首页> 美国卫生研究院文献>British Journal of Cancer >Interleukin-2/interferon-α2a/13-retinoic acid-based chemoimmunotherapy in advanced renal cell carcinoma: results of a prospectively randomised trial of the German Cooperative Renal Carcinoma Chemoimmunotherapy Group (DGCIN)
【2h】

Interleukin-2/interferon-α2a/13-retinoic acid-based chemoimmunotherapy in advanced renal cell carcinoma: results of a prospectively randomised trial of the German Cooperative Renal Carcinoma Chemoimmunotherapy Group (DGCIN)

机译:白细胞介素2 /干扰素-α2a/ 13-视黄酸为基础的化学疗法在晚期肾细胞癌中的作用:德国合作性肾脏癌化学免疫疗法组(DGCIN)的一项前瞻性随机试验结果

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We performed a prospectively randomised clinical trial to compare the efficacy of four subcutaneous interleukin-2-(sc-IL-2) and sc interferon-α2a (sc-IFN-α2a)-based outpatient regimens in 379 patients with progressive metastatic renal cell carcinoma. Patients with lung metastases, an erythrocyte sedimentation rate ⩽70 mm h−1 and neutrophil counts ⩽6000 μl−1 (group I) were randomised to arm A: sc-IL-2, sc-IFN-α2a, peroral 13-cis-retinoic acid (po-13cRA) (n=78), or arm B: arm A plus inhaled-IL-2 (n=65). All others (group II) were randomised to arm C: arm A plus intravenous 5-fluorouracil (iv-5-FU) (n=116), or arm D: arm A plus po-Capecitabine (n=120). Median overall survival (OS) was 22 months (arm A; 3-year OS: 29.7%) and 18 months (arm B; 3-year OS: 29.2%) in group I, and 18 months (arm C; 3-year OS: 25.7%) and 16 months (arm D; 3-year OS: 32.6%) in group II. There were no statistically significant differences in OS, progression-free survival, and objective response between arms A and B, and between arms C and D, respectively. Given the known therapeutic efficacy of sc-IL-2/sc-INF-α2a/po-13cRA-based outpatient chemoimmunotherapies, our results did not establish survival advantages in favour of po-Capecitabine vs iv-5-FU, and in favour of short-term inhaled-IL-2 in patients with advanced renal cell carcinoma receiving systemic cytokines.
机译:我们进行了一项前瞻性随机临床试验,以比较四种基于皮下白介素-2-(sc-IL-2)和皮下干扰素-α2a(sc-IFN-α2a)的门诊方案对379例进行性转移性肾细胞癌患者的疗效。肺转移,红细胞沉降率⩽70mm h -1 和中性粒细胞计数count6000μl -1 的患者(I组)被随机分配到A组:sc-IL -2,sc-IFN-α2a,口服13-顺-视黄酸(po-13cRA)(n = 78)或B组:A组加上吸入的IL-2(n = 65)。所有其他患者(II组)被随机分配到C组:A组加上静脉内5-氟尿嘧啶(iv-5-FU)(n = 116),或D组:A组加上po-卡培他滨(n = 120)。第一组的中位总生存期(OS)为22个月(A组; 3年OS:29.7%)和18个月(B组; 3年OS:29.2%),18天(C组; 3年)。组II:OS:25.7%)和16个月(D组; 3年OS:32.6%)。 A组和B组之间以及C组和D组之间的OS,无进展生存期和客观反应在统计学上无显着差异。鉴于基于sc-IL-2 /sc-INF-α2a/ po-13cRA的门诊化学免疫疗法的已知治疗功效,我们的研究结果并未建立有利于po-Capecitabine相对于iv-5-FU的生存优势,也并未确立生存优势。接受系统细胞因子的晚期肾细胞癌患者的短期吸入IL-2。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号