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A Phase II Trila of Sunitinib Schedule 4/2 vs. Shedule 2/1 as First Line Therapy in Metastatic Renal Cell Carcinoma.

2016年2月27日 更新者:Jun Guo、Peking University Cancer Hospital & Institute

A Randomized Phase II Trila of Sunitinib Four-weeks on/Two-weeks Off Versus Two-weeks on/One-week Off as First Line Therapy in Metastatic Renal Cell Carcinoma.

Sunitinib given at 50 mg/day on schedule 4/2 (4 weeks on treatment, 2 weeks off) is the standard care for first-line treatment of metastatic renal cell carcinoma, but the schedule was reported with a high rate of dose reduction and dose discontinuation because of the safety profile. So investigators conducte this randomized, multi-center phase II study to determine whether a sunitinib regimen of 50 mg/day 2-weeks on/1-week off could provide the same efficacy in terms of progression-free survival, objective response, and overall survival, while reducing drug-related toxicity.

研究概览

地位

未知

干预/治疗

详细说明

Sunitinib given at 50 mg/day on schedule 4/2 (4 weeks on treatment, 2 weeks off) is the standard care for first-line treatment of metastatic renal cell carcinoma, but the schedule was reported with a high rate of dose reduction and dose discontinuation because of the safety profile. Sunitinib 50mg/day on schedule 2/1 (2 weeks on treatment, 1 weeks off) was reported to be associated with significantly decrease toxicities in patients who initially experienced grade 3 or greater toxicity on the schedule 4/2 and could extend treatment duration considerably. Through this research, we would like to explore whether the schedule 2/1 of sunitinib 50 mg/day as first line therapy could provide the same efficacy as standard schedule 4/2 in terms of progression-free survival, objective response, and overall survival, while reducing drug-related toxicity in metastatic renal cell carcinoma patients.

研究类型

介入性

注册 (预期的)

80

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Chuanliang Cui, MD
  • 电话号码:0086-10-88196951
  • 邮箱1008ccl@163.com

研究联系人备份

  • 姓名:Jun Guo, MD,PHD
  • 电话号码:0086-10-88196317
  • 邮箱guoj307@126.com

学习地点

    • Beijing
      • Beijing、Beijing、中国、100142
        • 招聘中
        • Beijing Cancer Hospital
        • 接触:
          • Chuanliang Cui, MD
          • 电话号码:0086-10-88196951
          • 邮箱1008ccl@163.com
        • 接触:
        • 首席研究员:
          • Jun Guo, MD,PHD
      • Beijing、Beijing、中国、100034
        • 尚未招聘
        • Peking University First Hospital
        • 接触:
        • 首席研究员:
          • Zhisong He, MD
      • Beijing、Beijing、中国、100021
        • 尚未招聘
        • Chinese acadamy of medical science cancer institute & hospital
        • 接触:
        • 首席研究员:
          • Changling Li, MD
    • Guangdong
      • Guangzhou、Guangdong、中国、510060
        • 尚未招聘
        • Sun Yat-sen University Cancer Center
        • 接触:
        • 首席研究员:
          • Fangjian Zhou, MD
    • Shanghai
      • Shanghai、Shanghai、中国、200032
        • 尚未招聘
        • Cancer Hospital, FuDan University
        • 接触:
          • Dingwei Ye, MD
          • 电话号码:0086-21-64175590
          • 邮箱dwye@163.com
        • 首席研究员:
          • Dingwei Ye, MD
    • Tianjin
      • Tianjin、Tianjin、中国、300060
        • 尚未招聘
        • Tianjin Medical University Cancer Institute & Hospital
        • 接触:
        • 首席研究员:
          • Xin Yao, MD

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

18年 至 75年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age≥18 years, ≤75 years, male or female
  • Advanced renal cell carcinoma is diagnosed histologically or pathologically
  • Treatment naive at diagnosed
  • At least one measurable tumor lesion (Response Evaluation Criteria In Solid Tumors)
  • Eastern Cooperative Oncology Group(ECOG) performance scale is 0 or 1
  • The expected life span is ≥12 weeks
  • No contraindications for targeted therapy, with enough liver function and renal function and normal ECG recording Peripheral hemogram: neutrophil≥1.5×109/L, Plt≥100×109/L, Hgb≥90g/L Renal function: serum creatinine≤1.5 folds the upper limit of normal (ULN) For patients with non-metastatic liver dysfunction:alanine aminotransferase and aspartate aminotransferase≤2.5 ULN, For patients with metastatic liver dysfunction: alanine aminotransferase and aspartate aminotransferase≤5 ULN
  • The patients participate voluntarily and have signed the informed consent form

Exclusion Criteria:

  • Patients who have received any systemic therapy including targeted therapy,immunotherapy,chemotherapy etc at diagnosed.
  • Pregnant and lactating women, or female patients of child-bearing age without taking contraceptive measures
  • Patients with severe acute infection without being controlled effectively or having pyogenic and chronic infections with persistently unhealed wounds
  • Past history of serious heart diseases, including: cardiac function classification ≥NYHA class II, unstable angina pectoris, myocardial infarction, arrhythmia requiring anti-arrhythmic drug therapy (excluding β-blockers or digoxin), and uncontrolled hypertension
  • Patients with a history of HIV infection or active phase of chronic hepatitis B/C
  • negative imaging examination result 4 weeks prior to enrollment)
  • Epilepsy patients requiring drug therapy (e.g. steroids or antiepileptic drugs)
  • A history of allogeneic organ transplantation

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

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Sunitinib 50mg/day schedule 4/2
Sunitinib 50mg/day 4 weeks on/2 weeks off per 6 weeks till disease progression or intolerable toxicity.
altenative schedules of sunitinib as first line therapy in metastatic renal cell carcinoma patients.
其他名称:
  • 索坦
实验性的:Sunitinib 50mg/day schedule 2/1
Sunitinib 50mg/day 2 weeks on/1 week off per 6 weeks till disease progression or intolerable toxicity.
altenative schedules of sunitinib as first line therapy in metastatic renal cell carcinoma patients.
其他名称:
  • 索坦

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
progress-free survival (PFS)
大体时间:2 years
Time from enrollment to the dates of disease progression,death from any cause or last tumor assessment reported between date of first patient enrollment until March 2017 cut off date
2 years

次要结果测量

结果测量
大体时间
The percentage of patients who can get complete response, partial response.
大体时间:2 years
2 years

其他结果措施

结果测量
大体时间
不良事件数
大体时间:1年
1年

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。

调查人员

  • 首席研究员:Jun Guo, MD,PHD、Peking University Cancer Hospital & Institute

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

2015年3月1日

初级完成 (预期的)

2017年3月1日

研究完成 (预期的)

2017年3月1日

研究注册日期

首次提交

2015年3月20日

首先提交符合 QC 标准的

2015年3月24日

首次发布 (估计)

2015年3月25日

研究记录更新

最后更新发布 (估计)

2016年3月1日

上次提交的符合 QC 标准的更新

2016年2月27日

最后验证

2016年2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.

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