PRIMETEST II - Clinical Stage II A/B Seminoma Treated With RA-RPLND

NCT ID: NCT06144736

Last Updated: 2025-09-15

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-08-28
• Study Completion Date: 2029-08-31

Brief Summary

PRIMETEST II is an interventional study involving low-volume metastatic seminoma. It explores a novel approach using robot-assisted primary retroperitoneal lymph node dissection, aiming to reduce long-term side effects and improve quality of life. By identifying factors predicting cancer recurrence, the study hopes to tailor treatments for better outcomes. The approach could potentially spare patients from chemotherapy induced long-term side effects while maintaining excellent survival rates, presenting a promising shift in testicular cancer care for this specific patient group.

Detailed Description

Testicular cancer stands as the most prevalent cancer among young men, boasting a highly favorable prognosis characterized by almost unaltered long-term survival even in advanced stages. However, traditional treatments like chemotherapy and radiation are linked to significant long-term toxicity and increased rates of secondary malignancies. Particularly, late toxicities, mainly cardiovascular, substantially diminish overall survival by approximately 6-7 years. To circumvent unnecessary acute and long-term toxicities associated with radiation or chemotherapy, it's crucial to explore alternative therapeutic avenues through personalized, less toxic approaches.

Building upon the hypothesis-generating PRIMETEST I study, PRIMETEST II is a single-arm, non-randomized prospective study. It aims to explore novel and personalized predictive parameters for recurrence following a robot-assisted primary retroperitoneal lymph node dissection (pRA-RPLND) in patients with clinical stage IIA/B seminoma (involving low-volume metastatic disease up to 5 cm). These patients represent a rare subgroup among testicular cancer patients, making a randomized comparison of treatment options impractical due to their low prevalence. The overarching goal is to reduce long-term toxicity in this young cohort of cancer patients and enhance their quality of life through personalized clinical and molecular predictions.

PRIMETEST I has indicated that pRA-RPLND in patients with clinical stage IIA/B seminoma led to a 70% recurrence-free survival at 32 months' follow-up. These findings suggest that pRA-RPLND could serve as an alternative to standard therapies (chemotherapy, radiotherapy) for a highly selective group of patients, effectively preventing excessive toxicity. PRIMETEST I has already identified several potential factors that predict which patients are more likely to benefit from surgical therapy alone.

In the novel prospective setting of PRIMETEST II, the study tests the identified predictive factors for recurrence. Patients exhibiting presumably low-risk features (about 70% of patients) will continue with surgery alone. Those with a presumed higher risk of recurrence will undergo robot-assisted surgery and have the option of receiving adjuvant treatment (one cycle of cisplatin, etoposide, and bleomycin). The primary endpoint is a three-year recurrence-free survival, estimated to exceed 90%. Additional objectives include exploring new predictors of recurrence at both molecular and clinical levels by analyzing serum and tissue samples from the primary tumor and metastases.

This innovative approach anticipates that 70% of patients will avoid long-term toxicity and experience excellent recurrence-free survival rates comparable to standard chemotherapy or radiation therapy.

Conditions

Seminoma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Low risk

Criteria for "low risk":

• Absence of "high risk" criteria
• Previous carboplatin therapy post orchiectomy
• Exclusion of malignancy in the RPLND histology

Group Type: EXPERIMENTAL

Robot-assisted retroperitoneal lymph node dissection

Intervention Type: PROCEDURE

Robot-assisted, if possibe ipsilateral nerve-sparing, retroperitoneal lymph node dissection and metastasis resection in a unilateral dissection field ("template")

High risk

Criteria for "high risk":

• Clinical stage II at initial diagnosis
• Primary tumor > 4 cm
• Infiltration of the "rete testis" in the primary tumor

Group Type: EXPERIMENTAL

Robot-assisted retroperitoneal lymph node dissection

Intervention Type: PROCEDURE

Robot-assisted, if possibe ipsilateral nerve-sparing, retroperitoneal lymph node dissection and metastasis resection in a unilateral dissection field ("template")

Adjuvant therapy with one cycle of cisplatin, etoposide and bleomycin

Intervention Type: DRUG

The patient is given the option for an adjuvant therapy with one cycle of cisplatin, etoposide and bleomycin two to four weeks after RA-RPLND

Interventions

Robot-assisted retroperitoneal lymph node dissection

Robot-assisted, if possibe ipsilateral nerve-sparing, retroperitoneal lymph node dissection and metastasis resection in a unilateral dissection field ("template")

Intervention Type: PROCEDURE

Adjuvant therapy with one cycle of cisplatin, etoposide and bleomycin

The patient is given the option for an adjuvant therapy with one cycle of cisplatin, etoposide and bleomycin two to four weeks after RA-RPLND

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed pure seminomatous testicular germ cell tumor
• Presence of iliac or retroperitoneal lymph node metastasis detected in contrast-enhanced CT or MRI, classified as local or unilaterally regional
• Maximum extent of lymph node metastasis (LN-M) singular or multiple, with a maximum size of 5 cm in transverse CT diameter (UICC IIB)
• Patients with an elevation in HCG after orchiectomy at the time of staging examination can be included if the directly preoperatively determined HCG does not exceed 5 IU/L.

Patients can be included in the following scenarios:

• Initial diagnosis of a tumor in UICC stage IIA/IIB
• Recurrence of a tumor in clinical stage (CS) I under active surveillance
• Recurrence of a CS I tumor after adjuvant therapy with carboplatin mono

Exclusion Criteria

• LN-M with a transverse diameter >5 cm in CT (UICC IIC)
• Other metastases than LN-M (UICC III)
• The patient received a different chemotherapy than described above
• The patient underwent retroperitoneal radiotherapy
• The patient is in a reduced general condition or has a life-threatening illness
• The patient has a psychiatric illness
• Evidence of non-seminomatous germ cell tumor components in the RPLND histology
• Complete resection cannot be ensured due to previous surgeries
• In the "high risk" group: Contraindications to cisplatin, etoposide, or bleomycin (severe liver insufficiency, severe kidney insufficiency, severe lung insufficiency, hypersensitivity, severe bone marrow depression, profound hearing impairments)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Heinrich-Heine University, Duesseldorf

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yue Che

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Düsseldorf

Locations

University Hospital of Duesseldorf

Düsseldorf, , Germany

Site Status: RECRUITING

Countries

Germany

Central Contacts

Yue Che

Role: CONTACT

yue.che@med.uni-duesseldorf.de

00492118118110

Facility Contacts

Yue Che

Role: primary

yue.che@med.uni-duesseldorf.de

Peter Albers

Role: backup

peter.albers@med.uni-duesseldorf.de

Other Identifiers

2022-2256

Identifier Type: -

Identifier Source: org_study_id