki.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Hilda A de Barros, MD
Phone
0205129111
Email
h.d.barros@nki.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henk G van der Poel, Prof
Organizational Affiliation
The Netherlands Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
NKI-AVL
City
Amsterdam
ZIP/Postal Code
1066 CX
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
H.G van der Poel, Prof

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Prognostic Role of Lymph Node Dissection In Men With Prostate Cancer Treated With Radical Prostatectomy

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