Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang 410-769, Korea.
Br J Cancer. 2013 Sep 17;109(6):1420-7. doi: 10.1038/bjc.2013.479. Epub 2013 Aug 20.
S-1 is an oral fluoropyrimidine that mimics infusional 5-fluorouracil. The aim of this phase II trial was to explore the clinical efficacy of the triplet regimen TIROX, which consists of S-1, irinotecan and oxaliplatin.
Forty-two chemo-naive patients with metastatic colorectal cancer (mCRC) were planned to be enrolled and be treated with irinotecan 150 mg m(-2) followed by oxaliplatin 85 mg m(-2) on day 1 and S-1 80 mg m(-2) per day from day 1 to 14 every 3 weeks. Polymorphisms in the UGT1A1, UGT1A6, UGT1A7 and CYP2A6 genes were analysed.
Between July 2007 and February 2008, 43 patients were enrolled. An objective response was noted in 29 patients (67.4%, 95% confidence interval: 53.4-81.4), of which 2 achieved durable complete responses. The median progression-free survival was 10.0 months and the median overall survival was 19.2 months. Significant grade 3 or 4 adverse events were neutropenia (45.2%), febrile neutropenia (9.5%), diarrhoea (7.1%) and vomiting (9.5%). Increased gastrointestinal toxicities were associated with the presence of UGT1A62 or UGT1A73 and an improved tumour response was noted in those without variant alleles of CYP2A6 or UGT1A1*60.
The combination of S-1, irinotecan and oxaliplatin showed favourable efficacy and tolerability in untreated patients with mCRC.
S-1 是一种模拟持续输注氟尿嘧啶的口服氟嘧啶类药物。本 II 期试验旨在探索 S-1、伊立替康和奥沙利铂三联方案 TIROX 的临床疗效,该方案由 S-1、伊立替康和奥沙利铂组成。
计划招募 42 例初治转移性结直肠癌(mCRC)患者,接受伊立替康 150mg/m2 静脉滴注,随后奥沙利铂 85mg/m2 静脉滴注,第 1 天;S-1 80mg/m2,每天 1 次,从第 1 天到第 14 天,每 3 周 1 次。分析 UGT1A1、UGT1A6、UGT1A7 和 CYP2A6 基因的多态性。
2007 年 7 月至 2008 年 2 月期间,共招募 43 例患者。29 例(67.4%,95%置信区间:53.4-81.4)患者观察到客观缓解,其中 2 例获得持久完全缓解。中位无进展生存期为 10.0 个月,中位总生存期为 19.2 个月。显著的 3 级或 4 级不良事件有中性粒细胞减少症(45.2%)、发热性中性粒细胞减少症(9.5%)、腹泻(7.1%)和呕吐(9.5%)。胃肠道毒性增加与 UGT1A62 或 UGT1A73 有关,而 CYP2A6 或 UGT1A1*60 无变异等位基因的患者肿瘤反应改善。
S-1、伊立替康和奥沙利铂联合治疗初治 mCRC 患者疗效良好,耐受性好。