Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Istituto Toscano Tumori and Department of Oncology, Transplants and New Technologies in Medicine, University of Pisa, Via Roma, 67, 56126, Pisa, Italy.
Cancer Chemother Pharmacol. 2010 Aug;66(3):559-66. doi: 10.1007/s00280-009-1196-1. Epub 2010 Mar 17.
5-Fluorouracil (5-FU) plus cisplatin (C) can be considered a standard option for advanced gastric cancer (AGC). Irinotecan (Ir) and docetaxel (D) are active agents with no complete cross-resistance with C and 5-FU. Concomitant combination of Ir or D with C and 5-FU is feasible, but with substantial toxicities. A different way to include all active agents in first-line treatment of AGC may be to use them sequentially. We aimed to evaluate the activity and the safety profile of sequential chemotherapy with 5-FU-based doublets with C, Ir and D in the first-line treatment of AGC.
We conducted a phase II study of first-line sequential chemotherapy in metastatic GC. Treatment consisted of 3 cycles of C + infused 5-FU and leucovorin (CFL) followed by 3 cycles of Ir + 5-FU/LV (IrFL) followed by 3 cycles of D + 5-FU/LV (DFL). Primary end-point was response rate.
Forty-six patients were enrolled, median age 60 years, sites of disease (single/multiple) = 9/37, PS 0/1 = 27/19, gastric/gastro-oesophageal junction = 39/7. Median number of cycles was 9. Main grade 3-4 toxicities were neutropenia (37%), febrile neutropenia (2%), diarrhoea (4%), stomatitis (9%). Response rate after the planned 9 cycles was 45% (15 partial and 5 complete responses among 43 evaluable patients). Median PFS and OS: 6.8 and 11.1 months, respectively.
This sequential treatment is feasible with a favourable safety profile and produced encouraging results in terms of activity and efficacy.
5-氟尿嘧啶(5-FU)联合顺铂(C)可被视为晚期胃癌(AGC)的标准治疗选择。伊立替康(Ir)和多西他赛(D)是具有与 C 和 5-FU 无完全交叉耐药性的有效药物。Ir 或 D 与 C 和 5-FU 的联合应用是可行的,但毒性较大。在 AGC 的一线治疗中包含所有有效药物的另一种方法可能是顺序使用它们。我们旨在评估 C、Ir 和 D 联合 5-FU 二联方案在 AGC 一线治疗中的活性和安全性。
我们对转移性 GC 进行了一线序贯化疗的 II 期研究。治疗包括 3 个周期的 C+静脉滴注 5-FU 和亚叶酸(CFL),然后是 3 个周期的 Ir+5-FU/LV(IrFL),然后是 3 个周期的 D+5-FU/LV(DFL)。主要终点是缓解率。
共纳入 46 例患者,中位年龄 60 岁,疾病部位(单发/多发)=9/37,PS 0/1=27/19,胃/胃食管交界处=39/7。中位周期数为 9。主要 3-4 级毒性为中性粒细胞减少(37%)、发热性中性粒细胞减少(2%)、腹泻(4%)、口腔炎(9%)。在计划的 9 个周期后,缓解率为 45%(43 例可评价患者中 15 例部分缓解和 5 例完全缓解)。中位无进展生存期和总生存期分别为 6.8 和 11.1 个月。
这种序贯治疗是可行的,具有良好的安全性,并在活性和疗效方面取得了令人鼓舞的结果。