Presurgical Therapy With Lapatinib to Explore Molecular Determinants of Response to EGFR/erbB2 Targeted Therapy

Breast Cancer Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00343759
• Other study ID #: 803893
• Secondary ID: UPCC 12104
• Status: Withdrawn
• Phase: Phase 2
• First received: June 21, 2006
• Last updated: December 9, 2015
• Start date: June 2006
• Est. completion date: December 2009

Study information

• Verified date: December 2015
• Source: University of Pennsylvania
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to see what kinds of breast tumors will respond to lapatinib. Lapatinib is an experimental medicine which may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically-confirmed by either core or fine needle biopsy primary invasive carcinoma of the breast;

• AJCC T2-T3 disease (>2.0 cm without chest wall or skin invasion) by at least one imaging modality (either mammogram, ultrasound, or MRI) - entry criteria is based on radiologic staging and not final pathologic staging;

• ECOG performance status 0-1 (Karnofsky = 70%

• Any lymph node status, hormone receptor status, and level of erbB2 expression

• No prior chemotherapy, hormonal therapy or radiation therapy to the affected breast for current or previous malignancy;

• Cardiac ejection fraction >50% or within the institutional range of normal;

• Patients must have normal organ and marrow function defined as: Leukocyte count >3000/uL; Absolute neutrophil count (ANC) = 1,500/mm3, platelets > 100,000/mm3, and hemoglobin = 8 gm/dl; Serum creatinine = 1.5 times ULN, or 24-hour creatinine clearance = 75 cc/min; Serum bilirubin = 1.5 times ULN; SGOT = 2.5 times ULN; alkaline phosphatase = 2.5 ULN times ULN.

• The effects of lapatinib on the developing human fetus at the recommended therapeutic dose are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.

• Ability to understand and the willingness to sign written informed consent document.

Exclusion Criteria:

• AJCC T1, T4, or stage 4 disease;

• Patients may not have undergone incisional or excisional biopsy of their tumor;

• Patients may not be receiving any other investigational agents;

• Absolute contraindication to MRI imaging (cardiac pacemaker or any non-removable metallic foreign object in the body);

• On chronic therapy with any known inducer or inhibitor of CYP3A4

• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

• Pregnant or lactating women are excluded from this study because lapatinib is a tyrosine kinase inhibitor with the potential for teratogenic or abortifacient effects.

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer

Intervention

Drug:
• Lapatinib
Patients will take 14 days of Lapatinib prior to definitive surgery.

Locations

Country	Name	City	State
United States	Abramson Cancer Center of University of Pennsylvania	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in downstream effector levels in biologic responders to lapatinib as determined by degree of change in proliferation and apoptosis compared to biologic non-responders.		Study completion	No
Secondary	To describe the biologic response rate, defined by induction of apoptosis, to Lapatinib in a pre-surgical, treatment-naïve breast cancer population.		Study completion	No