Phase 2
N=87
Lapatinib in Combination With Trastuzumab in Patients With HER2-Positive, Metastatic Breast Cancer
Breast Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00470704 ↗Enrolled (actual)
87
Serious AEs
10.3%
Results posted
Mar 2022
Primary outcome: Primary: Objective Response Rate — 50.0; 22.2 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Lapatinib (Drug); Herceptin (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Nancy Lin, MD
- Primary completion
- Nov 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Objective Response Rate |
50.0; 22.2 | — |
| SECONDARY Top 3 Most Common Treatment RelatedToxicities |
27; 28; 21; 24; 20; 15 | — |
| SECONDARY Sites of First Progression |
3; 3; 31; 39; 3; 0 | — |
| SECONDARY Clinical Benefit Rate |
57.5; 40.0 | — |
| SECONDARY 3-Year Overall Survival |
.62; .39 | — |
| SECONDARY Median Time to Progression |
7.4; 5.3 | — |
Summary
In this research study we are studying the effects of the combination of lapatinib plus Herceptin in subjects with breast cancer that has spread outside of the breast. We are also studying whether positron emission tomography (PET/CT) scans can predict which participants will benefit from the study treatment. Finally, we are studying genes and proteins in the tumor tissue that may lead to sensitivity or resistance to Herceptin, and to the combination of Herceptin plus lapatinib. Lapatinib is a compound that may stop cancer cells from growing. Other research studies suggest that lapatinib in combination with Herceptin may help to shrink or stabilize breast cancer.
Eligibility Criteria
Inclusion Criteria
- Histologically or cytologically confirmed invasive breast cancer, with stage IV disease
- HER2-positive breast cancer, defined as 3+ staining by IHC or gene amplification by FISH
- Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension
- Willingness to undergo a research biopsy of recurrent or metastatic disease
- Prior chemotherapy treatment must be discontinued for at least 2 weeks prior to study entry.
- Completed radiation therapy at least 7 days prior to beginning protocol treatment
- Cohort 1: No prior chemotherapy for advanced breast cancer; no prior trastuzumab in the advanced breast cancer setting; nor prior treatment with lapatinib or other HER2-directed therapy other than trastuzumab
- Cohort 2: Up to two prior chemotherapy regimens for the treatment of advanced breast cancer; no prior treatment with lapatinib or other HER2-directed therapy except for trastuzumab
- 18 years of age or older
- Life expectancy of greater than 12 weeks
- ECOG Performance Status 0-2
- Normal organ and marrow function as outlined in protocol
- Cardiac ejection fraction, as assessed by either MUGA scan or echocardiogram greater than or equal to 50%
- Able to take oral medications
Exclusion Criteria
- Patients may not be receiving any other investigational agents or concurrent chemotherapy or hormonal therapy for treatment of metastatic disease
- Active brain metastases
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to lapatinib or other agents used in this study
- Clinically significant malabsorption syndrome
- Uncontrolled intercurrent illness
- Pregnant or breastfeeding women
- Concurrent use of the medications listed in the protocol because of possible interaction with lapatinib
Data sourced from ClinicalTrials.gov (NCT00470704). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.