A Randomized, Open-label Phase III Study of First-line Treatment With Erlotinib Intercalated With Gemcitabine/ Cisplatin or Carboplatin Therapy Versus Erlotinib in Stage IIIB/IV NSCLC Patients With EGFR Mutation
Overview
- Phase
- Phase 3
- Intervention
- gemcitabine; cisplatin or carboplatin; erlotinib
- Conditions
- Non-Small Cell Lung Cancer
- Sponsor
- Xinjiang Medical University
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Progression-free survival
- Last Updated
- 12 years ago
Overview
Brief Summary
This 2 arm study will compare the efficacy and safety of treatment with erlotinib intercalated with platinum-based therapy or erlotinib along, as first line treatment in Stage IIIB/IV Non-Small Cell Lung Cancer Patients With Epidermal Growth Factor Receptor (EGFR) Mutation. Patients will be randomized to receive gemcitabine (1000mg/m2 iv) on days 1 , and cisplatin (75mg/m2) or carboplatin (5xAUC)on day 1, followed by erlotinib 150mg/day from day 15 to day 28 of each 4 week cycle for a total of 6 cycles,then followed by erlotinib monotherapy, or erlotinib 150mg/day .The anticipated time on study treatment is until disease progression, and the target sample size is 60 individuals.
Investigators
li shan
chief physician
Xinjiang Medical University
Eligibility Criteria
Inclusion Criteria
- •adult patients, \>=18 years of age;advanced (stage IIIB/IV)non-small cell lung cancer;measurable disease;ECOG Performance Status 0-2.
Exclusion Criteria
- •prior exposure to agents directed at the HER axis;prior chemotherapy or systemic anti-tumor therapy after advanced disease;unstable systemic disease; any other malignancy within last 5 years, except cured basal cell cancer of skin or cured cancer in situ of cervix.
Arms & Interventions
erlotinib combine with chemotherapy
Drug: gemcitabine 1000mg/m2 iv on days 1 of each 4 week cycle for 6 cycles Drug: Platinum chemotherapy (cisplatin or carboplatin) cisplatin --75mg/m2 oon day 1 of each 4 week cycle for 6 cycles or carboplatin--5xAUC on day 1 of each 4 week cycle for 6 cycles Drug: Erlotinib\[Tarceva\] po on days 15-28 of each 4 week cycle until disease progression
Intervention: gemcitabine; cisplatin or carboplatin; erlotinib
erlotinib along
Drug: erlotinib \[Tarceva\] 150mg/day po until disease progression
Intervention: erlotinib
Outcomes
Primary Outcomes
Progression-free survival
Time Frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months
Secondary Outcomes
- Overall Survival(From date of randomization until the date of death from any cause, assessed up to 24 mont)