Last updated: 11/03/2018 13:09:09
This product has been transferred to Novartis. GSK Clinical Study Register is no longer maintained for this study. The most up to date information is available on clinicaltrials.gov.
Lapatinib in Combination with VinorelbineVITAL
Clinicaltrials.gov ID
EudraCT ID
EU CT Number
Not applicable
Trial status
No longer a GSK study
No longer a GSK study
Trial overview
Official title: A Phase II, Randomised, Multi-Centre Study Evaluating Lapatinib in Combination with Vinorelbine or Capecitabine in Women with ErbB2 Overexpressing Metastatic Breast Cancer
Trial description: This is a randomized, parallel-arm, open-label, multi-centre, Phase II study to determine the efficacy and safety of lapatinib in combination with vinorelbine or capecitabine in women with ErbB2 overexpressing metastatic breast cancer (MBC) who have received no more than one chemotherapeutic regimen in the metastatic setting.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:
Progression Free Survival (PFS) in the Randomized Phase
Timeframe: From randomization until disease progression, death, or discontinuation from the study (average of 27 study weeks)
Secondary outcomes:
Number of participants with Grade 4 and Grade 5 adverse events (AE)
Timeframe: From randomization until disease progression, death, or discontinuation from the study (average of 55 study weeks)
Maximum concentration (Cmax) for vinorelbine
Timeframe: Days 1 and 8; 0 to 24 hours post-dose
Duration of response (DOR) in the Randomized Phase
Timeframe: From the time of the first documented confirmed complete or partial response until disease progression or death, if sooner (average of 27 study weeks)
Time to response in the Randomized Phase
Timeframe: From randomization until the time of the first documented confirmed CR or PR (average of 27 study weeks)
Number of participants with Overall Response (OR), as assessed by the investigator in the Randomized Phase
Timeframe: From randomization until disease progression, death, or discontinuation from the study (average of 27 study weeks)
Overall Survival (OS)
Timeframe: From the date of randomization until death (average of 55 study weeks)
Area under the concentration-time curve over the dosing interval (AUC-tau) for vinorelbine
Timeframe: Days 1 and 8; 0 to 24 hours post-dose
Number of participants with clinical benefit (CB) in the Randomized Phase
Timeframe: From randomization until disease progression, death, or discontinuation from the study (average of 27 study weeks)
Interventions:
Drug: Lapatinib
Drug: Capecitabine
Drug: Vinorelbine
Enrollment:
112
Observational study model:
Not applicable
Primary completion date:
2012-21-08
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Cancer, Neoplasms
Product
lapatinib, vinorelbine
Collaborators
Not applicable
Study date(s)
November 2009 to June 2016
Type
Interventional
Phase
2/3
Participation criteria
Sex
Female
Age
18+ years
Accepts healthy volunteers
none
- Inclusion Criteria :
- Signed informed consent prior to registration.
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion Criteria :
- Signed informed consent prior to registration.
- Considered by the investigator to have a life expectancy of ≥12 weeks.
- Subjects must be female and have histologically
- confirmed invasive breast cancer with Stage IV disease at primary diagnosis or at relapse after curative
- intent surgery.
- Documented overexpression of ErbB2
- Subjects should have progressive disease following prior therapy which may include anthracyclines, taxanes, and trastuzumab.
- Females aged ≥18 years
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 to 1.
- Subjects must have adequate organ and marrow function
- Subjects must have a cardiac ejection fraction of at least 50% and within the institutional range of normal.
- Radiotherapy prior to initiation of study medication is allowed to a limited area ( e . g . , palliative therapy ) , if it is not the sole site of disease.
- Subjects with stable central nervous system (CNS) metastases are permitted.
- Subject must be free of gastrointestinal diseases or any other conditions that impede swallowing, retaining, and absorption of oral medications.
- Bisphosphonate therapy for bone metastases is allowed; however, treatment must be initiated prior to the first dose of study medication. Prophylactic use of bisphosphonates in subjects without bone disease, except for the treatment of osteoporosis, is not permitted. Exclusion Criteria:
- Subjects taking prohibited medications are not eligible for the study.
- Therapy with lapatinib, vinorelbine, or capecitabine prior to randomization into this study.
- Prior therapy with more than one chemotherapeutic regimen for metastatic breast cancer.
- Concurrent anticancer or concomitant radiotherapy treatment.
- History of uncontrolled or symptomatic angina; history of arrhythmias requiring medications ; clinically significant myocardial infarction < 6 months from study entry; uncontrolled or symptomatic congestive heart failure; ejection fraction below the institutional normal limit; or any other cardiac condition, which in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient.
- Have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment).
- Use of an investigational drug within 30 days or 5 half
- lives, whichever is longer, preceding the first dose of investigational treatment, or, concurrent treatment with an investigational agent or participation in another clinical trial involving investigational agents.
- Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to any of the agents used in this study or their excipients that in the opinion of the investigator or GSK Medical Monitor contraindicates their participation.
- Known deficiency for the enzyme dihydropyrimidine dehydrogenase (DPD).
- Known history of uncontrolled inter
- current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, clinically significant cardiac arrhythmia, or psychiatric illness / social situations that would limit compliance with study requirements.
- Concurrent disease or condition that would make the subject inappropriate for study participation , or any serious medical disorder that would interfere with the subject’s safety.
- Pregnant or lactating females at any time during the study (due to the potential teratogenic or abortifacient effects of lapatinib and breastfeeding).
- Subjects with diseases affecting gastrointestinal function resulting in an inability to take oral medication , including ; malabsorption syndrome, disease significantly affecting gastrointestinal function , or resection of the stomach , small bowel , or colon. Subjects with inflammatory bowel disease or ulcerative colitis are also excluded.
- Peripheral neuropathy of Grade 2 or greater.
- Unresolved or unstable, serious toxicity from prior administration of another investigational drug and / or of prior cancer treatment.
- Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.
Trial location(s)
No location data available.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
No longer a GSK study
Actual primary completion date
2012-21-08
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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Access to clinical trial data by researchers
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