Back to Search
Start Over
Multicenter Phase II Study of a New Effective S-1 and Irinotecan Combination Schedule in Patients with Unresectable Metastatic or Recurrent Colorectal Cancer.
- Source :
-
Clinical Medicine Insights: Oncology . 2013, Issue 7, p21-30. 10p. 4 Charts, 3 Graphs. - Publication Year :
- 2013
-
Abstract
- Introduction: This multicenter phase II study determined the efficacy and safety of new daily oral S-1 and weekly irinotecan (CPT-11) combination schedule in patients with previously untreated advanced or recurrent colorectal cancer. Patients and methods: Patients received first-line chemotherapy comprising S-1 80 mg/m2/day given on days 3 to 7, 10 to 14, and 17 to 21 and 60 mg/m2 CPT-11 administered intravenously on days 1, 8, and 15 of a 28-day cycle. Results: A total of 45 eligible patients were enrolled in this study. The overall response rate was 48.9%. Median progression-free survival and median overall survival was 8.1 months and 20.9 months, respectively. The rates of grade 3 or 4 toxicity were as follows: neutropenia, 8.9%; anemia, 4.4%; anorexia, 6.7%; and diarrhea, 6.7%. Conclusions: This new S-1 and irinotecan combination schedule appeared to be an effective, well-tolerated, and convenient regimen in patients with advanced colorectal cancer as compared with conventional regimens such as FOLFIRI and IRIS. [ABSTRACT FROM AUTHOR]
- Subjects :
- *PATIENT monitoring
*INVESTIGATIONAL drugs
*IRINOTECAN
*ACADEMIC medical centers
*ANTINEOPLASTIC agents
*BIOMARKERS
*BLOOD testing
*COMBINATION drug therapy
*CLINICAL trials
*COLON tumors
*CONFIDENCE intervals
*ELECTROCARDIOGRAPHY
*MEDICAL cooperation
*METASTASIS
*PHYSICAL diagnosis
*RESEARCH
*RESEARCH funding
*SURVIVAL
*TOMOGRAPHY
*DISEASE relapse
*DATA analysis software
*DESCRIPTIVE statistics
*KAPLAN-Meier estimator
*THERAPEUTICS
RECTUM tumors
Subjects
Details
- Language :
- English
- ISSN :
- 11795549
- Issue :
- 7
- Database :
- Academic Search Index
- Journal :
- Clinical Medicine Insights: Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 89427229
- Full Text :
- https://doi.org/10.4137/CMO.S10769