About this trial
Patients with salivary gland carcinoma were divided into groups according to HER2, NTRK, AR, TROP-2, etc. Patients in different groups were given precision targeted therapy or chemotherapy to evaluate the efficacy (ORR rate) and safety of precision therapy.
Eligibility criteria
Qualifiers
Patients with histopathologic diagnosis of salivary gland carcinoma
The tumor tissues were subjected to HER2/NTRK/AR/TROP-2 immunohistochemical staining.
ECOG physical status 0 or 1 score in the 3 days before the first medication of the study treatment;
Age 18 or older - no upper limit;
Disqualifiers
Known hypersensitivity or delayed anaphylaxis to any agents in this trial;
Major surgery had been performed within 4 weeks prior to the start of the study and did not fully recover;
Have received a live vaccine within 4 weeks before the start of the study or plan to receive any vaccine during the study period ;
To study the occurrence of arterial/venous thrombosis events within 6 months before medication;
Trial design
Treatments tested in this trial
- Cohort 1 (HER2-positive, RC48-ADC)
- Cohort 2 (NTRK-fusion or NTRK-mutant)
- Cohort 3 (AR-positive, leuprolide + bicalutamide + abiraterone)
- TROP2 ADC
- TKI
- Albumin-paclitaxel + platinum
- Albumin-paclitaxel + carboplatin + apatinib + camrelizumab
- albumin-bound paclitaxel+trastuzumab+pyrotinib
- HER2,trastuzumab deruxtecan± pertuzumab
- AR,AR antagonist ++ goserelin + pertuzumab + trastuzumab
- AR,AR antagonist +goserelin +docetaxel
- ivonescimab + investigator-choice platinum doublet+
- iparomlimab + tuvonralimab
- cadonilimab
- CDK4/6 inhibitor+AI or fulvestrant
- alpelisib+fulvestrant
- PARP inhibitor
- enfortumab vedotin
- HER2, pyrotinib + pertuzumab/trastuzumab
- vebecotutamab ±lenvatinib
Treatment groups
20
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Peking Union Medical College
Lead sponsor
Peking University Hospital of Stomatology
Collaborator