Study of SHR-A1811 Combined With Pyrotinib and Bevacizumab in Advanced Breast Cancer With Brain Metastasis

NCT ID: NCT06718933

Last Updated: 2025-02-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 74 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-01-08
• Study Completion Date: 2027-02-28

Brief Summary

In phase Ib, our study is aimed to evaluate the safety and tolerance of SHR-A1811 combined with pyrotinib in breast cancer with brain metastasis, and confirm the recommended phase 2 dose combined with preliminary results of efficacy.

In phase II, our study is aimed to evaluate the efficacy and safety of SHR-A1811 combined with pyrotinib and bevacizumab at RP2D in breast cancer with brain metastasis.

Conditions

Breast Cancer Metastatic; Breast Cancer Brain Metastases

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

SHR-A1811+pyrotinib

In phase Ib, enrolled subjects will received SHR-A1811 combined with pyrotinib at different doses to confirm RP2D and evaluate the safety and tolerance.

Group Type: EXPERIMENTAL

SHR-A1811

Intervention Type: DRUG

ADC

Pyrotinib

Intervention Type: DRUG

anti-HER2 inhibitor

SHR-A1811+pyrotinib+bevacizumab

In phase II, enrolled subjects will received SHR-A1811 combined with pyrotinib and bevacizumab to evaluate the efficacy and safety.

Group Type: EXPERIMENTAL

SHR-A1811

Intervention Type: DRUG

ADC

Bevacizumab

Intervention Type: DRUG

bevacizumab biosimilar

Pyrotinib

Intervention Type: DRUG

anti-HER2 inhibitor

Interventions

SHR-A1811

ADC

Intervention Type: DRUG

Bevacizumab

bevacizumab biosimilar

Intervention Type: DRUG

Pyrotinib

anti-HER2 inhibitor

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• More than 18 years old;
• ECOG PS Score: 0~2;
• Patients must have a life expectancy ≥ 3 months;
• Brian metastasis confirmed by MRI, at least one measurable brain lesion based on RANO-BM with no prior radiotherapy;
• Mannitol or hormone therapy is allowed to use for brain metastasis before enrolment, but treatment dosage should be stable for one week and not need to be increased;
• Adequate organ function and marrow function;
• Has recovered from any AEs (≤ grade 1) related to prior anti-tumour treatments before first dose of study therapy, except: a. alopecia; b. hyperpigmentation;
• Willing to join in this study, able to provide written informed consent, good compliance and willing to cooperate with follow-up.

Exclusion Criteria

• Has leptomeningeal metastasis or cystic metastatic lesions confirmed by MRI or lumbar puncture;
• Existence of third space fluid (e.g. massive ascites, pleural effusion, pericardial effusion) that is not well controlled by effective methods, e.g. drainage;
• Has CNS complications with the need for emergency intervention, or brain metastasis with poorly controlled symptoms by hormone or dehydration therapy, such as uncontrollable intracranial hypertension, mental disorder or epilepsy;
• Prior bevacizumab or EGFR-TKI is allowed, but should meet the following requirements at the same time:

1. No disease progression during prior bevacizumab or EGFR-TKI;

2. More than 3 months from the interruption of bevacizumab or EGFR-TKI to disease progression;

• Has received whole brain radiotherapy, chemotherapy, surgery within 2 weeks before first dose of study therapy; has received trastuzumab-based therapy or endocrine therapy within one week before first dose of study therapy; has received palliative radiotherapy for bone metastasis within 2 weeks before first dose of study therapy;
• Has known clinically significant lung disease, that is, moderate-to-severe lung disease which severely affects respiratory function, including but not limited to: idiopathic pulmonary fibrosis, pneumonitis. Prior ≥ grade 3 interstitial lung disease is not allowed to enrolment;
• Has received full-dose anticoagulants or thrombolytics within 10 days before enrolment, or non-steroid anti-inflammatory drugs with platelet inhibition (except low-dose aspirin (≤325mg qd) for preventive use);
• Existence of unhealed wound, active gastric ulcer, and other diseases which may cause haemorrhage risk (e.g., prior major operation within 4 weeks before enrolment, prior arterial or venous thrombotic event within one year before enrolment, prior cerebralvascular accident);
• Has known hereditary haemorrhagic tendency or coagulation disorder;
• Has joined in other clinical drug trials within 2 weeks before enrolment;
• Use of other antitumor systemic treatment during the study at the same time, except bisphosphonates for the treatment of bone metastasis or osteoporosis prevention;
• Other malignancy within prior 5 years unless curatively treated with no evidence of disease for at least recent 3 years, except: curatively treated in situ cancer of the cervix, skin basal cell carcinoma or skin squamous cell carcinoma;
• Cardiac insufficiency, including but not limited to: congestive heart failure, transmural myocardial infarction, angina which needs drug treatments, clinically significant valvulopathy and high-risk arrhythmia, or QTc abnormity with clinical significance in ECG examination during the screening period (corrected QTc >450 msec [male] or QTc >470 msec [female] under the resting state);
• Uncontrolled hypertension (under the resting state: systolic pressure >160mmHg or diastolic pressure >100mmHg);
• Other diseases which may affect study results, including but not limited to: 1) known history of immunodeficiency, including HIV-positive, other acquired or innate immunodeficient disease, or known history of organ transplantation; 2) HBsAg-positive and HBV DNA≥1000 IU/mL, or HCV antibody-positive, or treponema pallidum antibody-positive; 3) hypersensitivity to study therapy or any of its excipients; 4) severe infection requiring antibiotics, antiviral or antifungal treatment;
• Female patients during the gestation or suckling period, of childbearing potential and pregnancy test-positive, or unwilling to use an effective method of contraception during the whole study;
• Inability to swallow, intestinal obstruction or existence of other factors affecting medication and absorption;
• Any other conditions not appropriate for study enrolment in the opinion of the investigator.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Hongxia Wang

Chief physician

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Hongxia Wang, Chief physician

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Biyun Wang, Chief physician

Role: PRINCIPAL_INVESTIGATOR

Fudan University

Locations

Fudan Cancer Hospital

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Hongxia Wang, Chief physician

Role: CONTACT

whx365@126.com

+8621-38196379

Ting Li, Associate chief physician

Role: CONTACT

cinderellaliting@126.com

+86-18121299346

Facility Contacts

Hongxia Wang, Chief physician

Role: primary

whx365@126.com

+8621-38196379

Ting Li, Associate chief physician

Role: backup

cinderellaliting@126.com

+86-18121299346

Other Identifiers

BCBM-004

Identifier Type: -

Identifier Source: org_study_id