首页> 外文期刊>BJU international >Overall survival in patients with metastatic renal cell carcinoma initially treated with bevacizumab plus interferon-alpha2a and subsequent therapy with tyrosine kinase inhibitors: a retrospective analysis of the phase III AVOREN trial.
【24h】

Overall survival in patients with metastatic renal cell carcinoma initially treated with bevacizumab plus interferon-alpha2a and subsequent therapy with tyrosine kinase inhibitors: a retrospective analysis of the phase III AVOREN trial.

机译:最初用贝伐单抗加干扰素-α2a治疗并随后用酪氨酸激酶抑制剂治疗的转移性肾细胞癌患者的总生存期:III期AVOREN试验的回顾性分析。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

OBJECTIVE: * To retrospectively evaluate the effect of subsequent tyrosine kinase inhibitors (TKIs) after first-line bevacizumab + interferon-alpha2a (IFN) or IFN + placebo in the phase III AVOREN (Avastin and Roferon in Renal Cell Carcinoma) trial. PATIENTS AND METHODS: * A total of 649 patients with untreated metastatic renal cell carcinoma (mRCC) were randomized to receive IFN (9 MIU three times a week for up to 1 year) in combination with bevacizumab (10 mg/kg every 2 weeks) or placebo until disease progression. * The protocol allowed the use of any post-protocol anti-cancer therapy for patients with progressive disease or those in whom the trial therapy was discontinued. Data regarding the timing and type of subsequent therapy were recorded and overall survival (OS) analysed. RESULTS: * Patients were randomized to bevacizumab + IFN (n= 327) or IFN + placebo (n= 322); 180 (55%) patients in the bevacizumab + IFN, and 202 (63%) in the IFN + placebo arm, received post-protocol anti-cancer therapy. * TKIs were the most common post-protocol therapy, received by 113 (35%) and 120 (37%) patients in the bevacizumab + IFN and IFN + placebo arms, respectively. * The median OS in patients who received any subsequent TKI was 38.6 months in the bevacizumab + IFN arm and 33.6 months in IFN + placebo arm [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.56-1.13; P= 0.203]. In an additional retrospective analysis that censored patients who received subsequent TKIs, median OS was 25.0 and 20.7 months, respectively, in the bevacizumab + IFN and IFN + placebo arms (HR, 0.84; 95% CI, 0.67-1.05; P= 0.123). CONCLUSIONS: * These retrospective exploratory data of sequential bevacizumab + IFN followed by TKIs in patients able to receive multiple lines of therapy suggest that sequential therapy could be a promising approach to improve patient outcomes in mRCC.
机译:目的:*回顾评估一线贝伐单抗+干扰素-α2a(IFN)或IFN +安慰剂一线后的后续酪氨酸激酶抑制剂(TKIs)在III期AVOREN(肾细胞癌中的Avastin和Roferon)试验中的作用。患者和方法:*总共649例未经治疗的转移性肾细胞癌(mRCC)患者随机接受IFN(每周3次,共9次MIU,最多1年)与贝伐单抗联合(每2周10 mg / kg)或安慰剂直至疾病进展。 *该协议允许对患有进行性疾病的患者或中止试验治疗的患者使用任何协议后抗癌治疗。记录有关后续治疗的时间和类型的数据,并分析总生存期(OS)。结果:*患者被随机分为贝伐单抗+ IFN(n = 327)或IFN +安慰剂(n = 322);贝伐单抗+干扰素治疗的180名患者(55%),干扰素+安慰剂治疗组的202名患者(63%)接受了方案后抗癌治疗。 * TKI是最常见的方案后治疗,贝伐单抗+ IFN和IFN +安慰剂组分别有113(35%)和120(37%)位患者接受。 *接受贝伐单抗+干扰素治疗的患者接受TKI的中位OS为38.6个月,接受干扰素+安慰剂治疗的患者中位OS为33.6个月[危险比(HR)为0.80; 95%置信区间(CI),0.56-1.13; P = 0.203]。在一项额外的回顾性分析中,对接受后续TKI的患者进行了检查,贝伐单抗+ IFN和IFN +安慰剂组的中位OS分别为25.0和20.7个月(HR,0.84; 95%CI,0.67-1.05; P = 0.123) 。结论:*这些循序的贝伐单抗+ IFN联合TKI的回顾性探索性数据,对能够接受多系治疗的患者表示,序贯治疗可能是改善mRCC患者预后的有前途的方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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