Choosing Neoadjuvant Chemotherapy Versus Hormonal Therapy for Breast Cancer Based on Gene Expression Profile

Virginia Commonwealth University8 个研究点分布在 2 个国家目标入组 59 人开始时间: 2011年4月最近更新: 2016年7月12日

适应症

干预措施

试验速览

阶段: 不适用
状态: 已完成
发起方: Virginia Commonwealth University
入组人数: 59
试验地点: 8
主要终点: The Proportion of Patients With RS 11-25 Who Refused the Assigned Treatment

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This randomized pilot clinical trial studied whether the Oncotype DX gene expression "Recurrence Score" (RS) would be useful for helping make a decision about which type of pre-operative treatment, hormone therapy or chemotherapy would be a better for patients with hormone responsive cancers that were not suitable for breast conserving surgery. The RS is currently used to predict the risk of distant recurrence and the benefit of the addition of chemotherapy to hormonal therapy in the adjuvant setting.

详细描述

Assessed the feasibility of carrying out a large-scale multi-center trial in which recurrence score (RS) was used to select treatment type in the neoadjuvant setting. Whether patients with intermediate RS were willing to be randomized between hormonal and chemotherapy.

The treatment received was not experimental and considered standard treatment for the type of cancer the participants had. What was experimental included the way in which they were assigned to a type of treatment. The design of this study was used to help determine if RS can be used to predict which type of treatment women with breast cancer are most likely to benefit from.

OUTLINE: Patients are assigned to 1 of 3 groups based on RS following Oncotype Dx gene expression profiling.

GROUP 1 (RS < 11): Patients receive neoadjuvant hormonal therapy comprising tamoxifen (pre-menopausal women) or an aromatase inhibitor (post-menopausal women) for 4-6 months in the absence of disease progression or unacceptable toxicity.
GROUP 2 (RS 11-25): Patients are randomized to 1 of 2 treatment arms:
ARM 1: Patients receive neoadjuvant hormonal therapy as in group I.
ARM 2: Patients receive 6-8 courses of neoadjuvant chemotherapy comprising an anthracycline/taxane based regimen over 4-6 months in the absence of disease progression or unacceptable toxicity.
GROUP 3 (RS > 25): Patients receive neoadjuvant chemotherapy as in group 2 arm 2.

研究设计

研究类型: Interventional
分配方式: 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 —（Adult, Older Adult）
性别: Female
接受健康志愿者: 否

入选标准

•The treating surgeon must determine that breast conservation therapy (BCT) would be made more feasible by reducing tumor size using neoadjuvant systemic therapy
•The patient must have signed and dated an institutional review board (IRB) approved consent form that conforms to federal and institutional guidelines
•The patient must be female
•The patient must be greater than or equal to 18 years old
•The patient must have an Eastern Cooperative Oncology Group Score (ECOG) performance status of 0 or 1
•The diagnosis of invasive carcinoma of the breast must have been made by core needle biopsy
•The primary breast tumor must be >= 2 cm by physical exam or imaging
•Ipsilateral axillary lymph nodes must be evaluated by imaging (MRI or ultrasound) within 6 weeks prior to randomization; If indicated for abnormal lymph nodes, fine needle aspirate (FNA) or core biopsy must be performed.
•The tumor must have been determined to be HER2-negative as follows:
•Fluorescent in situ hybridization (FISH)-negative (defined by ratio of HER2 to Chromosome 17 centromere (CEP17) must be < 2.2) or, if a ratio was not performed, the HER2 gene copy number must be < 4 per nucleus; or
•Chromogenic in situ hybridization (CISH) is performed, the result must indicate a HER2 gene copy number of < 6 per nucleus; or
•Immunohistochemistry (IHC) 0-1+; or
•IHC 2+ and FISH-negative or CISH-negative
•The tumor must have been determined to be ER+ and/or progesterone positive (PgR+) defined as > 10% tumor staining by immunohistochemistry
•The patient must have been evaluated by a treating physician, reviewed and discussed by the multi-disciplinary breast team, and considered to be a candidate for chemotherapy

排除标准

•FNA alone to diagnose the primary tumor
•Excisional biopsy or lumpectomy performed prior to randomization
•Surgical axillary staging procedure or sentinel node (SN) biopsy performed prior to registration
•Tumors clinically staged as including inflammatory breast cancer
•Ipsilateral cN2b or cN3 disease (patients with cN1 or cN2a disease are eligible)
•Definitive clinical or radiologic evidence of metastatic disease (Note: chest imaging [mandatory for all patients] and other imaging [if required] must have been performed within 6 weeks prior to randomization)
•Synchronous or metachronous contralateral invasive breast cancer; (patients with synchronous and/or metachronous contralateral ductal carcinoma in situ (DCIS) or lobular carcinoma in situ (LCIS) are eligible)
•HER2 test result of IHC 3+, regardless of FISH results, if performed
•Any history of ipsilateral invasive breast cancer or ipsilateral DCIS if treated with radiation therapy (RT); (patients with synchronous or metachronous ipsilateral LCIS are eligible)
•History of non-breast malignancies, except for in situ cancers treated only by local excision and basal cell and squamous cell carcinomas of the skin, within 5 years prior to randomization
•Treatment including RT, chemotherapy, and/or targeted therapy for the currently diagnosed breast cancer prior to registration
•Cardiac disease (history of and/or active disease) that would preclude the use of chemotherapy
•Pregnancy or lactation at the time of randomization; (Note: pregnancy testing must be performed within 2 weeks prior to randomization for women of childbearing potential)
•Other non-malignant systemic disease that would preclude the patient from receiving study treatment or would prevent required follow-up
•Psychiatric or addictive disorders or other conditions that, in the opinion of the investigator, would preclude the patient from meeting the study requirements
•Use of any investigational product within 30 days prior to registration

研究组 & 干预措施

Group 1 (RS < 11)

Experimental

Patients with a Recurrence Score (RS) less than 11 (RS <11) are assigned to Group 1, neoadjuvant hormonal therapy either tamoxifen (pre-menopausal women) or an aromatase inhibitor (post-menopausal women) for 4-6 months in the absence of disease progression or unacceptable toxicity.

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Neoadjuvant Therapy (Procedure)

Group 1 (RS < 11)

Experimental

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Therapeutic Conventional Surgery (Procedure)

Group 1 (RS < 11)

Experimental

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Laboratory Biomarker Analysis (Other)

Group 1 (RS < 11)

Experimental

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Gene Expression Analysis (Genetic)

Group 1 (RS < 11)

Experimental

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Tamoxifen Citrate (Drug)

Group 1 (RS < 11)

Experimental

Treatment:

Neoadjuvant therapy
Therapeutic conventional surgery
Laboratory biomarker analysis/Correlative studies
Gene Expression Analysis/ Oncotype DX Gene Expression Profiling System
Hormonal therapy:
Tamoxifen Citrate (pre-menopausal women) OR
Aromatase Inhibition Therapy (post-menopausal women)

干预措施: Aromatase Inhibition Therapy (Drug)