Breast Cancer Clinical Trial

Phase I/II Study of MK-0752 Followed by Docetaxel in Advanced or Metastatic Breast Cancer

Summary

New and better therapies for locally advanced and metastatic breast cancer are needed because, even if standard treatment is successful in shrinking the cancer, there is still a high chance that the cancer will recur. Recent research suggests that breast tumors have a small number of cells in them that are "breast cancer stem cells", which are very resistant to standard treatment. It is thought that the reason that many patients cannot be cured of their breast cancers is that the stem cells are unable to be killed and remain in the body after standard treatment. Laboratory research has shown that a new drug, MK-0752, can target stem cells and prevent tumor recurrences when the drug is combined with docetaxel, a chemotherapy drug commonly used to treat breast cancer.

We know that MK-0752 is safe when given by itself to people. We do not know if treatment with MK-0752 and docetaxel combined is safe or if it will kill "breast cancer stem cells" in people with breast cancer. This clinical trial is being done to determine the safety of several doses of MK-0752 in combination with docetaxel. Preliminary data about the effectiveness of MK-0752 in combination with docetaxel will be collected. Also, tumor biopsy samples will be taken from some patients who have tumors that can be easily biopsied. The samples will be used to perform research tests to help determine if the "breast cancer stem cells" are being killed by the drug combination.

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Full Description

Purpose-Accumulating evidence supports the existence of breast cancer stem cells (BCSCs), which are characterized by their capacity to self-renew and divide indefinitely, and resistance to conventional therapies. The Notch pathway is important for stem cell renewal, and is a potential target for BCSC-directed therapy. Experimental Design-Using human breast tumorgraft studies, we evaluated the impact of gamma secretase inhibitors (GSI) on the BCSC population and the efficacy of combining GSI with docetaxel treatment. The mouse experimental therapy paralleled a concurrent clinical trial in advanced breast cancer patients, designed to determine the maximally tolerated dose of the GSI, MK-0752, administered sequentially with docetaxel, and to evaluate BCSC markers in serial tumor biopsies.

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Eligibility Criteria

Inclusion Criteria:

Men or women with metastatic (Stage IV) breast cancer, or with locally advanced breast cancer (Stages IIIA > 10 cm, or Stages IIIB and IIIC) that did not respond to first-line anthracycline-based chemotherapy, for whom docetaxel is a recommended therapy
Presence of measurable or evaluable disease
Adequate organ function
Ability to swallow intact study drug capsules
Zubrod Performance Status of 0-1 with at least a 3 month life expectancy
Appropriate time must have elapsed since prior anti-neoplastic therapy with resolution of acute toxicity

Exclusion Criteria:

Concurrent treatment with hormonal therapy intended to treat cancer
Radiotherapy within 7 days prior to first dose
Symptomatic central nervous system, and/or epidural metastases or symptomatic carcinomatous meningitis or with radiation treatment completed within the past 8 weeks
Serious comorbid illness which will limit the ability of the patient to safely receive anticancer treatment
Patients who are pregnant or nursing
Confounding factors present to provide misinterpretation of data (i.e., concurrent malignancy)

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00645333

Recruitment Status:

Completed

Sponsor:

University of Michigan Rogel Cancer Center

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There are 3 Locations for this study

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Dana Farber Cancer Institute
Boston Massachusetts, 02115, United States
University of Michigan Cancer Center
Ann Arbor Michigan, 48109, United States
Baylor College of Medicine
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00645333

Recruitment Status:

Completed

Sponsor:


University of Michigan Rogel Cancer Center

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