Jeung H-C, Rha S Y, Cho B C, Yoo N C, Roh J K, Roh W J, Chung H C, Ahn J B
Cancer Metastasis Research Center, Yonsei University College of Medicine, Seoul, Korea.
Br J Cancer. 2006 Dec 18;95(12):1637-41. doi: 10.1038/sj.bjc.6603468. Epub 2006 Nov 14.
This is the first phase II study of S-1 monotherapy for patients with metastatic colorectal cancer after failure of both irinotecan- and oxaliplatin-containing regimens. The initial dose of S-1 was 35 mg m-2, administered twice daily for 14 days every 3 weeks. Treatment was repeated until the occurrence of disease progression. Twenty-eight patients were enrolled. S-1 was administered to 21 patients as third-line therapy and to the remaining seven patients as fourth-line therapy. Of 26 evaluable patients, the overall response rate was 14.3% (95% CI, 0.4-28.1), and the disease control rate was 42.9% (95% CI, 23.3-62.4). With a median follow-up period of 227 days, median time to progression and overall survival duration were 91 and 414 days, respectively. The 1-year survival rate of all patients was 60.7%. There was no grade 4 toxicity. Grade 3 haematological toxicities were documented only in two patients. In conclusion, S-1 shows potential as a salvage regimen in heavily pretreated colorectal cancer patients. The twice-daily dose of 35 mg m-2 was well tolerated and can be used in designing further combination chemotherapy.
这是一项关于S-1单药治疗含伊立替康和奥沙利铂方案治疗失败后的转移性结直肠癌患者的II期研究。S-1的初始剂量为35mg/m²,每3周每日两次给药,共14天。治疗重复进行直至疾病进展。共入组28例患者。21例患者接受S-1作为三线治疗,其余7例患者接受S-1作为四线治疗。在26例可评估患者中,总缓解率为14.3%(95%CI,0.4-28.1),疾病控制率为42.9%(95%CI,23.3-62.4)。中位随访期为227天,中位疾病进展时间和总生存时间分别为91天和414天。所有患者的1年生存率为60.7%。无4级毒性。仅2例患者记录有3级血液学毒性。总之,S-1在经过大量预处理的结直肠癌患者中显示出作为挽救方案的潜力。每日两次35mg/m²的剂量耐受性良好,可用于设计进一步联合化疗。