Capecitabine combined with cisplatin as first-line therapy in Chinese patients with advanced gastric carcinoma-a phase II clinical study.
- Author:
Bing HU
1
;
Ji-Ren YU
;
Zhao-Zhang WEN
;
Yong-Qian SHU
;
Bao-Cheng WANG
;
Hao-Ran YIN
;
Li CHEN
;
Yu-Xian BAI
;
Jun LIANG
;
Li CHEN
;
Ying CHENG
;
Lin SHEN
;
Yun ZHOU
;
Hong-Gang ZHANG
;
Jie LI
;
De-Sen WAN
;
Shuang CHEN
;
Ting-Zhen JIA
;
Mao-Lin JIN
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; adverse effects; therapeutic use; Capecitabine; Cisplatin; administration & dosage; adverse effects; Deoxycytidine; administration & dosage; adverse effects; analogs & derivatives; Female; Fluorouracil; administration & dosage; adverse effects; analogs & derivatives; Follow-Up Studies; Foot Dermatoses; chemically induced; Hand Dermatoses; chemically induced; Humans; Leukopenia; chemically induced; Liver Neoplasms; drug therapy; secondary; Lung Neoplasms; drug therapy; secondary; Lymphatic Metastasis; Male; Middle Aged; Neoplasm Staging; Remission Induction; Stomach Neoplasms; drug therapy; pathology; Survival Rate; Vomiting; chemically induced; Young Adult
- From: Chinese Journal of Oncology 2008;30(12):940-943
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the effectiveness and safety of the combination chemotherapy of capecitabine (X) with fractionated administration of cisplatin (C) in Chinese patients with advanced gastric cancer (AGC).
METHODS141 patients with AGC were enrolled between July 2002 and August 2004. All patients had measurable tumor according to the criteria of RECIST, Karnofsky performance status > or = 60, adequate bone marrow, renal and hepatic functions. Prior radiotherapy or adjuvant chemotherapy was not permitted. Patients received oral administration of capecitabine at a dose of 1000 mg/m(2) twice a day on D1-D14, and intravenous infusion of fractionated cisplatin at a dose of 20 mg/m(2)/day on D1-D5. The regimen was repeated every 3 weeks, totally for 6 cycles.
RESULTSOf the 141 evaluable patients, there were 104 men and 37 women, with a median age of 54 years (range, 23 - 80 years). Metastases before chemotherapy were detected in lymph nodes (46.8%), liver (40.4%), lung (5.7%) and other area (10.6%). The median treatment duration was 6 cycles (range, 3 - 6 cycles). The objective response rate (RR) was 36.2% (51/141). The median follow-up period was 17.5 months. The median time to progress (TTP) was 9.0 months, and the median overall survival (OS) was 12.0 months. The most common treatment-related adverse events (grade 3/4) were: hand-foot syndrome (HFS) (2.1%), leucopenia (0.7%), abnormal alanine transaminase elevation (2.8%). There was no treatment-related death.
CONCLUSIONCapecitabine combined with fractionated cisplatin is highly effective and well tolerated as a first-line treatment for advanced gastric cancer, with comparable results to 5-Fu plus cisplatin combination therapy.