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Study identifier: NCT05705687 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Validation of a Treatment Algorithm for Poor-Risk NSGCTnon Seminomatous Germ-cell Tumors

Condition: Non-Seminomatous Germ Cell Tumor  ·  Sponsor: Gustave Roussy, Cancer Campus, Grand Paris

PhaseNA
Planned participants150
Who can joinMale, 16 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective multicenter, non-randomized research program that includes: * a phase IV study (for all patients) with a collection of tissue specimens of tumor, * a phase II study (for patients with primary mediastinal tumors and an unfavorable decline in tumor markers), * and a diagnostic study (for all patients, except patients with brain metastases at baseline or patients for whom any brain MRI is contra-indicated). The main question it aims to answer is improving outcome for young adults with poor-prognosis Non Seminomatous Germ Cell Tumor (NSGCT) is to validate prospectively the efficacy and safety of a personalized treatment based on early tumor marker kinetic assessment in real life for patients with poor-prognosis NSGCT. Participants will be followed-up according to the assessment of decline kinetics of the tumor markers at the end of a first chemotherapy cycle and according to the localisation of the primary lesion if unfavorable. * In the case of a patient with a favorable decline of the tumor markers, he will be treated by 3 additional standard chemotherapy cycles. * In the case of a patient with a testicular or peritoneal primary tumor and an unfavorable decline of the tumor markers, the patient will be treated by a dose-dense standard therapy. * The patient with a mediastinal primary tumor and an unfavorable decline of the tumor markers will be proposed to enter the phase II part of the study or to enter the dose-dense regimen like the other primary lo…

This description comes directly from the study's public registry record.

Talk to the study team

Elodie LECERF, MSc  ·  +33 (0)1 42 11 42 11  ·  elodie.lecerf@gustaveroussy.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Gustave RoussyVillejuif, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05705687