Precise Targeted Therapy for Refractory HER2 Positive Advanced Breast Cancer Based on Genome Signature and Drug Sensitivity of PDO Model
试验速览
- 阶段
- 3 期
- 入组人数
- 120
- 试验地点
- 2
- 主要终点
- ORR
研究概览
简要总结
This is an open, prospective and interventional clinical study. Patients with advanced Human Epidermal Growth Factor Receptor 2 (HER2) positive breast cancer resistant to trastuzumab will be enrolled in the study. Histological specimens obtained from different metastatic foci of patients, are used to conduct genome-wide sequencing together with Circulating tumor DNA (ctDNA) of blood samples. Meanwhile, investigator will construct PDO model based on biopsy tissue. Patients as well as their paired Patient-derived organoids (PDO) models are divided into six groups according to genomic signatures. Each group of patients will receive the best targeted treatment scheme from the current clinical perspective, while the matched PDO model will accept a variety of potential effective schemes intervention. The future treatment plan of patients will be timely adjusted based on the tumor inhibition rate of PDO models. This study is the first time to explore the best individualized application sequence of targeted therapy for refractory HER2 positive breast cancer by combining genome sequencing with drug sensitivity test of PDO model. The results are expected to improve the prognosis of patients with advanced HER2 positive breast cancer.
详细描述
In previous studies, investigator found that dynamic genomics detection of metastatic foci can fully reveal the mechanism of trastuzumab resistance. Different anti-HER2 treatment strategies for different mechanisms can improve the efficacy of HER2 positive advanced breast cancer, and the PDO drug sensitivity test model of breast cancer can be prior to patients' response to the exact efficacy of specific regimens.This study aimed to explore the optimal individualized drug combination and order for patients with advanced HER2 positive breast cancer resistant to trastuzumab based on a variety of existing diagnosis and treatment methods. This is an open, prospective and interventional clinical study. Patients with advanced HER2 positive breast cancer resistant to trastuzumab will be enrolled in the study. Histological specimens obtained from different metastatic foci of patients, are used to conduct genome-wide sequencing together with ctDNA of blood samples. Meanwhile, investigator will construct PDO model based on biopsy tissue. Patients as well as their paired PDO models are divided into six groups according to genomic signatures. Each group of patients will receive the best targeted treatment scheme from the current clinical perspective, while the matched PDO model will accept a variety of potential effective schemes intervention. The future treatment plan of patients will be timely adjusted based on the tumor inhibition rate of PDO models. This study is the first time to explore the best individualized application sequence of targeted therapy for refractory HER2 positive breast cancer by combining genome sequencing with drug sensitivity test of PDO model. The results are expected to improve the prognosis of patients with advanced HER2 positive breast cancer.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •18-70 years old;
- •ECOG score 0-2;
- •Locally advanced or metastatic breast cancer confirmed by histopathology;
- •Positive HER2 expression in cancer tissues (IHC 3 +, or IHC 2 + but FISH amplification);
- •Resistant to trastuzumab (including disease progression during or after withdrawal of trastuzumab);
- •There were enough specimens for immunohistochemistry, gene detection and establishment of PDO model;
- •Hematology and liver and kidney function were normal within 2 weeks before treatment;
- •Imaging examination showed measurable lesions (according to RECIST v1.1);
- •Women of childbearing age agree to contraception or take contraceptive measures;
- •Be able to understand the research program and participate voluntarily.
排除标准
- •Symptomatic, untreated or progressive central nervous system metastases;
- •Severe heart disease (poor cardiac function);
- •Within 5 years, there was a history of other malignant tumors other than breast cancer;
- •In this study, chemotherapy, radiotherapy, immunotherapy or surgery were performed within 3 weeks before the first treatment;
- •Patients who are pregnant or lactating, or plan to become pregnant during enrollment.
研究组 & 干预措施
A. HER2 low expression
Phenotype was signatured by HER2 low expression.
干预措施: Trastuzumab (Drug)
A. HER2 low expression
Phenotype was signatured by HER2 low expression.
干预措施: Pertuzumab (Drug)
A. HER2 low expression
Phenotype was signatured by HER2 low expression.
干预措施: Nab paclitaxel (Drug)
B. HER2 amplified
Signatured by wild type HER2 amplified.
干预措施: Trastuzumab (Drug)
B. HER2 amplified
Signatured by wild type HER2 amplified.
干预措施: Pertuzumab (Drug)
B. HER2 amplified
Signatured by wild type HER2 amplified.
干预措施: Nab paclitaxel (Drug)
C. HER2 mutation
Signatured by HER2 mutation.
干预措施: Pyrotinib (Drug)
C. HER2 mutation
Signatured by HER2 mutation.
干预措施: Capecitabine (Drug)
D. HER2 downstream mutation
Signatured by HER2 downstream mutation of PI3KCA, TP53 or PTEN.
干预措施: Trastuzumab (Drug)
D. HER2 downstream mutation
Signatured by HER2 downstream mutation of PI3KCA, TP53 or PTEN.
干预措施: Nab paclitaxel (Drug)
D. HER2 downstream mutation
Signatured by HER2 downstream mutation of PI3KCA, TP53 or PTEN.
干预措施: T-DM1 (Drug)
D. HER2 downstream mutation
Signatured by HER2 downstream mutation of PI3KCA, TP53 or PTEN.
干预措施: Everolimus (Drug)
E. Hormone receptor pathway activation
Signatured by both ER and PR strongly expressed,or CCND1 amplified.
干预措施: Trastuzumab (Drug)
E. Hormone receptor pathway activation
Signatured by both ER and PR strongly expressed,or CCND1 amplified.
干预措施: CDK4/6 inhibitor (Drug)
E. Hormone receptor pathway activation
Signatured by both ER and PR strongly expressed,or CCND1 amplified.
干预措施: AI (Drug)
F. Immune activation
Signatured by high TMB or PD-L1 positively expressed.
干预措施: Trastuzumab (Drug)
F. Immune activation
Signatured by high TMB or PD-L1 positively expressed.
干预措施: Anti-PD-1 monoclonal antibody (Drug)
结局指标
主要结局
ORR
时间窗: Up to six weeks, first evaluation
objective response rate (ORR) according to RECIST (version 1.1) of each group
PDO model inhibition rate
时间窗: during the procedure
Tumor regression rate based on the calculation of the long diameter in each group
次要结局
- PFS1(during the procedure)
