Paclitaxel and Irinotecan in Advanced Gastric Cancer
- Sponsor
- Seoul National University Hospital
- Study ID
- NCT01136031
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Advanced Gastric Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Paclitaxel and irinotecan — DRUGIn phase I part, Level Paclitaxel (mg/m²) Irinotecan (mg/m²) 1. 100 100 2. 100 120 3. 135 120 4. 135 160 every 3 week
Study Details
* Usually the combination of fluoropyrimidine with platinum is used as a first line chemotherapy (for example, 5-FU+cisplatin, capecitabine+cisplatin, S-1+ cisplatin, 5-FU+oxaliplatin) in advanced gastric cancer. * After failure with this combination, taxane-based regimen or irinotecan-based regimen is usually used. But, as a second-line regimen, the combination of topoisomerase inhibitor with taxane has not been fully evaluated until now. * So we designed this phase I/II study to evaluate the efficacy and toxicity of second-line chemotherapy with paclitaxel and irinotecan in fluoropyrimidine and platinum-pretreated advanced gastric cancer.
Key Dates
- Start date
- Jan 31, 2008
- Status verified
- May 2010
- Primary completion
- Jun 30, 2011
- Completion
- Aug 31, 2011
Study Design
- Enrollment
- 42 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Paclitaxel and irinotecan
Primary Outcome Measure
Dose-limiting toxicity (phase I part) [ Time Frame: during first cycle (first 3 week) ]
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