PhaseII study of gefitinib combined with cisplatin and pemetrexed in patients with advanced non-squamous, non-small cell lung cancer acquired resistance to first line gefitinib monotherapy.
- Conditions
- on-small cell lung cancer
- Registration Number
- JPRN-UMIN000005690
- Lead Sponsor
- Division of Thoracic Oncology, Shizuoka Cancer Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Not provided
1) Impossible cases with protcol defined oral administration. 2) Patients with symptomatic brain metastasis. 3) With active lung disease such as interstitial pneumonia, pneumoconiosis, active radiation pneumonitis,or drug-induced pneumonitis. 4) Thoracic radiation, within 4 weeks, irradiation to other organs within 2 weeks. 5) Uncontrollable pleural or pericardial effusion. 6) Operation within 4 weeks. 7) Active infection. 8) Active concomitant malignancy. 9) Severe drug allergy. 10) Pregnant or breast-feeding woman. 11) Inappropriate patients for this study judged by the physicians.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 6 months progression free survival rate
- Secondary Outcome Measures
Name Time Method Overall survival Response rate Progression free survival Adverse events