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Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases

Primary Purpose

Metastatic Breast Cancer

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
SHR-A1811
Pyrotinib
Bevacizumab
Sponsored by
Henan Cancer Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Breast Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Females ≥18 yrs old; Pathologically confirmed HER2-positive or HER2-low advanced breast cancer; At least one measurable intracranial lesion according to RANO-BM criteria, which had not received local treatment; Without prior cranial radiation and had no indication for immediate local treatment or refuse to local treatment; More than 2 weeks from last systemic treatment; patients with new brain lesions after craniocerebral surgery were admitted if no radiotherapy was performed. Patients with HER2-Low disease must not have systemic treatment for brain metastases. Prior HER2-target treatment, endocrine therapy and chemotherapy was allowed; Life expectancy is not less than 6 months. Adequate function of major organs. Exclusion Criteria: Leptomeningeal involvement; CNS complications requiring emergency neurosurgical intervention (e.g. excision, shunt tube placement);or uncontrolled symptomatic brain metastases; Previous treatment with trastuzumab deruxtecan (DS-8201a) or any other antibody drug conjugate (ADC) which consists of an exatecan derivative that is a topoisomerase 1 inhibitor; Patients who had progressed on previous HER2 tyrosine kinase inhibitor therapy were excluded from Arm 2, and those who had progressed on previous bevacizumab therapy were excluded from Arm 3; No concurrent antitumor therapy for metastatic cancer other than the study treatment; Antitumor radiotherapy, chemotherapy, surgery, targeted therapy, or immunotherapy within 2 weeks or endocrine therapy within 1 week prior to enrolment; Participated in other drug clinical trials within 4 weeks before admission; History of clinically significant lung disease; Other malignant tumors, excluding cured cervical carcinoma in situ, skin basal cell carcinoma or skin squamous cell carcinoma, have been diagnosed in the past five years. According to the judgement of the researchers, there are concomitant diseases that seriously endanger the safety of patients or affect the completion of research (including, but not limited to, severe hypertension, severe diabetes, active infections, etc.). Any other conditions that researchers believe that patients are unsuitable for this study.

Sites / Locations

  • Henan Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Arm 1

Arm 2

Arm 3

Arm 4

Arm Description

HER2-positive: SHR-A1811

HER2-positive: SHR-A1811 and pyrotinib

HER2-positive: SHR-A1811 and bevacizumab

HER2-low: SHR-A1811

Outcomes

Primary Outcome Measures

CNS-ORR by investigator
CNS-ORR was defined as percentage of participants with CNS response assessed by the investigator according to RANO-BM criteria

Secondary Outcome Measures

ORR by investigator using RECIST Guideline (Version 1.1)
ORR was defined as percentage of participants with best (confirmed) overall response (BOR) of either CR or PR assessed by the investigator according to RECIST version 1.1
PFS
PFS was defined as the time from first dose to first documented disease progression (PD) or death from any cause, whichever occurred first
Adverse events
Proportion of participants experienced adverse events during the study period

Full Information

First Posted
March 2, 2023
Last Updated
October 17, 2023
Sponsor
Henan Cancer Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05769010
Brief Title
Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases
Official Title
A Prospective, Open-label Explorative Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 31, 2023 (Actual)
Primary Completion Date
October 30, 2025 (Anticipated)
Study Completion Date
April 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Henan Cancer Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aimed to evaluate the use of SHR-A1811 in HER2-expression Advanced Breast Cancer patients with brain metastases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Breast Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
HER2-positive: SHR-A1811
Arm Title
Arm 2
Arm Type
Experimental
Arm Description
HER2-positive: SHR-A1811 and pyrotinib
Arm Title
Arm 3
Arm Type
Experimental
Arm Description
HER2-positive: SHR-A1811 and bevacizumab
Arm Title
Arm 4
Arm Type
Experimental
Arm Description
HER2-low: SHR-A1811
Intervention Type
Drug
Intervention Name(s)
SHR-A1811
Intervention Description
SHR-A1811: intravenous
Intervention Type
Drug
Intervention Name(s)
Pyrotinib
Intervention Description
Pyrotinib: oral
Intervention Type
Drug
Intervention Name(s)
Bevacizumab
Intervention Description
Bevacizumab: intravenous
Primary Outcome Measure Information:
Title
CNS-ORR by investigator
Description
CNS-ORR was defined as percentage of participants with CNS response assessed by the investigator according to RANO-BM criteria
Time Frame
2 months
Secondary Outcome Measure Information:
Title
ORR by investigator using RECIST Guideline (Version 1.1)
Description
ORR was defined as percentage of participants with best (confirmed) overall response (BOR) of either CR or PR assessed by the investigator according to RECIST version 1.1
Time Frame
2 months
Title
PFS
Description
PFS was defined as the time from first dose to first documented disease progression (PD) or death from any cause, whichever occurred first
Time Frame
up to 1.5 years
Title
Adverse events
Description
Proportion of participants experienced adverse events during the study period
Time Frame
up to 1.5 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Females ≥18 yrs old; Pathologically confirmed HER2-positive or HER2-low advanced breast cancer; At least one measurable intracranial lesion according to RANO-BM criteria, which had not received local treatment; Without prior cranial radiation and had no indication for immediate local treatment or refuse to local treatment; More than 2 weeks from last systemic treatment; patients with new brain lesions after craniocerebral surgery were admitted if no radiotherapy was performed. Patients with HER2-Low disease must not have systemic treatment for brain metastases. Prior HER2-target treatment, endocrine therapy and chemotherapy was allowed; Life expectancy is not less than 6 months. Adequate function of major organs. Exclusion Criteria: Leptomeningeal involvement; CNS complications requiring emergency neurosurgical intervention (e.g. excision, shunt tube placement);or uncontrolled symptomatic brain metastases; Previous treatment with trastuzumab deruxtecan (DS-8201a) or any other antibody drug conjugate (ADC) which consists of an exatecan derivative that is a topoisomerase 1 inhibitor; Patients who had progressed on previous HER2 tyrosine kinase inhibitor therapy were excluded from Arm 2, and those who had progressed on previous bevacizumab therapy were excluded from Arm 3; No concurrent antitumor therapy for metastatic cancer other than the study treatment; Antitumor radiotherapy, chemotherapy, surgery, targeted therapy, or immunotherapy within 2 weeks or endocrine therapy within 1 week prior to enrolment; Participated in other drug clinical trials within 4 weeks before admission; History of clinically significant lung disease; Other malignant tumors, excluding cured cervical carcinoma in situ, skin basal cell carcinoma or skin squamous cell carcinoma, have been diagnosed in the past five years. According to the judgement of the researchers, there are concomitant diseases that seriously endanger the safety of patients or affect the completion of research (including, but not limited to, severe hypertension, severe diabetes, active infections, etc.). Any other conditions that researchers believe that patients are unsuitable for this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Min Yan, Professor
Phone
+86 15713857388
Email
ym200678@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
HuiMin Lv
Phone
+86 15937162120
Email
lvhuimin999@163.com
Facility Information:
Facility Name
Henan Cancer Hospital
City
Zhengzhou
State/Province
Henan
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Yan, Professor
Phone
+86 15713857388
Email
ym200678@126.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Study of SHR-A1811 in HER2-expression Advanced Breast Cancer With Brain Metastases

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