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Gan To Kagaku Ryoho ; 32(9): 1319-22, 2005 Sep.
Article in Japanese | MEDLINE | ID: mdl-16184932

ABSTRACT

We performed a pilot study of combination chemotherapy with TS-1 and cisplatin for highly advanced gastric cancer. From June 2002, 12 patients with multiple liver metastases, carcinomatous lymphangitis or peritoneal dissemination, were enrolled in the study. TS-1 was administered at a daily dose on day 1-21 and an intermediate-dose of cisplatin (60 mg/m2) was administered on day 8. The combination was repeated in a 5-week cycle. The median administered cycles were three (one to eight). An objective response was obtained in 9 cases (75.0%) of primary sites and 6 cases of metastatic sites. No severe hematological toxicity occurred, and grade 3 stomatitis (in one case) and vomiting (in two cases) occurred as non-hematological toxicities. The improvement of clinical symptoms such as appetite loss and abdominal discomfort was obtained in 9 of 10 cases. The median survival time is 244 days. The TS-1/CDDP regimen had almost no survival benefits, but may induce relief of symptoms due to cancer and better quality of life.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Signet Ring Cell/drug therapy , Stomach Neoplasms/drug therapy , Administration, Oral , Adult , Aged , Carcinoma, Signet Ring Cell/surgery , Cisplatin/administration & dosage , Combined Modality Therapy , Drug Administration Schedule , Drug Combinations , Female , Humans , Male , Middle Aged , Oxonic Acid/administration & dosage , Paclitaxel/administration & dosage , Pilot Projects , Pyridines/administration & dosage , Quality of Life , Stomach Neoplasms/surgery , Tegafur/administration & dosage
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