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Phase II study of docetaxel, oxaliplatin, and S-1 therapy in patients with metastatic gastric cancer

Background Although the docetaxel, 5-fluorouracil, and cisplatin triplet has yielded significant improvements in time to progression, overall survival, and overall response rate, the high incidence of severe adverse events limits the use of the docetaxel, 5-fluorouracil, and cisplatin triplet. To ov...

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Published in:Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2016-04, Vol.19 (2), p.579-585
Main Authors: Kim, Hyeong Su, Ryu, Min-Hee, Zang, Dae Young, Ryoo, Baek-Yeol, Yang, Dae Hyun, Cho, Ji Woong, Lim, Man Sup, Kim, Min-Jeong, Han, Boram, Choi, Dae Ro, Kim, Jung Han, Jung, Joo Young, Song, Hunho, Park, Choong Kee, Kang, Yoon-Koo
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Language:English
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Summary:Background Although the docetaxel, 5-fluorouracil, and cisplatin triplet has yielded significant improvements in time to progression, overall survival, and overall response rate, the high incidence of severe adverse events limits the use of the docetaxel, 5-fluorouracil, and cisplatin triplet. To overcome this limitation, we evaluated the efficacy and safety of the combination of docetaxel, oxaliplatin, and S-1 for the treatment of metastatic gastric cancer. Methods Chemotherapy-naive patients with pathologically proven unresectable recurrent or metastatic gastric adenocarcinoma were assessed for eligibility. Docetaxel at 52.5 mg/m 2 and oxaliplatin at 105 mg/m 2 were administered intravenously on day 1, and S-1 was administered orally at 80 mg/m 2 on days 1–14 of every 21-day cycle. Results Forty-four patients (median age 54.5 years) were enrolled. All patients had metastatic disease. A total of 340 cycles of chemotherapy were administered (median of eight cycles per patient; range 1–36 cycles). Toxicities were evaluated in 43 patients, and the responses were evaluated in 40 patients. Major toxicities included grade 3/4 neutropenia (37.2 %) and leukopenia (27.9 %). The overall response rate was 54.5 % [95 % confidence interval (CI) 40.1–68.3 %] in the intention-to-treat population. The median progression-free survival and overall survival were 7.6 months (95 % CI 6.2–9.0 months) and 12.0 months (95 % CI 6.9–17.2 months), respectively. Conclusion These data suggest that the docetaxel, oxaliplatin, and S-1 combination regimen is effective and relatively well tolerable, and it seems to have potential to be a reasonable therapeutic strategy in patients with metastatic or recurrent gastric cancer.
ISSN:1436-3291
1436-3305
DOI:10.1007/s10120-015-0503-2