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Gemcitabine and protracted 5-FU for advanced pancreatic cancer. A phase II study.

机译:吉西他滨和延长的5-FU治疗晚期胰腺癌。 II期研究。

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BACKGROUND/AIMS: Although chemotherapy in advanced pancreatic cancer procures dismal results, both 5-fluorouracil and gemcitabine have shown a modest activity. We report a phase II study of gemcitabine combined with protracted 5-fluorouracil. METHODOLOGY: Gemcitabine was given at 1000 mg/m2/week intravenously, in combination with concomitant 5-fluorouracil 200 mg/m2/day as a protracted venous infusion, both 3 out of 4 weeks in patients with locally advanced or metastatic pancreatic adenocarcinoma. Twenty-nine patients were enrolled, among whom 27 were metastatic. Response rate, overall and progression-free survival were endpoints, as well as tolerance and clinical benefit. RESULTS: We observed 3 (10%) partial responses, and 12 (42%) stabilizations within which the median disease control was 5.6 months. The median progression-free and overall survivals were 2.8 and 4 months, respectively. A clinical benefit was observed in 39% of patients. Myelosuppression was the main toxicity, but no grade 4 was observed. Other toxicities were mild. CONCLUSIONS: This combination chemotherapy was well tolerated in advanced pancreatic cancer patients.
机译:背景/目的:尽管晚期胰腺癌的化疗取得了令人沮丧的结果,但5-氟尿嘧啶和吉西他滨均显示出适度的活性。我们报告了吉西他滨联合长期使用的5-氟尿嘧啶的II期研究。方法:吉西他滨静脉给药为1000 mg / m2 /周,并伴随长期静脉输注200 mg / m2 / day的5-氟尿嘧啶,在局部晚期或转移性胰腺腺癌患者中,每4周需3周。入组患者29例,其中转移性27例。缓解率,总体生存率和无进展生存率是终点,还有耐受性和临床获益。结果:我们观察到3(10%)部分反应和12(42%)稳定,其中疾病控制中位数为5.6个月。中位无进展生存期和总生存期分别为2.8和4个月。在39%的患者中观察到临床获益。骨髓抑制是主要的毒性反应,但未观察到4级。其他毒性轻微。结论:晚期胰腺癌患者对这种联合化疗耐受良好。

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