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Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Completed PHASE2 INTERVENTIONAL NCT01969578

Androgen Deprivation Therapy in Advanced Salivary Gland Cancer

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Salivary Gland (SG) Cancers are a rare and heterogeneous group of tumors, usually approached by multidisciplinary teams in high specialized centers. Until today no standard of care exists to treat these cancers. The identification of a target, the androgen receptor, in SG tumors has allowed for new treatment strategies options for this rare group of diseases. As a matter of fact, strong positivity for androgen expression has been found in salivary duct carcinoma and adenocarcinomas. The purpose of this study is therefore to evaluate the efficacy and safety of chemotherapy versus androgen deprivation therapy (ADT) in patients with recurrent and/or metastatic AR expressing SGCs. The study will include two cohorts of patients: Cohort A, which comprises chemo-naïve patients, and Cohort B, which comprises pretreated patients.

Detailed Description

Patients in Cohort A will be randomized 1:1 at the study entry to receive ADT (triptorelin + bicalutamide 50 mg) or standard chemotherapy. Patients of Cohort A randomized to the control arm (chemotherapy arm) will be given the option to enter Cohort B at the time of disease progression. As long as Cohort A is open to recruitment, patients who will be treated by chemotherapy will be simultaneously enrolled in Cohort B. Accrual in Cohort B will be stopped when recruitment of 76 eligible patients in Cohort A is reached.

Interventions

Name: bicalutamide + triptorelin
Type: DRUG
Description:
Name: Cisplatin + Doxorubicin
Type: DRUG
Description:
Name: Carboplatin + Paclitaxel
Type: DRUG
Description:

Primary Outcomes

Measure: Progression Free Survival (PFS)
TimeFrame: 37 months after First Patient In
Description: PFS is a primary outcome for cohort A
Measure: Response rate (RR)
TimeFrame: 37 months after First Patient In
Description: RR is a primary outcome for cohort B

Trial Information

NCT ID

NCT01969578

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

European Organisation for Research and Treatment of Cancer - EORTC

Last Updated

December 15, 2025