首页> 外文期刊>Gastric cancer: official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association >Combination docetaxel (Taxotere), fluorouracil, and leucovorin (TFL), as first-line chemotherapy in advanced gastric cancer: a Hellenic Cooperative Oncology Group phase II study.
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Combination docetaxel (Taxotere), fluorouracil, and leucovorin (TFL), as first-line chemotherapy in advanced gastric cancer: a Hellenic Cooperative Oncology Group phase II study.

机译:多西他赛(Taxotere),氟尿嘧啶和亚叶酸钙(TFL)的组合,作为晚期胃癌的一线化疗药物:希腊合作肿瘤小组第二阶段研究。

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BACKGROUND: We assessed the efficacy and safety profile of a docetaxel (Taxotere; Sanofi-Aventis, France), fluorouracil (FU), and leucovorin (LV) combination (TFL), as first-line chemotherapy in patients with advanced gastric cancer. METHODS: Fifty-eight patients with advanced gastric cancer were entered in this phase II study. The chemotherapy regimen (TFL) was administered in an outpatient setting as follows: docetaxel 7 mg/m2 on day 1 and FU 50 mg/m2 and LV 30 mg/m2 on days 1 to 3, every 3 weeks for six cycles. RESULTS: On an intent-to-treat basis, 4 complete (7%) and 11 partial responses (19%) were observed, with an objective overall response rate of 26%; in addition, 22 patients (38%) had stable and 15 (26%) had progressive disease. For 6 (10%) patients, response could not be evaluated. Responses were noted at all metastatic sites. With a median follow-up of 55 months, median survival was 9 months; median time to progression, 5.9 months; and median duration of response, 10 months. Toxicity was manageable and no toxic death was reported. Neutropenia was the most frequent severe toxicity and occurred in 30% of the patients. The main non-hematologic toxicities were alopecia (76%), diarrhea (30%), and stomatitis (30%). CONCLUSION: The results of this phase II study seem to indicate that the TFL regimen has moderate activity in patients with advanced gastric cancer, with acceptable toxicity.
机译:背景:我们评估了多西他赛(泰索帝;法国赛诺菲-安万特公司),氟尿嘧啶(FU)和亚叶酸(LV)联合(TFL)作为晚期胃癌患者的一线化疗的疗效和安全性。方法:58名晚期胃癌患者进入了该II期研究。在门诊患者中按以下方式进行化疗方案(TFL):第1天多西他赛7 mg / m2,第1天至第3天FU 50 mg / m2和LV 30 mg / m2,每3周进行6个周期。结果:在意向性治疗的基础上,观察到4例完全缓解(7%)和11例局部缓解(19%),客观总体缓解率为26%;此外,22例(38%)病情稳定,15例(26%)病情进展。对于6名(10%)患者,无法评估反应。在所有转移部位均注意到反应。平均随访55个月,中位生存期为9个月。平均进展时间为5.9个月;和中位持续时间10个月。毒性是可控的,没有毒性死亡的报道。中性粒细胞减少症是最常见的严重毒性反应,发生在30%的患者中。主要的非血液学毒性是脱发(76%),腹泻(30%)和口腔炎(30%)。结论:该II期研究的结果似乎表明,TFL方案在晚期胃癌患者中具有中等活性,并且具有可接受的毒性。

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