Ductal Carcinoma in Situ
Conditions
Keywords
DCIS, breast
Brief summary
The purpose of this study is to establish the utility of lapatinib in the treatment of DCIS, particularly ER-negative DCIS.
Detailed description
Ductal carcinoma in situ (DCIS) of the breast is a pre-malignant lesion of the breast, which is associated with a marked increase in the likelihood of developing invasive breast cancer. Since DCIS tends to be associated with microcalcifications, it is detected with an increased frequency in patients being screened with mammographic techniques. The treatment of DCIS is based on a number of parameters; local treatment depends on the size of the lesion, grade and margins. The only systemic treatment currently available is in the form of endocrine therapy; it depends on the expression of estrogen receptor (ER). Randomized trials have shown that the treatment of DCIS with breast conserving therapy and radiation is as effective as simple mastectomy. The efficacy of tamoxifen in reducing the incidence of further invasive or non-invasive breast cancer has been established. In addition to surgery (with or without radiation), patients with ER positive disease also receive anti-estrogen therapy. Current guidelines do not recommend any additional therapy for ER-negative DCIS. The rationale for the proposed study is based on the observations that HER2 is expressed at high levels in higher grades of DCIS, which typically lack ER. In addition, an inverse relationship between ER expression and the expression of EGFR has also been demonstrated. Lapatinib is active against both these receptors and may have therapeutic action in ER negative DCIS. We propose to treat the patients with drug in the interval between biopsy diagnosis and definitive surgery.
Interventions
DRUGlapatinib
1500 mg lapatinib for 14-21 days
Sponsors
GlaxoSmithKline
Indiana University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age greater than or equal to 18 years. 2. Patients with operable, biopsy-proven DCIS detected by screening mammography. 3. ER/PR negative DCIS. 4. DCIS that is positive for HER-2 &/or EGFR, which is defined as IHC 3+. 5. Women of childbearing potential willing to use an accepted and effective barrier method of contraception. 6. ECOG performance status ≤2 7. Cardiac ejection fraction within the institutional range of normal as measured by echocardiogram. 8. Ability to understand and the willingness to sign a written informed consent document. 9. Patients must have normal organ and marrow function as defined below: * leukocytes ≥3,000/microL * absolute neutrophil count ≥1,500/microL * platelets ≥100,000/microL * total bilirubin within normal institutional limits * AST (SGOT)/ALT(SGPT) within normal institutional limits * creatinine within normal institutional limits OR creatinine clearance greater than or equal to 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal (using Cockcroft-Gault formula)
Exclusion criteria
1. Invasive breast cancer 2. ER+ or PR+ DCIS 3. Pregnant or breast feeding women 4. Patients who have had prior treatment with EGFR targeting therapies. 5. Patients may not be receiving any other investigational agents or receiving concurrent anticancer therapy. In addition, all herbal (alternative) medicines are excluded one week before starting lapatinib and for the duration of lapatinib therapy. 6. Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements. 7. HIV-positive patients receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with lapatinib. 8. Have ANY hepatic or biliary disease or dysfunction. 9. Patients with GI tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis). 10. Concomitant requirement for medication classified as CYP3A4 inducers or inhibitors. 11. ANY history of cardiac disease.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Patients Where Gene Signature Was Obtained. | Up to 60 days | Number of patients where gene signature was obtained. This was used to identify gene signature that denotes effect of lapatinib therapy in breast cancer cell lines and to assess effect of lapatinib therapy in patients with ductal carinoma in situ of the breast using the gene signature developed as a surrogate marker. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Patients With Toxicity Associated With Short Therapy With Lapatinib. | Up to 60 days | Number of patients with toxicity associated with short therapy with lapatinib will be reported. |
Countries
United States
Participant flow
Recruitment details
Thirty patients were expected for this trial but it stopped at one patient due to difficulty with recruitment.
Participants by arm
| Arm | Count |
|---|---|
| 1500 mg Lapatinib for 14-21 Days Patients took 1500 mg Lapatinib for 14-21 days until surgical excision. | 1 |
| Total | 1 |
Baseline characteristics
| Characteristic | 1500 mg Lapatinib for 14-21 Days |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 0 Participants |
| Age, Categorical Between 18 and 65 years | 1 Participants |
| Age, Continuous | 63 years |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 1 Participants |
| Sex: Female, Male Female | 1 Participants |
| Sex: Female, Male Male | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 1 / 1 |
| serious Total, serious adverse events | 1 / 1 |
Outcome results
Primary
Number of Patients Where Gene Signature Was Obtained.
Number of patients where gene signature was obtained. This was used to identify gene signature that denotes effect of lapatinib therapy in breast cancer cell lines and to assess effect of lapatinib therapy in patients with ductal carinoma in situ of the breast using the gene signature developed as a surrogate marker.
Time frame: Up to 60 days
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1500 mg Lapatinib for 14-21 Days | Number of Patients Where Gene Signature Was Obtained. | 1 participants |
Secondary
Number of Patients With Toxicity Associated With Short Therapy With Lapatinib.
Number of patients with toxicity associated with short therapy with lapatinib will be reported.
Time frame: Up to 60 days
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| 1500 mg Lapatinib for 14-21 Days | Number of Patients With Toxicity Associated With Short Therapy With Lapatinib. | 1 participants |