Predicting Response and Toxicity in Patients Receiving Paclitaxel and Avastin for Breast Cancer

NCT ID: NCT00537173

Last Updated: 2017-01-25

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 11 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2007-09-30
• Study Completion Date: 2009-08-31

Brief Summary

This trial provides a unique opportunity in that it combines genomic, proteomic and pharmacogenomic assessments in patients receiving chemotherapy for advanced breast cancer. To date no other trials have analyzed gene and protein expression at the same time points in the same patient, combined with clinical outcome. Similar to previous attempts to predict response based on expression of a single gene or protein, we expect that neither genomic or proteomic profiling alone will be sufficient to optimize therapy. Rather, we expect an iterative process that combines information gleaned from both platforms, modified to avoid toxicity based on pharmacogenomics.

Detailed Description

OUTLINE: This is a multi-center study.

Sample Collection:

• Core biopsy
• Blood sample

28-day Cycle Treatment Regimen:

• Paclitaxel 90 mg/m2 IV D1, 8, and 15
• Avastin 10 mg/kg IV D1 and 15

ECOG Performance Status of 0 or 1

Life Expectancy: Not specified

Hematopoietic:

• Platelet count > 100,000/mm³
• Absolute neutrophil count > 1200/mm³
• PTT < 1.5 x upper limit of normal
• INR < 1.5 x upper limit of normal

Hepatic:

• Total bilirubin < 1.5 mg/dL
• SGOT (AST) < 2 x upper limit of normal

Renal: Not specified

Cardiovascular:

• Clinically significant cardiovascular or cerebrovascular disease including prior myocardial infarction (within 6 months prior to study entry), unstable angina, Grade II or greater peripheral vascular disease, New York Heart Association (NYHA) Grade II or greater congestive heart failure, hypertensive crises, hypertensive encephalopathy or uncontrolled hypertension (SBP>150, DBP>100).

Conditions

Breast Cancer

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Study Groups

Arm 1

Paclitaxel 90 mg/m2 IV D1, 8, and 15 + Avastin 10 mg/kg IV, day 1 and 15

Core Biopsy

Intervention Type: PROCEDURE

biopsy

Blood Collection

Intervention Type: PROCEDURE

Blood/serum sample

Paclitaxel

Intervention Type: DRUG

Paclitaxel 90 mg/m2 IV, day 1, 8 and 15

Avastin

Intervention Type: DRUG

Avastin 10 mg/kg IV, day 1 and 15

Interventions

Core Biopsy

biopsy

Intervention Type: PROCEDURE

Blood Collection

Blood/serum sample

Intervention Type: PROCEDURE

Paclitaxel

Paclitaxel 90 mg/m2 IV, day 1, 8 and 15

Intervention Type: DRUG

Avastin

Avastin 10 mg/kg IV, day 1 and 15

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed adenocarcinoma of the breast with measurable locally recurrent, locally advanced (that is not amenable to resection with curative intent), or metastatic disease.
• Patients must consent to have a biopsy performed to obtain fresh tissue or be able to identify a FFPE tissue block in which tissue samples can be obtained to complete the testing for this study.
• Planned chemotherapy regimen of paclitaxel and Avastin for the treatment of metastatic breast cancer.
• Females age > 18 years
• Written informed consent and HIPAA authorization for release of personal health information.

Exclusion Criteria

• Patients must not have had chemotherapy for locally recurrent or metastatic breast cancer.
• Hormonal therapy for locally recurrent or metastatic disease must have been discontinued at least 2 weeks prior to study entry.
• Patients must not have had adjuvant or neoadjuvant taxane therapy within 12 months prior to study entry.
• Breast cancer overexpressing HER-2 (gene amplification by FISH or 3+ overexpression by immunohistochemistry) are not eligible unless they have received prior therapy with Herceptin.
• Patients must not have had a major surgical procedure within 4 weeks prior to study entry. (Placement of vascular access device, and breast biopsy, will not be considered major surgery.)
• Patients must not have had a minor surgical procedure, placement of an access device, or fine needle aspiration within 7 days of starting protocol therapy.
• Patients must not have had radiation within 2 weeks prior to study entry.
• Previously radiated area(s) must not be the only site of disease for study entry.
• Patients must not have a history of bleeding diathesis or have used anticoagulant therapy within 10 days of study entry. (Low dose anticoagulant therapy to maintain patency of a vascular access device is allowed.)
• Patients with a history of deep vein thrombosis or pulmonary embolism are not eligible.
• Aspirin usage (> 325 mg/day) or other nonsteroidal anti-inflammatory medications known to inhibit platelet function daily are not allowed within 10 days prior to study entry.
• Patients currently using any of the following drugs known to inhibit platelet function are not eligible: dipyridamole (Persantine), ticlopidine (Ticlid), clopidogrel (Plavix) and cilostazol (Pletal).
• Patients must not have a history of TIA or CVA within 6 months prior to study entry.
• Patients must not have a history or radiologic evidence of CNS metastases including previously treated, resected or asymptomatic brain lesions or leptomeningeal involvement (head CT or MRI must be obtained within 6 weeks prior to study entry).
• Patients must not have a non-healing wound or fracture.
• Patients must not have a hypersensitivity to paclitaxel or drugs using the vehicle Cremophor, Chinese hamster ovary cell products or other recombinant human antibodies.
• Females must not be pregnant or breastfeeding. Females of childbearing potential must use an accepted and effective method of contraception (hormonal or barrier method of birth control; abstinence) while on treatment and for a 3 month period thereafter.
• Females of childbearing potential must have a negative pregnancy test within 7 days prior to being registered for protocol therapy. Subjects are considered not of child bearing potential if they are surgically sterile (they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal.
• History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to study entry
• Urine protein: creatinine (UPC) ratio > 1.0 at baseline or urine protein dipstick > 2+.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

United States Department of Defense

FED

Sponsor Role: collaborator

Indiana University School of Medicine

OTHER

Sponsor Role: collaborator

University of Colorado, Denver

OTHER

Sponsor Role: collaborator

Baylor University

OTHER

Sponsor Role: collaborator

McGill University

OTHER

Sponsor Role: collaborator

Hoosier Cancer Research Network

OTHER

Sponsor Role: lead

Responsible Party

Hoosier Oncology Group

Principal Investigators

George Sledge, M.D.

Role: PRINCIPAL_INVESTIGATOR

Hoosier Oncology Group, Inc.

Locations

Cancer Care Center of Southern Indiana

Bloomington, Indiana, United States

Indiana University Simon Cancer Center

Indianapolis, Indiana, United States

Horizon Oncology Center

Lafayette, Indiana, United States

Baylor College of Medicine - Methodist Breast Center

Houston, Texas, United States

Countries

United States

Related Links

http://www.hoosieroncologygroup.org

Hoosier Oncology Group Home Page

Other Identifiers

DoD Grant BC030400

Identifier Type: OTHER

Identifier Source: secondary_id

HOG COE-02

Identifier Type: -

Identifier Source: org_study_id