PRIMETEST II - Phase II Trial to Prospectively Test New Predictors for Recurrence in Patients With Clinical Stage II A/B Seminoma Treated With RA-RPLND

Status: Recruiting
Location: See location...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Germany
University Hospital of Duesseldorf
RECRUITING
Düsseldorf
Contact Information
Primary
Yue Che
yue.che@med.uni-duesseldorf.de
00492118118110
Time Frame
Start Date: 2023-08-28
Estimated Completion Date: 2029-08-31
Participants
Target number of participants: 60
Treatments
Experimental: Low risk
Criteria for low risk:~* Absence of high risk criteria~* Previous carboplatin therapy post orchiectomy~* Exclusion of malignancy in the RPLND histology
Experimental: 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
Related Therapeutic Areas
Sponsors
Leads: Heinrich-Heine University, Duesseldorf

This content was sourced from clinicaltrials.gov