Breast Cancer Clinical Trial

Lapatinib Resistance in Patients With Breast Cancer

Summary

RATIONALE: Studying samples of tumor tissue and blood from patients with cancer in the laboratory may help doctors learn more about cancer and the development of drug resistance in patients.

PURPOSE: This research study is looking at lapatinib resistance in patients with breast cancer.

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Full Description

OBJECTIVES:

To identify secondary ErbB2 mutations in tumor tissue samples from patients with ErbB2-positive breast cancer treated with lapatinib ditosylate.
To investigate ErbB2 copy number changes and expression levels.
To determine abnormalities of other pathways (e.g., c-MET and PI3K) as potential mechanisms of resistance.

OUTLINE: Previously collected tumor tissue samples* are obtained for genetic analysis studies. Samples are analyzed for secondary ErbB2 mutations by nested PCR; ErbB2 copy number changes by quantitative PCR and standard histological FISH; and ErbB2 expression levels by quantitative RT-PCR and IHC. Patients also undergo blood sample collection for extraction of DNA (as normal control DNA) and isolation of EpCAM-positive circulating tumor cells using immunomagnetic cell separation technology. Additional research studies may include mutational and amplification analysis of the c-MET and PI3K pathways.

NOTE: *Patients may undergo biopsy if a post-treatment tumor tissue sample is unavailable.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Pathologically confirmed invasive breast cancer

ErbB2-positive disease

Has received or is currently receiving lapatinib ditosylate

Documented clinical benefit while receiving lapatinib ditosylate (e.g., stable disease of ≥ 12 weeks duration OR a radiographic response)
Must have tumor tissue samples available for research studies
Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Menopausal status not specified
Not pregnant*
Coagulation profile normal*
Platelet count > 100,000/mm³* NOTE: *For patients requiring a post-treatment biopsy

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
Concurrent chemotherapy or trastuzumab (Herceptin®) allowed
No concurrent anticoagulants, including warfarin or low-molecular weight heparin*
No concurrent antiplatelet therapy, including aspirin, clopidogrel, or other antiplatelet agents* NOTE: *For patients requiring a post-treatment biopsy

Study is for people with:

Breast Cancer

Study ID:

NCT00898573

Recruitment Status:

Withdrawn

Sponsor:

Case Comprehensive Cancer Center

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There are 9 Locations for this study

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Geauga Regional Hospital
Cleveland Ohio, 44024, United States
Lake/University Ireland Cancer Center
Cleveland Ohio, 44060, United States
Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center
Cleveland Ohio, 44106, United States
University Suburban Health Center
Cleveland Ohio, 44121, United States
UHHS Chagrin Highlands Medical Center
Cleveland Ohio, 44122, United States
Southwest General Health Center
Cleveland Ohio, 44130, United States
UHHS Westlake Medical Center
Cleveland Ohio, 44145, United States
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
Cleveland Ohio, 44195, United States
Mercy Cancer Center at Mercy Medical Center
Cleveland Ohio, 44708, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT00898573

Recruitment Status:

Withdrawn

Sponsor:


Case Comprehensive Cancer Center

How clear is this clinincal trial information?

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