Clinical trial · Interventional
A Phase II Study of SHR-A1811 Combined With Radiotherapy in HER2-positive and HER2-low Breast Cancer Brain Metastases
SHR-A1811 Combined With Radiotherapy in HER2-positive and HER2-low Breast Cancer Brain Metastases: a Prospective,Sigle-arm,Phase II Study
NCT06975462CI-TRIAL-00089792not yet recruitingPhase 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)
A prospective, single-arm study to explore the efficacy and safety of SHR-A1811 combined with radiotherapy in patients with HER2-positive or HER2-low brain metastases
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer Metastatic | Breast Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SHR-A1811 and radiotherapy | Combination Product | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- SHR-A1811+radiotherapy
- description
- SHR-A1811:4.8mg/kg radiotherapy:800cGY\*5
- interventionNames
- Combination Product: SHR-A1811 and radiotherapy
Primary outcomes (1)
- measure
- The objective response rate of intracranial(IC-ORR)
- timeFrame
- 2 years
- description
- Proportion of participants with a complete response (CR) or partial response (PR) for intracranial tumors
Secondary outcomes (4)
- measure
- Intracranial CNS Progression Free Survival(IC-PFS)
- timeFrame
- 2 years
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Pathologically confirmed HER2 positive (IHC 3+ or IHC 2+/FISH+)or HER2-low(IHC1+ or 2+/FISH-) advanced breast cancer 2. Age\>18 years. 3. newly diagnosed Brain metastases confirmed by enhanced brain MRI. Metastases number less than 6. 4. No more than four lines of previous advanced therapy 5. Life expectancy of more than 3 months 6. There were no known or suspected leptomeningeal brain metastases 7. The interval from previous therapy was more than 2 weeks, and acute toxicity from previous therapy had to resolve to grade 1 or less 8. The use of mannitol, bevacizumab, or hormone therapy was allowed before enrollment, but the dose was stable for at least a week without the need for an increment 9. Screening laboratory values must meet the following criteria( and should be obtained within 28 days prior to registration): Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L, Platelets≥ 90 x 109/L, Hemoglobin ≥ 90 g/L Aspartate aminotransferase/alanine aminotransferase (AST/ALT) ≤2.5 x ULN without liver metastasis,≤ 5 x ULN with liver metastases Serum BUN and creatinine ≤ 1.5 x Upper Limit of Normal (ULN) LVEF ≥ 50% QTcF \< 480 ms INR≤1.5×ULN,APTT≤1.5×ULN 10.Signed the informed consent form prior to patient entry Exclusion Criteria: 1. Leptomeningeal or hemorrhagic metastases 2. previously used T-dxd 3. Uncontrolled epilepsy 4. Severe or uncontrolled disease: severe cardiovascular disease, end-stage renal disease, severe hepatic disease, history of immunodeficiency, including HIV positive, active HBV/HCV or other acquired congenital immunodeficiency disease, or organ transplantation history, active infection, etc. 5. History of allergy to treatment regimens 6. Pregnancy or lactation period, women of child-bearing age who are unwilling to accept contraceptive measures. 7. Inability to complete enhanced MRI 8. Not suitable for inclusion for specific reasons judged by sponsor -
References
Publications (0)
Data not yet available
No reference posted for this study.