Effectiveness of Focal Therapy in Men With Prostate Cancer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 356
- 试验地点
- 6
- 主要终点
- Quality of life (superiority) measured with Functional Assessment of Cancer Therapy-Prostate questionnaire
研究概览
简要总结
In the Netherlands, most men with prostate cancer (PCa) are treated with radical whole-gland treatment, i.e. prostatectomy or radiotherapy. The burden of complications such as incontinence and erectile dysfunction associated with radical treatment is considerable. A recent systematic review by our group has shown that focal therapy of PCa seems to reduce the burden of treatment side-effects in men with intermediate-risk disease, maintaining their quality of life without compromising oncological effectiveness. The costs of side effects that can be prevented are estimated at €5456 per patient, resulting in total expected cost savings of about €22 million per year in The Netherlands. Furthermore, exploration of the benefit-risk balance under patients showed that they are willing to sacrifice some survival for an improvement in quality of life (QoL).
Focal therapy comprises a modern alternative to selectively treat a specific part of the prostate while preserving the rest of the gland. There is, however, a lack of high-quality evidence, and numerous papers therefore recommend to perform a multicenter randomized controlled trial (RCT). The RCT should have long-term follow-up, predefined assessment of cancer-specific and health-related QoL outcome measures, and economic evaluations to inform policymakers regarding cost-effectiveness. This RCT on focal therapy versus usual care is urgently needed to enable focal therapy to overgrow the experimental status, provide the evidence needed for guidelines, and make this available for selected patients who benefit from this strategy. Because of its promising results in other countries, focal therapy is increasingly requested by patients, but due to the lack of high-quality evidence, it is not reimbursed yet. This has been designated by both the PCa patient support group and physicians as a failure of both the market and the funding agencies. The investigators, therefore, aim to perform a high-quality multi-center RCT to provide the evidence needed to decide on reimbursement and implementation of focal therapy in patients with intermediate-risk, unilateral clinically localized PCa in the Netherlands.
详细描述
In the Netherlands, most men with PCa are treated with radical whole-gland treatment, i.e. prostatectomy or a form of radiotherapy. The burden of complications such as incontinence and erectile dysfunction associated with radical treatment is considerable.
A recent systematic review by our group has shown that focal therapy of PCa seems to reduce the burden of treatment side-effects in men with intermediate-risk disease, maintaining their quality of life without compromising oncological effectiveness. The costs of side-effects that can be prevented are estimated at €5456 per patient, resulting in total expected cost savings of about €22 million per year in The Netherlands. Furthermore, exploration of the benefit-risk balance under patients showed that they are willing to sacrifice some survival for an improvement in quality of life (QoL).
Focal therapy comprises a modern alternative to selectively treat a specific part of the prostate while preserving the rest of the gland. There is, however, a lack of high-quality evidence, and numerous papers therefore recommend to perform a multicenter randomized controlled trial (RCT). The RCT should have long-term follow-up, predefined assessment of cancer-specific and health-related QoL outcome measures, and economic evaluations to inform policymakers regarding cost-effectiveness. This RCT on focal therapy versus usual care is urgently needed to enable focal therapy to overgrow the experimental status, provide the evidence needed for guidelines, and make this available for selected patients who benefit from this strategy. Because of its promising results in other countries, focal therapy is increasingly requested by patients, but due to the lack of high-quality evidence, it is not reimbursed yet. This has been designated by both the PCa patient support group and physicians as a failure of both the market and the funding agencies.
At present, all devices that are used in the proposed study are CE approved and no safety issues were reported in IDEAL stage 1 and 2a studies. For high-risk PCa, local radical therapy has been found to significantly improve oncological endpoints. However, for low- and intermediate-risk localized PCa, the different recommended options by guidelines (radical prostatectomy (RP), radiotherapy (RT), or active surveillance (AS)) have similar short- to medium-term oncological outcomes in randomized studies. A PROZIB database search and a KWF report showed that about 65% of the intermediate-risk patients that are eligible for focal therapy currently undergo either RP or RT. Furthermore, brachytherapy is only used to a limited extent (7%) in intermediate-risk patients in the Netherlands, and since it is not offered as a treatment option in the participating hospitals in this proposal, the investigators do not include this option in our study.
Active surveillance is mainly used for low-risk patients rather than for the intermediate-risk patients the investigators are aiming for in this study. Our systematic review concluded that more high-quality evidence is required before focal therapy can become available as a standard treatment. The majority of focal therapy studies were prospective development IDEAL stage 2a studies (feasibility studies), showing the limited adverse impact on functional outcomes and favorable oncological outcomes. Overall, focal therapy studies reported a median of 95% pad-free at 1-year and 85% of the patients had no clinically significant cancer in the treated area, respectively. High-quality multi-center comparative clinical trials, however, appear to be lacking. The appropriate management of patients with recurrent PCa following focal therapy has been an ongoing point of discussion. Marra et al. showed that evidence from assessments of salvage treatments after focal therapy failure is low and is derived from four retrospective salvage series. Available salvage options after focal therapy include RP and RT. Overall oncological outcomes are acceptable, although biochemical recurrence is slightly higher compared to primary PCa treatment, probably because of the higher aggressiveness of recurrent/persistent PCa. Functional outcomes and complications are not markedly worse compared to primary treatment. Salvage RP and salvage RT, therefore, seem feasible treatment options with acceptable oncological control and functional outcomes. Thus, re-treatment with salvage radiotherapy or salvage surgery remains a clinical option after focal therapy failure. Experience from other countries and our qualitative research on this topic taught us that many patients will consciously opt for an initial focal therapy to maintain their quality of life and because they can be treated later when deemed necessary with the other options.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 45 Years 至 —(Adult, Older Adult)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Gleason score of 7 (3 + 4 or 4 + 3; ISUP grade 2/3)
- •PSA level of ≤ 20 ng/ml
- •Clinical stage ≤ T2b disease
- •Life expectancy of ≥ 10 years
- •Men with a prostate size ≤ 5 cm in sagittal length and ≤ 6 cm in axial length
- •Fit, eligible, and normally destined for radical surgery or radiotherapy
- •No concomitant cancer
- •No previous treatment of their prostate
- •An understanding of the Dutch language sufficient to receive written and verbal information about the trial, its consent process and the study questionnaires
排除标准
- •Unfit for general anesthesia or radical surgery
- •Low volume low-risk disease (≤4mm Gleason score of ≤ 6 / ISUP grade 1)
- •High-risk disease (Gleason score of ≥ 8 / ISUP grade >3)
- •Clinical T3 disease (extracapsular PCa)
- •Men who have received previous active therapy for PCa.
- •Men with evidence of extraprostatic disease.
- •Men with an inability to tolerate a transrectal ultrasound.
- •Cardiac pacemaker
- •Metal implants/stents in the urethra or prostate.
- •Prostatic calcification/cysts that interfere with effective delivery of TULSA/HIFU based on MRCT.
- •Men with renal impairment and a glomerular filtration rate (GFR) of < 30 ml/minute/1.73 m
- •Unable to give consent to participate in the trial, as judged by the attending clinicians
研究组 & 干预措施
Focal therapy
Patients in this group will receive focal therapy, i.e. TULSA, IRE or Hifu.
干预措施: Focal therapy (Procedure)
Usual care
Patients in this group will receive usual care for prostate cancer, i.e. radical prostatectomy or radiotherapy
干预措施: Usual care (Procedure)
结局指标
主要结局
Quality of life (superiority) measured with Functional Assessment of Cancer Therapy-Prostate questionnaire
时间窗: 12 months
Compare quality of life between the two arms measured with the FACT-P questionnaire. FACT-P scores of the subscales vary between 0-24 and 0-28, the total score is between 0-156. The higher the score, the better.
Oncological effectiveness (non-inferiority) defined as treatment failure
时间窗: 36 months
i.e. pathologically proven recurrent disease and/or the indication for retreatment with salvage treatment (RP, RT or systemic treatment or RT) in the focal therapy group and as biochemical recurrence and/or salvage treatment in the usual care group
次要结局
- Health-related quality of life using the International Consultation on Incontinence Questionnaire(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Health-related quality of life using the 5-dimension health-related quality of life from the uroQol group(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Health-related quality of life using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire for prostate cancer(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Disease progression(60 months)
- Disease specific mortality(60 months)
- Metastasis-free survival(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Health-related quality of life using the Sexual Health Inventory for Men International Index of Erectile Function-5 questionnaire(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Cost-effectiveness will be measured using the iMTA Medical Consumption Questionnaire(60 months)
- Health-related quality of life regarding urinary symptoms using the International Prostate Symptom Score questionnaire(at baseline, 3, 6, 12, 24, 36, 48 and 60 months)
- Hospital care stay(Immediately after procedure)
- Pathology results after biopsy and/or radical prostatectomy(60 months)
- All-cause mortality(60 months)
- Operating time(Immediately after the procedure)
- Adverse events(60 months)
- Cost-effectiveness will be measured using the IMTA Productivity Cost Questionnaire(60 months)
