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Japanese Journal of Clinical Oncology 2007 37(12):936-941; doi:10.1093/jjco/hym123
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© The Author (2008). Published by Oxford University Press. All rights reserved

Docetaxel Monotherapy as a Second-line Treatment after Failure of Fluoropyrimidine and Platinum in Advanced Gastric Cancer: Experience of 154 Patients with Prognostic Factor Analysis

Jae-Cheol Jo, Jae-Lyun Lee, Min-Hee Ryu, Sun Jin Sym, Sung Sook Lee, Heung Moon Chang, Tae Won Kim, Jung Shin Lee and Yoon-Koo Kang

Division of Oncology, Department of Internal Medicine, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea

For reprints and all correspondence: Yoon-Koo Kang, Division of Oncology, Department of Internal Medicine, University of Ulsan College of Medicine, Asan Medical Center, 388-1 Poongnap-2dong, Songpa-gu, Seoul 138-736, South Korea. E-mail: ykkang{at}amc.seoul.kr

Received June 7, 2007; accepted August 4, 2007

Objective: To investigate the efficacy and safety of docetaxel monotherapy as salvage chemotherapy for advanced gastric cancer (AGC) in clinical practice and to determine the prognostic factors in these patients.

Methods: We retrospectively reviewed the medical records of patients with AGC for whom fluoropyrimidine and platinum had previously failed and who had received docetaxel salvage monotherapy between December 2000 and March 2006. Docetaxel was administered at a dose of 75 mg/m2 intravenously every 3 weeks with dexamethasone prophylaxis.

Results: A total of 154 patients received 583 cycles of docetaxel with a median of three cycles per patient (range 1–10). The median age was 54 years (range 27–75 years). The objective response rate of 86 patients with measurable lesions was 14%, with 1 complete response and 11 partial responses, with a median response duration of 5.6 months. An additional 25 patients achieved stable disease. The median time to progression (TTP) for all patients was 2.6 months [95% confidence interval (CI), 2.2–2.9] and the median overall survival (OS) from the start of docetaxel chemotherapy was 7.2 months (95% CI, 5.9–8.5). The chemotherapy was generally well tolerated. Multivariate analysis showed that the Eastern Cooperative Oncology Group (ECOG) performance status (0 or 1 versus 2) was an independent prognostic factor for both TTP and OS. Disease status indicative of a relatively small tumor burden (resected metastatic or recurrent tumor) was a predictor for better TTP and good differentiation of the tumor was a predictor for better OS.

Conclusion: Docetaxel 75 mg/m2 is relatively active and tolerable as a second-line salvage treatment after failure of fluoropyrimidine and platinum in general clinical practice for AGC.

Key Words: docetaxel • advanced gastric cancer • salvage chemotherapy


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