Clinical Trials Logo

Clinical Trial Summary

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, etc.) and safety of precision neoadjuvant or conversion therapy.


Clinical Trial Description

1. Patients with locally advanced/recurrent or oligometastatic 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, etc.) and safety of precision neoadjuvant or conversion therapy. 2. Patients with locally advanced/recurrent or metastatic salivary gland carcinoma with symptoms and rapid progression who could not tolerate or refuse surgery were divided into groups according to HER2, NTRK, AR, TROP-2, etc. Patients in different groups were given precise targeted therapy or chemotherapy to evaluate the efficacy (ORR rate, etc.) and safety of rescue therapy. 3. To explore biomarkers related to the efficacy of precision treatment of salivary gland cancer. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06145308
Study type Interventional
Source Peking Union Medical College
Contact fei Ma
Phone 13910217780
Email drmafei@126.com
Status Recruiting
Phase Phase 2
Start date May 1, 2024
Completion date July 10, 2026