Clinical trial · Interventional
TOPAZ: Tucatinib in COmbination With Pembrolizumab And TrastuZumab in Patients With HER2-Positive Breast Cancer Brain Metastases
TOPAZ: Single Arm, Open Label Phase 1b/2 Study of Tucatinib in COmbination With Pembrolizumab And TrastuZumab in Patients With HER2-Positive Breast Cancer Brain Metastases
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Study withdrawn due to change in treatment landscape for HER2+ metastatic breast cancer.
Summary
Brief summary (as posted)
This is a single arm, open label trial to assess the safety and efficacy of tucatinib in combination with pembrolizumab and trastuzumab for the treatment of HER2+ breast cancer brain metastases (BCBM). A total of 33 patients with untreated or previously treated and progressing HER2+ BCBM not requiring urgent central nervous system (CNS)-directed therapy will be enrolled. The study will determine the recommended dose of tucatinib in this combination and assess the efficacy of this combination in controlling CNS disease in patients with HER2+ BCBM.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain Metastases | — | UNRESOLVED | — |
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| CNS Disease | — | UNRESOLVED | — |
| HER2-positive Breast Cancer | HER2-Positive Breast Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pembrolizumab | Drug | Pembrolizumab | ALIAS |
| Trastuzumab | Drug | Trastuzumab | ALIAS |
| Tucatinib | Drug | Tucatinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Tucatinib + Pembrolizumab + Trastuzumab
- description
- Patients will receive a combination therapy of tucatinib with pembrolizumab and trastuzumab during the treatment period until progression, treatment intolerance, or patient withdrawal from study. Tucatinib and pembrolizumab are administered as experimental use while trastuzumab is administered per standard use. Patients are expected to be on treatment for at least 12 weeks.
- interventionNames
- Drug: Tucatinib
- Drug: Pembrolizumab
- Drug: Trastuzumab
Primary outcomes (2)
- measure
- 24-week CNS disease control rate (DCR)
- timeFrame
- 24 weeks
- description
- Percentage of patients who experience objective tumor response \[ partial response (PR) or complete response (CR) \] or stable disease as assessed by investigator per RANO-BM reads on protocol-specified MRIs of the brain.
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age ≥18 years. 2. ECOG performance status of 0-2. 3. HER2+ (as defined by ASCO/CAP clinical practice guideline) metastatic breast cancer. 4. Untreated or previously treated and progressing CNS disease. 5. Measurable CNS metastases. 6. Must be able to undergo MRI of the brain. 7. Adequate organ function. Exclusion Criteria: 1. Any indication for immediate CNS-directed therapy. 2. History of generalized or complex partial seizures. 3. Any other manifestation of neurologic progression that in the opinion of the treating physician is due to brain metastases. 4. Leptomeningeal disease. 5. Prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor. 6. Prior therapy with tucatinib. 7. Active autoimmune disease that has required systemic treatment in excess of prednisone 10mg daily or equivalent in the past 2 years. Complete inclusion/exclusion criteria are detailed in the protocol.
References
Publications (0)
Data not yet available