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临床试验/NCT00223145
NCT00223145进行中(未招募)3 期

Randomized, Multicentre, Phase III Study in Patients with Intermediate-risk T1 T2 Prostate Adenocarcinomas, to Verify the Role of Six Months of Total Androgen Blockade for Two Dosage Levels of Prostate Radiation Therapy (70 Gy and 76 Gy) Versus Prostate Radiation Therapy Alone At 76 Gy

Abdenour Nabid1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2000年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
600
试验地点
1
主要终点
Interval before biochemical failure

研究概览

简要总结

The hypothesis of the proposed study would be that, due to the six months of total androgen blockade, which would include neoadjuvant hormonal therapy for four months and concomitant hormonal therapy for two months with irradiation, the investigators could reduce local failure rates for these two dosage levels, namely 70 Gy and 76 Gy. Since increasing the dose to the prostate also seems to reduce local relapse rates, the results of the two hormonal therapy groups would be compared with the results of prostate irradiation at doses of 76 Gy. This study would verify the possibility of compensating a six Gy dosage increase of radiation therapy with six months of hormonal therapy between the 70 Gy and 76 Gy groups who received hormonal therapy, and also match these results with a dose escalation to the prostate of 76 Gy. In the future, this could result in more therapeutic choices, such as reducing the doses of radiation therapy and, consequently, its related complications, if hormonal therapy proves to be beneficial; or rather, to continue in the direction of dose escalation for this intermediate-risk patient group, everything being correlated to the side effects of hormonal therapy and irradiation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Patients with stage T1 or T2 untreated adenocarcinoma of the prostate, with a Gleason score that is less than or equal to 6, as well as a prostate-specific antigen (PSA) between 10-20 (intermediate risk) or patients with stage T1 or T2 untreated adenocarcinoma of the prostate, with a Gleason score that is equal to 7, as well as a PSA equal to or less than 20 (intermediate risk).
  • Performance status score of 0-1
  • Patients must sign a consent form before starting the study.
  • No evidence of regional disease
  • Patients with a previous history of cancer are eligible on the condition that they have been disease-free for more than five years.
  • Non-invasive epidermoid cancers of the skin are eligible.
  • The patient must be available for treatments and follow-up visits.
  • No evidence of metastatic disease, confirmed by a negative bone scan.

排除标准

  • Severe medical or psychiatric problems that may compromise study compliance
  • Chronic hepatic disease; abnormal hepatic function, i.e. aspartate aminotransferase and alanine aminotransferase > 1.5 times the upper normal limit.

研究组 & 干预措施

Arm 1

Experimental

Androgen blockade for 6 months + Radiotherapy 70 Gy

干预措施: Radiotherapy 70 Gy (Radiation)

Arm 1

Experimental

Androgen blockade for 6 months + Radiotherapy 70 Gy

干预措施: Androgen blockade (Drug)

Arm 2

Experimental

Androgen blockade for 6 months + Radiotherapy 76 Gy

干预措施: Radiotherapy 76 Gy (Radiation)

Arm 2

Experimental

Androgen blockade for 6 months + Radiotherapy 76 Gy

干预措施: Androgen blockade (Drug)

Arm 3

Active Comparator

Radiotherapy alone with 76 Gy

干预措施: Radiotherapy 76 Gy (Radiation)

结局指标

主要结局

Interval before biochemical failure

时间窗: 10 years

次要结局

  • Toxicity of irradiation(10 years)
  • Survival(10 years)

研究者

发起方
Abdenour Nabid
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Abdenour Nabid

Principal Investigator

Université de Sherbrooke

研究点 (1)

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