RO4929097 and Letrozole in Treating Post-Menopausal Women With Hormone Receptor-Positive Stage II or Stage III Breast Cancer
A Phase Ib Neoadjuvant Study of the Gamma Secretase Inhibitor (RO4929097) in Combination With the Aromatase Inhibitor Letrozole in Post-Menopausal Women With Stage II/III Hormone Receptor-Positive Breast Cancer
研究概览
地位
详细说明
PRIMARY OBJECTIVES:
I. To establish the maximum-tolerated dose and the recommended phase II dose of gamma-secretase inhibitor RO4929097 (RO4929097) in combination with letrozole in post-menopausal women with hormone receptor-positive stage II or III breast cancer.
II. To assess the safety of this regimen in these patients.
SECONDARY OBJECTIVES:
I. To evaluate the pharmacokinetics of this regimen, taking into consideration the induction of CYP3A4, in these patients.
II. To characterize the pharmacodynamic effects of letrozole prior to and during administration of RO4929097 with attention to suppression of estradiol and estrone levels.
III. To describe the pharmacodynamic effects of letrozole with or without RO4929097 on the NOTCH pathway, proliferation, angiogenesis, stromal cell infiltration/pathways, and comprehensive genomic analysis in tumor tissue of these patients.
IV. To describe the response, including clinical complete or partial objective response, pathological complete response, and attainment of pathologic stage 0 or I status in these patients.
OUTLINE: This is a multicenter, dose-escalation study of gamma-secretase inhibitor RO4929097(RO4929097).
Patients receive oral letrozole once daily on days 1-21. Beginning in course 2, patients also receive oral RO4929097 on days 1-3, 8-10, and 15-18. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.
Beginning 1 week after completion of neoadjuvant therapy, patients undergo surgery or tumor biopsy. Patients continue to receive oral letrozole once daily during surgery and for an additional 4 weeks.
Blood and tumor tissue samples are collected at baseline and periodically during study for pharmacokinetics, pharmacodynamics, and correlative studies.
After completion of study therapy, patients are followed up for 1 month and then every 6 months for 5 years.
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
学习地点
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Alabama
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Birmingham、Alabama、美国、35294
- University of Alabama at Birmingham
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Pennsylvania
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Pittsburgh、Pennsylvania、美国、15213
- Magee-Womens Hospital of UPMC
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Pittsburgh、Pennsylvania、美国、15232
- University of Pittsburgh Cancer Institute
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
Pathologically confirmed invasive breast cancer
Stage II or III disease (T2-T3, N0-2)
- No N3, T4 disease
Estrogen receptor-positive (ER+) and/or progesterone receptor-positive (PR+)
- H score ≥ 10 or positivity ≥ 10%
- HER2 negative as determined by IHC (1 or 2+) or FISH (< 2.0+)
- Bilateral disease allowed as long as all tumors are ER+ and ≥ 1 is T2-T3
Patient must have disease that is palpable on physical exam and able to be imaged via breast ultrasound
- Defined as ≥ 1 T2 tumor > 2 cm
- Multifocal disease allowed provided that ≥ 1 of the tumors is > 2 cm
- No metastatic disease by CT scans of the chest, abdomen, and pelvis, a PET/CT bone scan, or nuclear medicine bone scan
- No inflammatory breast cancer or presence of breast tumor cells in the dermal lymphatics of the breast
Post-menopausal meeting 1 of the following criteria:
- Bilateral oophorectomy
- Age ≥ 50 years and amenorrheic for > 12 months in the absence of chemotherapy, tamoxifen, toremifene, or ovarian suppression (spontaneous amenorrhea)
- ECOG performance status (PS) 0-2 (Karnofsky PS 60-100%)
- Life expectancy > 3 months
- ANC ≥ 1,000/mm³
- Platelet count ≥ 100,000/mm³
- Hemoglobin ≥ 9 g/dL
- Total bilirubin normal
- AST and ALT ≤ 2.5 times upper limit of normal
- Creatinine normal OR creatinine clearance ≥ 60 mL/min
- Baseline QTcF ≤ 470 msec
- No history of allergic reactions attributed to compounds of similar chemical or biologic composition to gamma secretase inhibitor RO4929097 or other agents used in the study
- No malabsorption syndrome or other condition that would interfere with intestinal absorption
- Able to swallow tablets
- Not serologically positive for hepatitis A, B, or C, or have a history of liver disease, other forms of hepatitis, or cirrhosis
- No uncontrolled electrolyte abnormalities including hypocalcemia, hypomagnesemia, hyponatremia, hypophosphatemia, or hypokalemia despite adequate electrolyte supplementation
No uncontrolled intercurrent illness including, but not limited to, any of the following:
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- History of torsades de pointes or other significant cardiac arrhythmia other than chronic, stable atrial fibrillation
- Psychiatric illness and/or social situations that would limit compliance with study requirements
- Recovered to < grade 2 CTCAE toxicities related to prior therapy
No prior chemotherapy, hormonal therapy, radiotherapy, or biological therapy for breast cancer
- Prior treatment for non-melanoma skin cancer or carcinoma in situ of the cervix allowed
- No prior hormone therapy for ductal carcinoma in situ (DCIS)
- No other concurrent investigational agents
- No concurrent medications with narrow therapeutic indices that are metabolized by cytochrome P450 (CYP450), including warfarin sodium (Coumadin®)
No concurrent medications that are strong inducers and/or inhibitors or substrates of CYP3A4
- Switching to alternative medications allowed
- No concurrent combination antiretroviral therapy for HIV-positive patients
- No concurrent antiarrhythmics or other medications known to prolong QTc
- No other concurrent anticancer agents or therapies
- No concurrent grapefruit juice
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Arm I
Patients receive oral letrozole once daily on days 1-21. Beginning in course 2, patients also receive oral RO4929097 on days 1-3, 8-10, and 15-18. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. Beginning 1 week after completion of neoadjuvant therapy, patients undergo surgery or tumor biopsy. Patients continue to receive oral letrozole once daily during surgery and for an additional 4 weeks. |
其他名称:
其他名称:
其他名称:
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
MTD defined as the dose level at which no more than 1 of 6 patients experience a DLT, and the dose below that at which at least 2/6 patients have DLT according to NCI CTCAE version 4.0
大体时间:21 days
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21 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
大体时间:Baseline
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
Baseline
|
|
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
大体时间:21 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
21 days
|
|
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
大体时间:42 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
42 days
|
|
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
大体时间:At time of surgery
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
At time of surgery
|
|
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
大体时间:Baseline
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
For the analysis of the gene expression data, the overall false discovery rate (FDR), which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
|
Baseline
|
|
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
大体时间:21 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
|
21 days
|
|
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
大体时间:42 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
|
42 days
|
|
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
大体时间:At time of surgery
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
|
At time of surgery
|
|
Measurement of cell proliferation (Ki-67)
大体时间:Baseline
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
Baseline
|
|
Measurement of cell proliferation (Ki-67)
大体时间:21 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
21 days
|
|
Measurement of cell proliferation (Ki-67)
大体时间:42 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
42 days
|
|
Measurement of cell proliferation (Ki-67)
大体时间:At time of surgery
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
At time of surgery
|
|
Measurement of appoptosis (TUNEL and activated caspase)
大体时间:Baseline
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
Baseline
|
|
Measurement of appoptosis (TUNEL and activated caspase)
大体时间:21 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
21 days
|
|
Measurement of appoptosis (TUNEL and activated caspase)
大体时间:42 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
42 days
|
|
Measurement of appoptosis (TUNEL and activated caspase)
大体时间:At time of surgery
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
At time of surgery
|
|
Measurement of angiogenesis (VEGF and CD31)
大体时间:Baseline
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
Baseline
|
|
Measurement of angiogenesis (VEGF and CD31)
大体时间:21 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
21 days
|
|
Measurement of angiogenesis (VEGF and CD31)
大体时间:42 days
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
42 days
|
|
Measurement of angiogenesis (VEGF and CD31)
大体时间:At time of surgery
|
All measurements are continuous.
Descriptive statistics will be calculated to summarize change of each measurement from the baseline value.
A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
|
At time of surgery
|
合作者和调查者
调查人员
- 首席研究员:Shannon Puhalla、University of Pittsburgh
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- NCI-2011-02487 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- U01CA099168 (美国 NIH 拨款/合同)
- UPCI-09-080
- CDR0000683397
- UPCI 09-080 (其他标识符:University of Pittsburgh Cancer Institute)
- 8554 (其他标识符:CTEP)
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