- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00111787
Study Of Lapatinib In Combination With Paclitaxel In The Treatment Of Newly Diagnosed Inflammatory Breast Cancer
May 27, 2017 updated by: GlaxoSmithKline
A Phase II Study to Evaluate the Efficacy, Safety, and Pharmacodynamics of Lapatinib in Combination With Paclitaxel as Neoadjuvant Therapy in Patients With Newly Diagnosed Inflammatory Breast Cancer
This Study was designed to determine how effective and safe a new investigational drug, lapatinib, is in combination with paclitaxel in treating patients with newly diagnosed inflammatory breast cancer.
Tumor tissue collected pre-treatment, following 14 days of treatment and at the time of surgical resection will be examined for pathologic response and biologic activity by IHC (immunohistochemistry) within the tumor.
Treatment will consist of 14 days of lapatinib monotherapy followed by 12 weeks of combination therapy with lapatinib and paclitaxel.
Blood samples for hematology and chemistry panels, MUGA/ECHO exams and physical exams will be performed throughout the study to monitor safety.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
49
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New South Wales
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Campbelltown, New South Wales, Australia, 2560
- GSK Investigational Site
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Liverpool, New South Wales, Australia, 2170
- GSK Investigational Site
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Randwick, New South Wales, Australia, 2031
- GSK Investigational Site
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Queensland
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South Brisbane, Queensland, Australia, 4101
- GSK Investigational Site
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South Australia
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Bedford Park, South Australia, Australia, 5042
- GSK Investigational Site
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Victoria
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Box Hill, Victoria, Australia, 3128
- GSK Investigational Site
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Ringwood East, Victoria, Australia, 3128
- GSK Investigational Site
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Ontario
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Toronto, Ontario, Canada, M4N 3M5
- GSK Investigational Site
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Bayonne, France, 64100
- GSK Investigational Site
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Lille Cedex, France, 59020
- GSK Investigational Site
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Paris cedex 13, France, 75651
- GSK Investigational Site
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Ramat Gan, Israel, 52621
- GSK Investigational Site
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Auckland, New Zealand
- GSK Investigational Site
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Barcelona, Spain, 08035
- GSK Investigational Site
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Girona, Spain, 17007
- GSK Investigational Site
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Valencia, Spain, 46010
- GSK Investigational Site
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Sfax, Tunisia, 3000
- GSK Investigational Site
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Sfax, Tunisia, 3029
- GSK Investigational Site
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Tunis, Tunisia, 1007
- GSK Investigational Site
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Tunis, Tunisia, 1004
- GSK Investigational Site
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London, United Kingdom, SW3 6JJ
- GSK Investigational Site
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Florida
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Miami, Florida, United States, 33136
- GSK Investigational Site
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Illinois
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Chicago, Illinois, United States, 60637
- GSK Investigational Site
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Zion, Illinois, United States, 60099
- GSK Investigational Site
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Texas
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Houston, Texas, United States, 77030
- GSK Investigational Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion criteria:
- Tumor accessible for multiple biopsies
- ECOG (Eastern Cooperative Oncology Group) performance status 0-2
- Adequate bone marrow
- Renal and hepatic function
- LVEF (left ventricular ejection fraction) greater than 0% based on ECHO (echocardiogram) or MUGA (multigated acquisition).
Exclusion criteria:
- Females who are pregnant or nursing.
- Any unstable, pre-existing major medical condition.
- Received an investigational drug within the past 4 weeks.
- Had major surgery in the past 2 weeks.
- Currently receiving amiodarone or has received amiodarone in the past 6 months.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Overall study
A Single arm study with 2 cohorts of participants.
Cohort A consists of participants with tumors overexpressing HER2 and/or EGFR.
Cohort B consists of participants with tumors expressing EGFR without overexpressing HER2.
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Daily-monotherapy [1500 milligrams (mg)] for 14 days, then daily combination therapy (with weekly paclitaxel) for 12 weeks
Weekly (80mg/m^2) combination therapy (with daily Lapatinib) for 12 weeks
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Percentage of participants with pathologic complete response rate (pCR)
Time Frame: Week 12
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pCR was defined as the percentage of participants who achieved an assessment of complete response (CR) following pathologic review of resected tissue.
CR was the disappearance of all target lesions.
Participants in each cohort with unknown or missing response (i.e., those that did not undergo surgery) were included in the denominator when calculating the percentage.
From an efficacy standpoint, the HER2+ population response was considered to be of special interest.
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Week 12
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Percentage of participants with pCR that underwent surgical resection
Time Frame: Week 12
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pCR for participants that underwent surgical (surg) resection was defined as the percentage of participants within each cohort who achieved an assessment of CR following pathologic review of resected tissue.
CR was the disappearance of all target lesions.
Participants in each cohort that did not undergo surgical resection were excluded from the denominator when calculating the percentage.
From an efficacy standpoint, the HER2+ population response was considered to be of special interest.
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Week 12
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Percentage of participants with objective response rate (ORR) at the end of study (Response evaluation criteria in solid tumor [RECIST])
Time Frame: Week 14
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ORR at the end of the study was defined as the number of participants within each cohort who had a confirmed CR or partial response (PR) at the end of the study divided by the total number of participants enrolled in each cohort.
CR was the disappearance of all target lesions.
PR was at least a 30 percent decrease in the sum of the longest diameter of target lesions, taking as a reference, the Baseline sum longest diameter.
Each participant's response was based on the investigator assessment of best response using RECIST criteria.
Participants in each cohort with unknown or missing response was treated as non-responders; i.e. they were included in the denominator when calculating the percentage.
From an efficacy standpoint, the HER2+ population was considered to be of special interest.
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Week 14
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Percentage of participants with ORR at the end of study (Clinically Evaluable Skin Disease Criteria)
Time Frame: Week 14
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ORR at the end of the study was defined as the number of participants within each cohort who had a confirmed CR or PR at the end of the study divided by the total number of participants enrolled in each cohort.
CR was the disappearance of all target lesions.
PR was at least a 30 percent decrease in the sum of the longest diameter of target lesions, taking as a reference, the Baseline sum longest diameter.
Each participant's response was based on the investigator assessment of best response using Clinically Evaluable Skin Disease Criteria.
Participants in each cohort with unknown or missing response was treated as non-responders; i.e. they were included in the denominator when calculating the percentage.
From an efficacy standpoint, HER2+ population was considered to be of special interest.
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Week 14
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Percentage of participants with ORR at the end of study ('Best' of RECIST and Clinically Evaluable Skin Disease Criteria)
Time Frame: Week 14
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ORR at the end of the study was defined as the number of participants within each cohort who had a confirmed CR or PR at the end of the study divided by the total number of participants enrolled in each cohort.
CR was the disappearance of all target lesions.
PR was at least a 30 percent decrease in the sum of the longest diameter of target lesions, taking as a reference, the Baseline sum longest diameter.
The best response of the participant was defined by the 'Best' combined response (RECIST and Clinically Evaluable Skin Disease Criteria) provided there is no evidence of disease progression.
Participants in each cohort with unknown or missing response was treated as non-responders; i.e. they were included in the denominator when calculating the percentage.
From an efficacy standpoint, the HER2+ population was considered to be special interest.
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Week 14
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Percentage of participants with investigator-Assessed Best Response at the end of monotherapy phase (Day 14) (Clinically Evaluable Skin Disease Criteria)
Time Frame: Day 14
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ORR at the end of the monotherapy phase was defined as the percentage of participants within each cohort who had a confirmed CR or PR at the end of lapatinib monotherapy (Day 14) divided by the total number of participants enrolled in each cohort.
CR was the disappearance of all target lesions.
PR was at least a 30 percent decrease in the sum of the longest diameter of target lesions, taking as a reference, the Baseline sum longest diameter.
Each participant's response was based on the investigator assessment of best response using clinically evaluable skin disease criteria.
Participants in each cohort with unknown or missing response was treated as non-responders; i.e. they were included in the denominator when calculating the percentage.
From an efficacy standpoint, the HER2+ population was considered to be special interest.
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Day 14
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Number of participants with adverse events (AEs) and serious adverse events (SAEs)
Time Frame: Up to Week 14, surgical resection and post treatment
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An AE was defined as any untoward medical occurrence in a participant or clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.
An SAE was defined as any untoward medical occurrence that, at any dose that resulted in death, was life-threatening, required hospitalization or prolongation of existing hospitalization, resulted in disability/incapacity or was a congenital anomaly/birth defect, resulted in deterioration in left ventricular cardiac function and caused Grade 3 or 4 interstitial pneumonitis.
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Up to Week 14, surgical resection and post treatment
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Number of participants with shift from Baseline in hematological toxicity grade
Time Frame: Day 14 and up to Week 23, surg resection and post treatment
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Hematology was summarized for hemoglobin (Hb), platelets, white blood cell count (WBC), neutrophils (Neu), lymphocytes by scheduled assessment and also according to the maximum common terminology criteria (CTC) toxicity grade.
Baseline was the most recent lab value prior to and within two weeks of the first dose of lapatinib.
Change from Baseline was calculated as the value at each visit minus Baseline value.
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Day 14 and up to Week 23, surg resection and post treatment
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Number of participants with shift from Baseline in clinical chemistry toxicity grade
Time Frame: Day 14, Week 4, 8, 12, 16, 20, Surg resection and post treatment
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Clinical chemistry was summarized for sodium, potassium (K), bicarbonate (bicarb), albumin (alb), calcium, gamma glutamyl transferase (GGT), creatinine (creat), total bilirubin (TB), alkaline phosphatase (ALP), aspartate amino transferase (AST) and alanine amino transferase (ALT) by scheduled assessment and also according to the maximum CTC toxicity grade.
Baseline was the most recent lab value prior to and within two weeks of the first dose of lapatinib.
Change from Baseline was calculated as the value at each visit minus Baseline value.
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Day 14, Week 4, 8, 12, 16, 20, Surg resection and post treatment
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Change from Baseline in vital signs- Systolic blood pressure (SBP) and Diastolic blood pressure (DBP)
Time Frame: Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Vitals signs (SBP and DBP) were assessed from screening until the post treatment phase.
Baseline was the most recent blood pressure (BP) mean prior to the first dose of lapatinib.
Change from Baseline was calculated as the mean at each visit minus the mean at Baseline.
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Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Change from Baseline in vital signs- Heart Rate (HR)
Time Frame: Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Vitals signs (HR) were assessed from screening until the post treatment phase.
Baseline was the most recent BP mean prior to the first dose of lapatinib.
Change from Baseline was calculated as the mean at each visit minus the mean at Baseline.
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Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Change from Baseline in vital signs- Body temperature
Time Frame: Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Vitals signs (body temperature) were assessed from screening until the post treatment phase.
Baseline was the most recent BP mean prior to the first dose of lapatinib.
Change from Baseline was calculated as the mean at each visit minus the mean at Baseline.
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Day 14, Week 1 and up to Week 24, surg resection and post treatment
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Number of participants with abnormal electrocardiogram (ECG) findings
Time Frame: Screening and unscheduled
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ECG was performed at screening and at unscheduled visits.
Participants with abnormal clinically significant and abnormal not clinically significant ECG findings was reported.
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Screening and unscheduled
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Number of participants with change from Baseline in echocardiogram (ECHO) or Multi-gated angiogram (MUGA) results at any post Baseline visit
Time Frame: Screening, Week 8, 16, 24, post treatment
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For ECHO and MUGA scans, the left ventricular ejection fraction (percent) was summarized for each scheduled assessment.
Absolute change from Baseline was summarized according to the following categories: any increase, 0 to less than 20 percent decrease, >=20 percent decrease or >=20 percent decrease and below the lower limit of normal (LLN).
Baseline was the most recent ECOG evaluation prior to the first dose of lapatinib.
Change from Baseline was calculated as the value at the post treatment minus Baseline value.
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Screening, Week 8, 16, 24, post treatment
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 11, 2005
Primary Completion (Actual)
November 1, 2006
Study Completion (Actual)
November 1, 2006
Study Registration Dates
First Submitted
May 25, 2005
First Submitted That Met QC Criteria
May 25, 2005
First Posted (Estimate)
May 26, 2005
Study Record Updates
Last Update Posted (Actual)
May 31, 2017
Last Update Submitted That Met QC Criteria
May 27, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Skin Diseases
- Neoplasms
- Neoplasms by Site
- Breast Diseases
- Breast Neoplasms
- Inflammatory Breast Neoplasms
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Antineoplastic Agents
- Tubulin Modulators
- Antimitotic Agents
- Mitosis Modulators
- Antineoplastic Agents, Phytogenic
- Protein Kinase Inhibitors
- Paclitaxel
- Lapatinib
Other Study ID Numbers
- EGF102580
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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