DEfeating PEnile CAncer-2

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity Hospital Tuebingen

About this trial

Open inguinal lymphadenectomy (O-ILAD) is the current standard of care for invasive staging and simultaneously the curative approach for patients with PeCa and elevated risk for or clinically detectable lymphatic disease in the groin. The high rate of complications of this surgical procedure, which are often mutilating and associated with a long-term convalescence, leads to a critical delay in initiation of adjuvant systemic therapy. Being in apprehension of these postsurgical adversities, physicians are often reluctant with indicating this procedure, thus depriving their patients of the vital prognosis-relevant care. In the sum, these obstacles inevitably result in inferior oncologic outcomes. Aiming to decrease postsurgical detrimental sequelae, several attempts to modify radicality of the technique, including inter alia a radioguided approach of sentinel lymph node resection, have been presented in the last decades. Unfortunately, utilization of the sentinel lymph node technique outside of a few highly specialized referral centers is prone to a significant false negativity, while other approaches are associated with inconsistent oncological and perioperative outcomes, hence precluding a general breakthrough in the surgical management of the groin lymph nodes. Thus, a high unmet medical need exists for the establishment of an approach with the lowest possible rate of complications and at the same time the optimal oncological safety.

In this context, preliminary evidence from small sample studies points to a promising potential of minimally invasive surgery to be further tested in the setting of inguinal lymphadenectomy. A recent retrospective single-center report on robot-assisted inguinal lymphadenectomy (R-ILAD) showed that the rate of major complications was only as low as 2%. On the contrary, the rate of major complications in our own and other O-ILAD series was approx. 30%.

DEPECA-2 is a prospective randomized multicenter trial, in which R-ILAD will be tested vs. O-ILAD on the 1b level of evidence for the first time. The scientific value of the project is significantly substantiated by a comprehensive translational research program, which includes inflammatory and oncologic biomarker research, as well as functional validation in preclinical models. The results of this trial will foster further optimization of outcomes in the surgical management of PeCa.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1. Patient has provided written informed consent.

2. Male patient ≥ 18 years at time of signing the informed consent form.

3. Patient has histologically proven penile squamous cell carcinoma.

pT1a, G2, cN0 OR

Disqualifiers

1. Patients has inguinal bulky disease ≥ 4 cm (determined by ultrasound or cross-sectional imaging).

2. Patient has distant metastases.

3. Patient receives or is scheduled for neoadjuvant chemotherapy for PeCa.

4. Patient received previous major inguinal surgery (transabdominal laparoscopic inguinal hernia repair is permitted), sentinel or other lymph node resection or radiotherapy in the groin or pelvic area.

Trial design

Design model

Parallel

Treatments tested in this trial

  • open inguinal lymphadenectomy

    Procedure/Surgery

    open inguinal lymphadenectomy

  • robot-assisted inguinal lymphadenectomy

    Procedure/Surgery

    robot-assisted inguinal lymphadenectomy

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: open inguinal lymphadenectomyActive comparator 1 intervention
Group B: robot-assisted inguinal lymphadenectomyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Rate of postoperative complications ≥ grade 3 within 3 months after surgery

Rate of postoperative complications ≥ grade 3 within 3 months after surgery according to Clavien-Dindo classification (Dindo-2004)

Time frame
Up to 3 months

Secondary outcomes

1

Total complication rate

Total complication rate, defined as rate of all post-operative complications that occurred within 4 weeks, 3 and 6 months post-surgery

Time frame
Up to 6 months
2

Drain-free rate

Drain-free rate on day 21, day 28 and day 35 after surgery (drain removal if output \< 30 mL/d on at least 3 consecutive days), defined as proportion of patients who no longer have a drain on day 21, 28 and 35 after surgery

Time frame
Up to 35 days
3

Length of drain in situ

Length of drain in situ, defined as time from surgery to the day of drain removal

Time frame
Up to drain removal, an average of 3 weeks
4

Percentage of patients with surgical site infections requiring antibiotic treatment

Percentage of patients with surgical site infections requiring antibiotic treatment

Time frame
Up to 6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital Tuebingen

Lead sponsor

Frankfurt Institute of Clinical Cancer Research (IKF)

Collaborator