Clinical trial · Interventional
Precision Treatment of Recurrent/Metastatic Salivary Gland Carcinoma Guided by Molecular Typing
Cancer Hospital, Chinese Academy of Medical Sciences/National Cancer Center of China
NCT06145308CI-TRIAL-00107191recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Precision Therapy | — | UNRESOLVED | — |
| Salivary Gland Carcinoma | Salivary Gland Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (20)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| albumin-bound paclitaxel+trastuzumab+pyrotinib | Drug | — | UNRESOLVED |
| Albumin-paclitaxel + carboplatin + apatinib + camrelizumab | Drug | — | UNRESOLVED |
| Albumin-paclitaxel + platinum | Drug | — | UNRESOLVED |
| alpelisib+fulvestrant | Drug | — | UNRESOLVED |
| AR,AR antagonist +goserelin +docetaxel | Drug | — | UNRESOLVED |
| AR,AR antagonist ++ goserelin + pertuzumab + trastuzumab | Drug | — | UNRESOLVED |
| cadonilimab | Drug | — | UNRESOLVED |
| CDK4/6 inhibitor+AI or fulvestrant | Drug | — |
Design
Arms and outcomes
Arms (20)
- type
- EXPERIMENTAL
- label
- Cohort 1 (HER2-positive, RC48-ADC)
- description
- Disitamab vedotin 2.5 mg/kg will be administered as an intravenous infusion every 2 weeks (Q2W) as monotherapy, or in combination with physician-selected platinum-based chemotherapy (carboplatin 200-250 mg/m² IV Q2W or cisplatin 50 mg/m² IV Q2W).
- interventionNames
- Drug: Cohort 1 (HER2-positive, RC48-ADC)
- type
- EXPERIMENTAL
- label
- Cohort 2 (NTRK-fusion or NTRK-mutant)
- description
- larotrectinib 100 mg orally twice daily or entrectinib 600 mg orally once daily;
- interventionNames
- Drug: Cohort 2 (NTRK-fusion or NTRK-mutant)
- type
- EXPERIMENTAL
- label
- Cohort 3 (AR-positive, leuprolide + bicalutamide + abiraterone)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Inclusion Criteria:
* 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;
* Life expectancy is more than 3 months; ⑥Have at least one measurable lesion according to RECIST1.1 standards; ⑦Women of childbearing age must have a negative pregnancy test within 7 days before the first medication, and agree to receive the necessary contraceptive measures;
⑧The patient must have adequate liver, kidney, bone marrow, heart and lung and other organ functions:
⑨Understanding and voluntarily signing informed consent prior to performing any research-related evaluation/operation;
⑩Ability to comply with research visit schedules and other programmatic requirements.
Exclusion Criteria:
* 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;
* Major cardiovascular diseases;
* Is suffering from uncontrolled systemic diseases, including diabetes, hypertension, pulmonary fibrosis, acute lung disease, interstitial lung disease, cirrhosis, etc.;
* Is suffering from an active infection that requires systemic treatment;
* History of active tuberculosis; ⑨ Positive human immunodeficiency virus (HIV) test result; ⑩ Patients with chronic hepatitis B or active hepatitis C. ⑪Conditions that the investigator believes will affect the safety or compliance of the drug therapy in this study ⑫Female/male who is pregnant or breastfeeding or who intends to give birth;References
Publications (0)
Data not yet available
No reference posted for this study.