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首页> 外文期刊>British Journal of Cancer >Protracted venous infusion 5-fluorouracil in combination with subcutaneous interleukin-2 and alpha-interferon in patients with metastatic renal cell cancer: a phase II study
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Protracted venous infusion 5-fluorouracil in combination with subcutaneous interleukin-2 and alpha-interferon in patients with metastatic renal cell cancer: a phase II study

机译:转移性肾细胞癌患者长期静脉输注5-氟尿嘧啶联合皮下白介素2和α-干扰素治疗:II期研究

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Our purpose was to assess the activity of alpha-interferon (IFN-α), interleukin-2 (IL-2) and 5 fluorouracil (5FU) administered by protracted venous infusion (PVI) as opposed to bolus injection. 55 patients with advanced renal cell cancer were treated as follows: IL-2 and IFN-α according to the schedule originally described by Atzpodien, with PVI 5FU 200 mg m–2 day–1 during weeks 5–9. 42 patients (76%) were of moderate or poor prognosis as defined by previous studies. The response rate by intention to treat was 31% (17 of 55, three complete response, 14 partial response; 95% CI = 19–45%) and in evaluable patients (completed one cycle, n = 42), it was 40% (95% CI = 26–57%). In addition, 24% (13 of 55) patients achieved disease stabilization. The overall median survival was 11 months with a 1-year survival of 45%. The median survival for evaluable patients was 18 months with 1- and 2-year survivals of 60% and 40% respectively. The median survival of responding patients was 31 months and the three patients achieving complete response remain progression-free at 14+, 18+ and 23+ months. Evaluable patients with poor prognostic features achieved a response rate of 54% and median survival of 18 months. Toxicity was significant yet manageable with 12 patients unable to complete one cycle due to side-effects and 36% experiencing grade 3–4 toxicities. The three on-treatment deaths were considered unlikely to be due to toxicity. The schedule of IFN-α, IL-2 and PVI 5FU has significant activity in advanced renal cell cancer with manageable toxicity. It is of particular interest that this regimen appears to have high activity in fit patients with poor prognostic features. ? 2000 Cancer Research Campaign
机译:我们的目的是评估与静脉推注相比,延长静脉输注(PVI)所给予的α-干扰素(IFN-α),白介素2(IL-2)和5氟尿嘧啶(5FU)的活性。 55名晚期肾细胞癌患者接受了以下治疗:按照Atzpodien最初描述的时间表治疗IL-2和IFN-α,在5-9周的第1天至第1天服用PVI 5FU 200 mg m-2。根据先前的研究,有42例(76%)患者的中度或较差预后。有意治疗的反应率为31%(55例中有17例,三例完全缓解,部分缓解14例; 95%CI = 19-45%),在可评估患者中(一个周期完成,n = 42),为40%(95%CI = 26-57%)。此外,有24%(55名患者中的13名)患者达到了疾病稳定。总体中位生存期为11个月,一年生存率为45%。可评估患者的中位生存期为18个月,一年和两年生存率分别为60%和40%。有反应的患者的中位生存期为31个月,获得完全缓解的三名患者在14 +,18 +和23+个月仍无进展。可评估的预后不良患者达到了54%的缓解率,中位生存期为18个月。毒性显着但仍可控制,由于副作用和36%的3–4级毒性,有12名患者无法完成一个周期。认为三例治疗中的死亡不太可能是由于毒性所致。 IFN-α,IL-2和PVI 5FU的方案在晚期肾细胞癌中具有显着的活性,且毒性可控。特别令人感兴趣的是,该方案在预后较差的健康患者中似乎具有较高的活性。 ? 2000年癌症研究运动

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