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NCT Number: NCT06776172

Extended vs. No Pelvic Lymph Node Dissection During Radical Prostatectomy. DISSECTION 2.0.

The aim of the DISSECTION 2.0 study is to determine whether extended pelvic lymph node dissection (ePLND) provides a therapeutic benefit for high-risk prostate cancer patients by improving cancer staging and potentially removing micrometastatic disease, ultimately improving their outcomes.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Cantonal Hospital Aarau, Aarau, Switzerland

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About this study

Prostate cancer is the second most common cancer in men globally and a major cause of cancer deaths in Europe. For men with localized prostate cancer (PCa) and a life expectancy of over 10 years, radical prostatectomy (RP) is the standard treatment. It improves survival compared to conservative management. However, there is debate about de benefit of pelvic lymph node dissection (PLND), the removal of lymph nodes in the pelvis, during RP. While PLND can be omitted in low risk PCa patients, extended PLND (ePLND) is recommended in PCa patients at high-risk for recurrence in order to improve nodal staging The DISSECTION 2.0 study aims to investigate whether extended PLND (ePLND) provides additional benefits for men with high-risk PCa. The hypothesis is that ePLND might help by removing undetectable cancer cells (micrometastases) in the lymph nodes or by better staging the disease for treatment planning. While imaging techniques like PSMA-PET are good at detecting cancer spread, they still miss approximately 60% of cancer-bearing lymph nodes, leaving room for ePLND to potentially improve outcomes.

ePLND involves removing more lymph nodes than standard PLND, leading to better detection of cancer spread. However, it also increases surgery time and complications slightly, though serious complications are rare.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years and life expectancy >15 years
  • Any biopsy-proven WHO/ISUP grade groups III-V PCa
  • High-risk prostate cancer defined as:
  • Any biopsy-proven WHO/ISUP grade group III-V PCa or
  • ISUP grade group II and PSA > 20 ng/ml
  • PSMA-PET: negative staging for regional and distant metastasis
  • multidisciplinary tumorboard recommendation for radical prostatectomy
  • WHO performance status 0-1
  • Adequate condition (ASA ≤ III) for general anesthesia and RP

Exclusion criteria

  • ISUP grade group I PCa and cT1 or cT2 (MRI)
  • cT4 (MRI) PCa
  • PSMA-PET: positive staging for local and distant metastasis
  • Any prior neoadjuvant, local or systemic treatment for PCa
  • Previous PLND or pelvic radiotherapy
  • Patients with a prior malignancy and treated with curative intention are eligible if all treatment of that malignancy was completed at least 2 years before registration and the patient has no evidence of disease at registration. Less than 2 years is acceptable for malignancies with low risk of recurrence and/or no late recurrence.
  • Any other serious underlying medical, psychiatric, psychological, familial, or geographical
  • condition, which in the judgment of the investigator may interfere with the planned
  • staging, treatment and follow-up, which affect patient compliance or place the patient at
  • high risk from treatment-related complications.
  • Vulnerable men (participants incapable of judgment or participants under tutelage) will not be included in the study.

Treatment and study plan

Extended Pelvic Lymph Node Dissection

Procedure

Extended pelvic lymph node dissection during radical prostatectomy

Other names: Extended Lymph Node Dissection

Primary outcomes

  1. Prostate specific antigen (PSA) persistence

    Time frame: 3 month (+/- 2 weeks) postoperatively

    defined as failure to reach a PSA value of <0.1 ng/ml

  2. Biochemical recurrence free survival (BCRFS)

    Time frame: within 24 months post surgery

    time from randomization to biochemical recurrence, defined as serum PSA level ≥ 0.2 ng/ml

Secondary outcomes

  1. PSA persistence (PSAP) above detection limit

    Time frame: postoperative to the end of the study at 10-15 years

    cut-off ≥ 0.03 ng/ml

  2. Initiation time of adjuvant or salvage therapies

    Time frame: postoperative to the end of the study at 10-15 years

    Calculated from randomization to the start of any adjuvant or salvage therapy.

    Salvage radiotherapy (SRT) to the prostatic fossa only excluding lymphatics and without androgen deprivation therapy) will not count as an event for this endpoint if:

    • A PSMA-PET-computed tomography prior to SRT was negative for disease beyond the prostatic fossa, and
    • the SRT led to a PSA <0.1 ng/ml (PSAP) or ≤ 0.2 ng/ml (biochemical recurrence-free survival, BCRFS), respectively.
  3. Time to loco-regional recurrence

    Time frame: from randomization to end of study at 10-15 years

    Calculated from randomization until the first local (prostate bed) or regional (within the extent of the ePLND template) recurrence.

  4. Localization of progression

    Time frame: from randomization to end of study at 10-15 years

    Prostate-specific membrane antigen positron emission tomography (PSMA-PET)

  5. Time to distant metastasis

    Time frame: postoperative to the end of the study at 10-15 years

    Calculated from randomization until the first occurrence of distant metastasis.

  6. Prostate cancer-specific survival

    Time frame: postoperative to the end of the study at 10-15 years

    death due to prostate cancer

  7. Overall survival

    Time frame: postoperative to the end of the study at 10-15 years

    death from any cause

  8. Intraoperative complications

    Time frame: during surgery

    Documented using the CLASSintra classification

  9. Postoperative complications

    Time frame: postoperative up to 10-15 years

    Assessed using the Clavien-Dindo classification

  10. Adverse events (AEs) related to ePLND

    Time frame: postoperative up to 10-15 years

    Categorized according to CTCAE version 5.0

  11. Patient-reported outcome measures (PROMs)

    Time frame: postoperative up to 10-15 years

    tracked using the Expanded Prostate Cancer Index Composite (EPIC)-26 questionnaire Score 1-100 (100 indicates best quality of life score)

Other outcomes

  1. Evaluation of risk prediction for nodal invasion

    Time frame: postoperative to the end of the study at 10-15 years

    from prostate biopsy results

  2. Evaluation of the potential value of unilateral ePLND

    Time frame: postoperative to the end of the study at 10-15 years

Study contacts

Contact information is provided by the study sponsor or research team.

Cyrill Rentsch, Prof. Dr. med.

CONTACT

[email protected]

+41 61 26 87122

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Official study title

Extended Pelvic Lymph Node Dissection vs. No Pelvic Lymph Node Dissection at Radical Prostatectomy in PSMA PET Negative Staged Men: A Multicenter, Randomized Phase III Trial

Important dates

Study start
2025
Primary completion
2027
Study completion
2040
First posted
Jan 15, 2025
Registry last updated
Jul 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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