SUTENT® In The First Line Treatment Of Renal Cell Carcinoma (SUNIKA)
2010年11月3日 更新者:Pfizer
A Non-Interventional Study With SUTENT® In The First Line Treatment Of Renal Cell Cancer
This non-interventional study includes patients with advanced and/or metastatic renal cell carcinoma who are treated with SUTENT and who did not receive any other systemic therapy before. The aim of the trial is to increase knowledge about quality of life, safety, efficacy and tolerability under conditions of routine use of Sutent. The individual observation period of each patient will be
1 year.
研究概览
详细说明
The Statistical Analysis Plan provides detailed specification of the analysis
研究类型
观察性的
注册 (实际的)
356
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients treated by office-based oncologists, office-based urologists specialized in oncology or hospital-based oncologist/urologists
描述
Inclusion Criteria:
- First-line treatment in patients with metastatic renal cell carcinoma
Exclusion Criteria:
- Any previous systemic therapy of renal cell carcinoma except for adjuvant treatment
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
非干预研究
|
SUNIKA - A Non-Interventional Study With SUTENT® In The First Line Treatment Of Renal Cell Carcinoma
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of Participants With Categorical Best Overall Response
大体时间:Start of Treatment up through 12 Months or Early Discontinuation
|
Best overall reponse based on investigator's disease status assessment.
Complete response(CR)=disappearance of all target lesions.Partial Response(PR)=≥30% decrease in sum of longest dimensions of lesions taking as reference baseline sum longest dimensions.Progressive disease(PD)=≥20% increase in sum of longest dimensions of lesions taking as a reference smallest sum of longest dimensions since treatment start or appearance of ≥1 new lesions.
Stable disease(SD)=neither shrinkage for PR or increase for PD taking as reference smallest sum of longest dimensions since treatment start.
|
Start of Treatment up through 12 Months or Early Discontinuation
|
|
Number of Participants With Objective Response
大体时间:12 Months or Early Discontinuation
|
Objective response (CR or PR) based on investigator's overall objective tumor assessment at final visit according to Response Evaluation Criteria in Solid Tumors (RECIST).
CR was defined as disappearance of all target lesions.
PR was defined as a ≥30% decrease in the sum of the longest dimensions of the target lesions taking as a reference the baseline sum longest dimensions.
|
12 Months or Early Discontinuation
|
|
Time to Progression (TTP)
大体时间:Start of Treatment up through 12 Months or Early Discontinuation
|
TTP = time from date of first dose to date of first recording of PD.
Participants who did not have a recorded PD at any of the visits or at Overall Objective Tumor Assessment at 12 months were treated as censored at the date of the last available follow up for disease response/tumor assessment.
|
Start of Treatment up through 12 Months or Early Discontinuation
|
|
Number of Participants With Eastern Cooperative Oncology Group (ECOG) Performance Status
大体时间:Baseline, 3, 6, 9 and 12 Months
|
ECOG performance status measured on 6 point scale to assess participant's performance status.
0=Fully active, able to carry on all pre-disease activities without restriction; 1=Restricted in physically strenuous activity, ambulatory and able to carry out light or sedentary work; 2=Ambulatory (>50% of waking hours), capable of all self care, unable to carry out any work activities; 3=Capable of only limited self care, confined to bed/chair >50% of waking hours; 4=Completely disabled, cannot carry on any self care, totally confined to bed/chair; 5=Dead.
0=Best status, 5=Worst status
|
Baseline, 3, 6, 9 and 12 Months
|
|
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) Scores
大体时间:Baseline, 3, 6, 9 and 12 Months
|
EORTC QLQ-C30: 5 functional scales (physical, role, cognitive, emotional, and social), a global health status/quality of life (QoL) scale, 3 symptom scales (nausea and vomiting, pain, fatigue) and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea and financial difficulties).
All scales and single-item measures range=0 to 100.
High score for a functional scale=high/healthy level of functioning.
High score for global health status/QoL=high QoL.
High score for symptom scale/single item=high level of symptomatology/problems
|
Baseline, 3, 6, 9 and 12 Months
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
赞助
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2007年2月1日
初级完成 (实际的)
2009年9月1日
研究完成 (实际的)
2009年9月1日
研究注册日期
首次提交
2007年4月13日
首先提交符合 QC 标准的
2007年4月13日
首次发布 (估计)
2007年4月16日
研究记录更新
最后更新发布 (估计)
2010年11月16日
上次提交的符合 QC 标准的更新
2010年11月3日
最后验证
2010年11月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.