Extension Study of Lapatinib Plus Herceptin With or Without Endocrine Therapy

Status: Recruiting
Phase: Phase 2
Diagnosis: Breast: Early Stage Disease
NCT ID: NCT00999804 (View complete trial on ClinicalTrials.gov)
DFCI Protocol ID: 12-226

 

Breast cancer is the most common malignancy in the U.S. Targeted therapies such as tamoxifen have been revolutionary in reducing tumor recurrences and mortality in early breast cancer. Using this successful paradigm, there has been a continued search for other targeted biologic therapies directed at receptors with known potential for promoting tumor growth. The estrogen receptor (ER) and/or the HER signaling pathways are the dominant drivers of cell proliferation and survival in the majority of human breast cancers. Molecular targets of these pathways provide the most effective therapies in appropriately selected patients. However, de novo and acquired resistance remain major obstacles to successful treatment, and understanding the molecular pathways responsible for this resistance would enable the discovery of new strategies to overcome it. The superiority of multi-drug HER2-targeted therapy over single agent therapy has been demonstrated in the preclinical setting using mouse xenografts. Trastuzumab, pertuzumab, lapatinib, and gefitinib, represent a group of therapeutic agents that target the HER family by different molecular mechanisms. Used as single agents in the MCF7/HER2-18 xenograft model, these drugs restored or enhanced sensitivity to tamoxifen. However, tumor growth inhibition lasted only 2-3 months before resistance to treatments occurred. However, when gefitinib, a HER1 inhibitor, was added to the two-antibody (T+P) regimen to block signals from HER1 dimers, a complete disappearance of nearly all xenograft tumors was observed; moreover, there was evidence of complete tumor eradication in 50% of the mice. The combination of lapatinib + trastuzumab was also highly effective in eradication of tumor burden, with no evidence of re-growth after 200 days. These xenograft models demonstrate that multi-drug HER2-targeted therapy more effectively induces apoptosis and inhibits proliferation, thereby resulting in tumor regression. Furthermore, HER2 combination therapy appears to more effectively reduce levels of phosphorylated pAKT and MAPK, thus resulting in sustained tumor inhibition.

 

Conducting Institutions:
Brigham and Women's Hospital, Dana Farber Cancer Institute at Faulkner Hospital, Dana-Farber Cancer Institute

Overall PI:
Ian Krop, MD, Dana-Farber Cancer Institute

Site-responsible Investigators:
Erica Mayer, MD, Dana-Farber Cancer Institute

Contacts:
Dana-Farber Cancer Institute: Breast Cancer Nursing Team, 617-632-3478

Eligibility Criteria

Inclusion Criteria: 1. All patients must be female and at least 18 years of age. 2. Signed informed consent. 3. Locally advanced breast cancers are eligible. Locally advanced cancers must be of clinical and/or radiologic size >3 cm, or >2 cm with clinical evidence of axillary nodal involvement*. (If tumors are less than 3 cm, we will use the radiologically measured tumor size to determine if the tumor meets the minimal size requirements.) 4. Patients must have histologically confirmed invasive mammary carcinoma that is HER2 overexpressing, defined as 3+ by immunohistochemistry, or a FISH/CEP ratio greater than 2. 5. Negative serum pregnancy test (HCG) within 7 days of starting study drug, if of child-bearing potential. 6. Kidney and liver function tests - all within 1.5 times the institutional upper limit of normal. 7. Performance status (WHO/ECOG scale) 0-1 and life expectancy >6 months. 8. No evidence of brain or leptomeningeal disease, or any other Stage IV disease. 9. No previous or current malignancies at other sites within the last 5 years, with exception of adequately treated cone-biopsied in situ carcinoma of the cervix uteri and basal or squamous cell carcinoma of the skin. Exclusion Criteria: 1. Patients with bilateral breast cancer. 2. Pregnancy or unwillingness to use a reliable contraceptive method in women of child-bearing potential. 3. Severe underlying chronic illness or disease. 4. Cardiomyopathy or baseline LVEF less than 50%. 5. Other investigational drugs while on study. 6. Severe or uncontrolled hypertension, history of congestive heart failure or severe coronary arterial disease. 7. Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel. Subjects with ulcerative colitis are also excluded 8. Taking any lapatinib prohibited medication(s) 9. Inability or unwillingness to comply with, or follow study procedures. 10. Patients who have received any form of treatment for breast cancer within the past five years, including surgical resection, chemotherapy, endocrine therapy, or biologic therapy. 11. Patients with a prior history of ipsilateral invasive breast cancer or carcinoma in situ who present with a new primary. 12. Patients with known active, infectious Hepatitis B, Hepatitis C, or HIV.
  • Email
  • Print
  • Share
  • Text
Highlight Glossary Terms