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临床试验/NCT00714376
NCT00714376
终止
2 期

Phase II Single Center Study of Docetaxel for Clinically Asymptomatic High Risk Prostate Cancer Patients With an Early Rising PSA Following Radical Prostatectomy

CHU de Quebec-Universite Laval1 个研究点 分布在 1 个国家目标入组 6 人2008年5月
干预措施Docetaxel
相关药物Docetaxel

概览

阶段
2 期
干预措施
Docetaxel
疾病 / 适应症
Prostate Cancer
发起方
CHU de Quebec-Universite Laval
入组人数
6
试验地点
1
主要终点
To evaluate the rate of partial and complete biochemical response to 8 cycles of Taxotere in patients with early (<2 years) PSA recurrence after radical prostatectomy with a PSA doubling time of <=9 months.
状态
终止
最后更新
13年前

概览

简要总结

The purpose of this study is to assess the response to Taxotere (docetaxel) chemotherapy given as a primary treatment to patients with early and rapid PSA rising after prostatectomy for high risk disease.

详细描述

Patients with high-risk prostate cancer have a high probability of PSA failure after radical prostatectomy. However, more than half of these patients will remain free of PSA recurrence for more than 10 years. To the contrary, patients with early PSA recurrence and a doubling time less than 10 months have a mortality rate approaching 50% at 10 years despite hormone therapy. Although androgen deprivation therapy (ADT) remains the standard treatment for patients with early and rapidly rising PSA after prostatectomy, this treatment is not curative on the long term for most patients. The recent demonstration of activity of Taxotere (docetaxel) in a high proportion of patients with advanced metastatic disease has stimulated a great interest in it use at an earlier stage of the disease. Recent studies performed in animal models of prostate cancer suggested that the response rate of prostate cancer cells to docetaxel-induced cell death was significantly enhanced by androgen stimulation in AR-positive, androgen-dependent prostate cancer cells (i.e. before ADT). Therefore, this protocol proposes to assess the response rate to primary Taxotere chemotherapy in patients with early and rapid PSA rising after prostatectomy for high risk disease.

注册库
clinicaltrials.gov
开始日期
2008年5月
结束日期
2008年7月
最后更新
13年前
研究类型
Interventional
研究设计
Single Group
性别
Male

研究者

发起方
CHU de Quebec-Universite Laval
责任方
Principal Investigator
主要研究者

Yves Fradet

Urologist-Oncologist

CHU de Quebec-Universite Laval

入排标准

入选标准

  • Diagnosis of prostate adenocarcinoma on a radical prostatectomy.
  • Prior radical prostatectomy within less than 2 years from the time of first PSA rise.
  • Demonstration of biochemical recurrence based on a PSA detectable \>0.03 less than 24 months after radical prostatectomy and confirmed on 2 additional tests.
  • PSA doubling time over three values must be \<= 9 months for PSA \>=0.4 and PSA \<=
  • If PSA is \>10, there is no need for PSA doubling time.
  • Karnofsky performance status (KPS) \>=70%
  • Adequate organ function as defined by hemogram with haemoglobin \>8.0, platelet \>100 000, white blood cell \>3,500, creatinine clearance \>=60 cc/min and normal liver function tests.
  • Neoadjuvant hormone therapy prior to radical prostatectomy is allowed provided that the total duration of therapy did not exceed 6 months.
  • Subjects must have signed an informed consent document stating that they understand the investigational or nature of the proposed treatment.
  • Subjects must be willing and able to comply with scheduled visits, treatment plans, laboratory tests and other procedures.

排除标准

  • Clinical significant cardiac disease (New York Heart Association Class III/IV), or severe debilitating pulmonary disease.
  • Uncontrolled serious active infection.
  • Anticipated duration of life less than 2 years.
  • Less than 5-year history of successful treatment for other cancers or concurrent active non prostate cancer other than non melanoma dermatologic tumors and non-muscle invasive bladder tumors.
  • Peripheral neuropathy \>=2 grade 2
  • Concurrent experimental treatment or involvement in other clinical trials involving drugs.
  • Other severe acute or chronic medical conditions including psychiatric diseases or significant laboratory abnormality requiring further investigation that may cause undue risk for the subject's safety.
  • Subjects who participated in another clinical study/received investigational product within 30 days of screening for this study.

研究组 & 干预措施

Docetaxel

Docetaxel (Taxotere) 75 mg/m² IV every 3 weeks for 8 cycles.

干预措施: Docetaxel

结局指标

主要结局

To evaluate the rate of partial and complete biochemical response to 8 cycles of Taxotere in patients with early (<2 years) PSA recurrence after radical prostatectomy with a PSA doubling time of <=9 months.

时间窗: 3 to 6 months

次要结局

  • To evaluate the response rate to subsequent androgen deprivation therapy in patients not responding and in those having a biochemical recurrence after complete response.(3-6 months)

研究点 (1)

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