Abstract | OBJECTIVES: To evaluate the efficacy and safety of capecitabine in patients with advanced or recurrent gastric cancer, we conducted a pilot phase II study in Japan. METHODS: Patients with advanced or recurrent gastric cancer were given oral capecitabine 828 mg/m(2) twice daily for 3 weeks, followed by 1 week of no treatment. Two or more cycles were administered. From July 1996 to December 1997, 32 patients were enrolled in the study. The response to capecitabine was evaluated in 31 patients, excluding 1 found to be ineligible. RESULTS: The overall response rate was 19.4% (6/31, 95% confidence interval: 7.5-37.5%). The median duration of response was 124.5 days, the median time to disease progression 85.0 days, and the median survival time 247.5 days. Drug-related adverse events of grade 3 or higher were infrequent: in 2 patients (6.3%) total bilirubin concentration increased, and 1 patient (3.1%) each had elevation of GOT, anemia, lymphopenia, increased creatinine, and hand-foot syndrome. No patient had gastrointestinal toxicity of grade 3 or higher. CONCLUSION:
|
Authors | Wasaburo Koizumi, Katsunori Saigenji, Shigeki Ujiie, Masanori Terashima, Yu Sakata, Tetsuo Taguchi, Clinical Study Group of Capecitabine |
Journal | Oncology
(Oncology)
Vol. 64
Issue 3
Pg. 232-6
( 2003)
ISSN: 0030-2414 [Print] Switzerland |
PMID | 12697963
(Publication Type: Clinical Trial, Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright 2003 S. Karger AG, Basel |
Chemical References |
- Antimetabolites, Antineoplastic
- Deoxycytidine
- Capecitabine
- Fluorouracil
|
Topics |
- Administration, Oral
- Adult
- Aged
- Antimetabolites, Antineoplastic
(administration & dosage, therapeutic use)
- Capecitabine
- Deoxycytidine
(administration & dosage, analogs & derivatives, therapeutic use)
- Drug Administration Schedule
- Female
- Fluorouracil
(analogs & derivatives)
- Humans
- Japan
- Male
- Middle Aged
- Neoplasm Recurrence, Local
(drug therapy)
- Pilot Projects
- Stomach Neoplasms
(drug therapy, pathology)
- Treatment Outcome
|