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
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
- 否
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
Androgen blockade for 6 months + Radiotherapy 70 Gy
干预措施: Radiotherapy 70 Gy (Radiation)
Arm 1
Androgen blockade for 6 months + Radiotherapy 70 Gy
干预措施: Androgen blockade (Drug)
Arm 2
Androgen blockade for 6 months + Radiotherapy 76 Gy
干预措施: Radiotherapy 76 Gy (Radiation)
Arm 2
Androgen blockade for 6 months + Radiotherapy 76 Gy
干预措施: Androgen blockade (Drug)
Arm 3
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
Abdenour Nabid
Principal Investigator
Université de Sherbrooke
