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临床试验/NCT01339962
NCT01339962已完成不适用

Retrospective Analysis Of Progression Free Survival And Overall Survival In A National Cohort Of Patients With Metastatic Renal Cell Carcinoma Treated In Denmark From 2006-2010. DARENCA Study 2.

Pfizer1 个研究点 分布在 1 个国家目标入组 1,073 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
1,073
试验地点
1
主要终点
Overall survival from initiation of first systemic anticancer therapy

研究概览

简要总结

Non-interventional study. Data obtained by patient chart reviews.

Retrospective analysis of progression free survival, time to treatment failure and overall survival in a national cohort of patients with metastatic renal cell carcinoma treated in Denmark from 2006-2010 Safety, prognostic factors, predictive factors and co-morbidity assessed by Charlson Comorbidity Index.

The following drugs will be evaluated: Sunitinib, Sorafenib, Temsirolimus, Everolimus, Aldesleukin, Interferon-alfa-2b.

详细描述

No sampling. All eligible patients will be included.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Metastatic renal cell carcinoma

排除标准

  • 未提供

结局指标

主要结局

Overall survival from initiation of first systemic anticancer therapy

时间窗: 8 months

Progression free survival from initiation of each systemic anticancer therapy separately

时间窗: 8 months

Time to treatment failure from initiation of each systemic anticancer therapy separately

时间窗: 8 months

次要结局

  • Predictive factors(8 months)
  • Assessment of prognostic factors and overall survival for patients not receiving systemic therapy(8 months)
  • Prognostic factors at baseline associated with efficacy (PFS) of each systemic anticancer therapy and overall survival(8 months)
  • Serious Adverse Events: Defined as AEs leading to dose adjustment, treatment interruption/ cessation or death.(8 months)
  • Co-morbidity assessed by Charlson Comorbidity Index(8 months)
  • Combined PFS and OS on sequential treatment(8 months)
  • Assessment of first line immunotherapy´s effect on second line targeted therapy(8 months)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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