SHR-A1921 Combined With Bevacizumab in Triple-negative Breast Cancer With Brain Metastases

Phase 2

Not yet recruiting

• Conditions: TNBC; Brain Metastasis
• Interventions: Drug: SHR-A1921 + Bevacizumab

• Registration Number: NCT06210438
• Lead Sponsor: Fudan University

Brief Summary

This is a phaseⅡ, single-arm study evaluating the efficacy and safety of SHR-A1921 Combined with Bevacizumab in Triple-negative Breast Cancer with Brain Metastases

Detailed Description

Not available

Study Timeline

• Status Verified: 2023-12
• Study First Submitted: 2024-01-04
• Study First Submitted QC: 2024-01-17
• Last Update Submitted: 2024-01-17
• Study First Posted: 2024-01-18
• Last Update Posted: 2024-01-18
• Study Start: 2024-02-01
• Primary Completion: 2025-06-30
• Study Completion: 2026-06-30

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

1. Age ≥ 18 years old, both genders

2. ECOG Performance Status of 0-2

3. Pathological tests confirm HR-negative/HER2-negative breast cancer；there is evidence of local recurrence or metastasis；not suitable with curative surgery or radiation therapy；HR negative is defined as: ER-negative and PR-negative, the proportion of positively stained tumor cells in all tumor cells is <10%；HER2- negative is defined as: histologically confirmed to be HER2 IHC (0) or HER2 IHC(1+) or HER2 IHC (2+) and FISH(-)

4. Must have life-expectancy of ≥ 3 months

5. MRI confirmed brain metastases, at least one intracranial parenchymal metastatic lesion with a longest diameter ≥ 1.0 cm without prior radiotherapy；

6. Intraventricular catheter shunting or mannitol、steroid hormone、anticonvulsant drug is allowed before enrollment, but the dose of drug should be stable for at least one week and the neurological symptoms are stable for ≥1 week

7. Adequate function of major organs meets the following requirements (1)Blood routine

   • ANC≥1.5×109/L；
   • PLT≥75×109/L；
   • Hb≥90 g/L(Allows blood transfusion or the use of medication to ensure that the content of hemoglobin) (2)Coagulation
   • INR≤1.5，APTT≤1.5×ULN (3)Blood biochemistry
   • TBIL≤1.5 × ULN;
   • ALT and AST≤3 × ULN (liver metastasis≤5.0 × ULN);
   • Urea nitrogen ≤ 1.5 × ULN; Cr≤1.5 × ULN or creatinine clearance ≥50 mL / min (Cockcroft-Gault formula) (4)Cardiac ultrasound
   • LVEF≥50%; (5)12-lead ECG:
   • females QTcF interval <470msec and males <450ms;

8. Willing to join the study, sign informed consent, have good compliance and cooperate with follow-up.

Exclusion Criteria

1. Leptomeningeal or cystic metastases confirmed by MRI or lumbar puncture
2. Presence of third interstitial fluid that cannot be controlled by drainage or other methods (e.g., a large amount of pleural effusion and ascites);
3. Whole brain radiotherapy, chemotherapy, biological targeted therapy, immunotherapy, surgery or endocrine therapy within 2 weeks prior to enrolment
4. Has received prior therapy with bevacizumab and TROP-2 ADC drugs
5. Participation in any other clinical trials within 2 weeks of enrollment
6. Concurrent use of any other Anti-cancer drugs
7. Other malignancies within 5 years, except cured in-situ of uterine cervix carcinoma , skin basal cell carcinoma and squamous-cell carcinoma
8. History of heart disease: (1) Arrhythmias requiring medical treatment or clinical significance, (2) Myocardial infarction, (3) Heart failure, (4)Any heart diseases that investigator believes not suitable for this study
9. History of allergy or hypersensitivity to any of the study drugs or study drug components
10. History of immunodeficiency including HIV-positive, active hepatitis B/C, other acquired, congenital immunodeficiency disease or history of organ transplantation
11. A clear history of neurological or mental disorders, including epilepsy or dementia
12. Pregnant or breastfeeding women. Women of childbearing potential who have a positive pregnancy test or unwilling to use adequate contraception prior to enrollment and for the duration of study participation
13. According to the investigator's judgment, there is a concomitant disease that seriously endangers the safety of subjects or affects the completion of the study (including but not limited to severe hypertension, severe diabetes, active infection, thyroid disease that cannot be controlled by drugs)
14. Any condition which in the investigator's opinion makes the subjects unsuitable for the study participation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
SHR-A1921 + Bevacizumab	SHR-A1921 + Bevacizumab	-

Primary Outcome Measures

Name	Time	Method
CNS ORR	from enrollment to progression or death (for any reason), assessed up to 24 months	The proportion of patients who have a CR or PR in the CNS, as determined by the Investigator according to RANO-BM criteria

Secondary Outcome Measures

Name	Time	Method
CNS CBR	from enrollment to progression or death (for any reason), assessed up to 24 months	CNS clinical benefit rate (CBR) will be defined as the percentage of patients who experience a CR, PR or Stable Disease (SD) for at least 24 weeks.
Safety as assessed by percentage of patients with any Adverse Event	Up to 2 years	Adverse event according to NCI-CTC AE 5.0
Overall survival	Up to 2 years	OS will be defined as the time from the first dose of treatment to death for any cause
First progression site	Up to 2 years	The first lesion to progress
Progression-free survival	Up to 2 years	PFS will be defined as the time from the first dose of treatment to death or disease progression

Trial Locations

Locations (1)

Fudan University Shanghai Cancer Center; 🇨🇳 Shanghai, Shanghai, China