从 LHRH 激动剂转换为促黄体激素释放激素 (LHRH) 拮抗剂治疗进行性去势抵抗性前列腺癌 (CRPC) 的疗效研究
尽管接受了 LHRH 激动剂治疗,但去势抵抗性前列腺癌患者的地加瑞克 II 期单臂研究具有升高的前列腺特异性抗原 (PSA)。
Men with castrate resistant prostate cancer who are switched from a luteinizing hormone-releasing hormone (LHRH) antagonists from a LHRH agonist will experience a fall in prostate-specific antigen (PSA).
研究概览
详细说明
To determine the proportion of patients with castrate resistant Prostate Cancer who have a PSA decline of ≥50% from baseline PSA when switched from an LHRH agonist to an LHRH antagonist.
研究类型
阶段
- 阶段2
联系人和位置
学习地点
-
-
British Columbia
-
Vancouver、British Columbia、加拿大、V5Z4E6
- British Columbia Cancer Agency
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- histologically confirmed adenocarcinoma of the prostate
- currently receiving LHRH agonist
- Anti-androgen oral therapy is permitted but will be discontinued upon enrollment
- PSA > 2 ng/ml
- rising PSA despite LHRH agonist
- patients may or may not have clinical evidence off metastases. If metastases are present, they must be asymptomatic and in bone or lymph node only
- Prior chemotherapy allowed
- ECOG performance status 0-1
Exclusion Criteria:
- Patients with a history of other active malignancies, except: adequately treated non-melanoma skin cancer, superficial bladder cancer, or other solid tumours curatively treated with no evidence of disease for ≥ 3 years.
- Other serious illness, psychiatric or medical condition that would not permit the patient to be managed according to the protocol including: i)Significant cardiovascular condition including but not limited to: uncontrolled hypertension, unstable angina, significant congestive heart failure or myocardial infarction, deep venous thrombosis, pulmonary embolus or cerebrovascular attack within the last 6 months. ii) History of significant neurological disorder that would impair the ability to obtain consent
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Degarelix
Degarelix 240mg subcutaneously loading dose, then 80mg sc every month until disease progression. |
Standard dosing and schedule for administration of degarelix will be used. 240mg s.c. loading dose, 80mg s.c. monthly maintenance dose.
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 |
|---|---|---|
|
50% fall in PSA
大体时间:8 weekly
|
Proportion of patients with castrate resistant prostate cancer (CRPC) who have a PSA decline of ≥50% from baseline when switched from an LHRH agonist to an LHRH antagonist |
8 weekly
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Luteinizing hormone (LH)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
Follicle stimulating hormone (FSH)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
Testosterone (TT)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dehydroepiandrosterone (DHEA)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dehydroepiandrosterone-sulfate (DHEA-S)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
androstenedione (AED)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
|
dihydrotestosterone (DHT)
大体时间:8 weekly
|
Circulating androgen and pituitary hormones will be measured during the course of the study (8 weekly). |
8 weekly
|
合作者和调查者
调查人员
- 首席研究员:Kim N Chi, MD、British Columbia Cancer Agency, Univeristy of British Columbia
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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