This is a Phase 2, open-label, multi-center study of BGB-290 administered orally (PO) twice daily (BID) in adult Chinese patients with advanced HER2(-) breast cancer harboring germline BRCA mutation, which have progressed despite standard therapy, or for which no standard therapy exists.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
88
Administered orally
Cancer Hospital Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
Objective Response Rate (ORR) as Assessed by Independent Radiology Review (IRC)
ORR is defined as the percentage of participants who achieved a best overall response of confirmed complete response (CR) or partial response (PR), assessed by IRC per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
Time frame: From the first dose of pamiparib to first documentation of disease progression while participant is alive (Approximately 2 years and 4 months)
ORR as Assessed by Investigator
ORR is defined as the percentage of participants who achieved a best overall response of confirmed complete response (CR) or partial response (PR), assessed by the investigator per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
Time frame: From the first dose of pamiparib to first documentation of disease progression while participant is alive (Approximately 2 years and 10 months)
Progression-free Survival (PFS) as Assessed by IRC and Investigator
PFS is defined as the time from first dose of pamiparib to the first documented disease progression or death due to any cause, assessed by IRC or the investigator
Time frame: From the first dose of pamiparib to first documentation of disease progression or death (Approximately 2 years and 10 months)
Duration of Response (DOR) as Assessed by IRC
DOR is defined as the time from first determination of a confirmed best overall response until the first documentation of progression or death, whichever comes first, assessed by IRC
Time frame: From first documentation of confirmed CR or PR to first documentation of disease progression or death (Approximately 2 years and 10 months)
Duration of Response (DOR) as Assessed by the Investigator
DOR is defined as the time from first determination of a confirmed best overall response until the first documentation of progression or death, whichever comes first, assessed by the investigator
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Fujian Medical University Union Hospital
Fuzhou, Fujian, China
Sun Yat Sen Memorial Hospital, Sun Yat Sen University (North)
Guangzhou, Guangdong, China
Sun Yat Sen University Cancer Center
Guangzhou, Guangdong, China
Harbin Medical University Cancer Hospital
Harbin, Heilongjiang, China
Henan Cancer Hospital
Zhengzhou, Henan, China
Zhongnan Hospital of Wuhan University Wuhan
Wuhan, Hubei, China
Xiangya Hospital of Central South University
Changsha, Hunan, China
Hunan Cancer Hospital
Changsha, Hunan, China
Jiangsu Province Cancer Hospital
Nanjing, Jiangsu, China
...and 10 more locations
Time frame: From first documentation of confirmed CR or PR to first documentation of disease progression or death (Approximately 2 years and 10 months)
Confirmed Best Overall Response (BOR) as Assessed by IRC and Investigator
BOR is defined as the percentage of participants with best overall response recorded from the start of the treatment until disease progression or recurrence, assessed by IRC or the investigator. BOR included complete response \[CR\], partial response \[PR\], stable disease \[SD\], disease progression and not evaluable \[NE\].
Time frame: Approximately 2 years and 10 months
Disease Control Rate (DCR) as Assessed by IRC and Investigator
DCR is defined as the percentage of participants who achieved a confirmed BOR of CR, PR, or stable disease (SD), assessed by IRC or the investigator
Time frame: From the first dose of pamiparib to first documentation of disease progression while participant is alive (Approximately 2 years and 10 months).
Clinical Benefit Rate (CBR) as Assessed by IRC and Investigator
CBR is defined as percentage of participants with confirmed CR or confirmed PR or a durable SD (SD lasting ≥ 24 weeks), assessed by IRC or the investigator
Time frame: From the first dose of pamiparib to first documentation of disease progression while participant is alive (Approximately 2 years and 10 months)
Overall Survival (OS)
OS is defined as time from the first dose of pamiparib to the date of death due to any cause
Time frame: From the first dose of pamiparib until death (approximately 2 years and 10 months)
Number of Participants With Treatment-Emergent Adverse Events (TEAE) and Serious Adverse Events (SAE)
A TEAE is defined as an adverse event (AE) that had an onset date on or after the first dose of study drug up to 30 days following study drug discontinuation. SAE is defined as any AE that leads to death or is life-threatening.
Time frame: Up to approximately 2 years and 10 months