Addition of Focal Boost to Primary Radiotherapy for Prostate Cancer in 12 or 20 Fractions

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

1016 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-15

Study Completion Date

2040-10-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Every year, about 700 Danish men get radiotherapy for prostate cancer with a high-risk of later progression. The risk of relapse is about 40 % after 5 - 8 years, so we need better treatment for these patients in Denmark and globally. The aim is to reduce later cancer spreading, need of hormone treatments and prostate cancer death.

DAPROCA 10 tests two possible improvements:

If a higher dose (boost) to intra-prostatic tumor lesions improves cure rates. If the radiotherapy can be given with 12 treatment fractions instead of 20 without increased side-effects.

In this randomised trial half the participants get a boost and the other half don't. Half the patients get 12 treatments, the other half 20.

To answer these questions we must include1016 participants. The trial is feasible because the technological advances in imaging and radiotherapy enables us to define the tumors in the prostate and to deliver the boost to the tumors with high precision, without increased dose to the surrounding organs.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Salvage HDR for Locally Recurrent Prostate Cancer

NCT04231006

Prostate Cancer

RECRUITING NA

Trial of Ultrahypofractionated Focal Salvage Radiotherapy for Isolated Prostate Bed Recurrence After Radical Prostatectomy

NCT05746806

Recurrent Prostate Cancer

ACTIVE_NOT_RECRUITING NA

Feasibility Study of a Dose Increase by a Boost of Curietherapy in Pulse Dose Rate (PDR) Associated With the Extern Radiotherapy in Prostate Cancer

NCT01039038

Prostate Cancer With Intermediate Risk

TERMINATED PHASE2

Study of Hypo-fractionated Proton Radiation for Low Risk Prostate Cancer

NCT01230866

Prostate Cancer

ACTIVE_NOT_RECRUITING PHASE3

Study of Radiation Therapy in Combination With Darolutamide + Degarelix in Intermediate Risk Prostate Cancer

NCT04176081

Prostate Cancer

NOT_YET_RECRUITING PHASE2

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Addition of focal boost to primary radiotherapy for prostate cancer in 12 or 20 fractions: A large DAPROCA randomised trial.

Purpose

The DAPROCA multidisciplinary group is planning a large trial to answer two pertinent questions of how to improve radiotherapy for high - and intermediate risk prostate cancer:

1. Will increasing dose to intra-prostatic cancer lesions improve outcomes with respect to prostate cancer without increasing toxicity?
2. Is it possible to shorten the treatment without increased toxicity?

The success of both increased dose to intra-prostatic cancer lesions and shortening of treatment, which means treatment with fewer treatment fractions with higher dose per fraction, is most likely dependent on high quality, high precision radiotherapy (RT) planning and delivery. A French randomised trial in prostate cancer demonstrated improved rectal toxicity scores (p=\<0.03) and biochemical control with image guidance, and the MIRAGE randomised trial demonstrated improvements with smaller margins and more precise delivery (1-3). Many European clinics, including the Danish RT-clinics are able to provide high quality RT to all patients as per national consensus guidelines and in this study, we aim to further develop and implement this high quality opportunities in order to deliver hypofractionated RT and to boost the dose to intraprostatic lesions in all participating centers.

Background Prostate cancer (PCa) is the second most common malignancy in men worldwide, and the most common cancer in Denmark. The incidence of PCa has been increasing in most coun-tries and varies between countries. In Denmark, the incidence is now 124/100.000 men per year, and the median age for men diagnosed with PCa is 72 years. In the public, PCa is con-sidered to have a good prognosis, but the fact is that the mortality is high with 1323 Danish men annually dying from PCa, exceeding the age-standardised breast cancer mortality (nordcan,https://nordcan.iarc.fr/en). The prognosis and the treatment of PCa depends on pa-tient factors, as well as the histology grade, the prostate specific antigen (PSA) level, and the extent of disease.

This trial focuses on the group of patients with intermediate and high risk PCa, who have a risk of relapse of 25 - 60% and a risk of getting metastatic disease of up to 20 % after 5 - 8 years.

Large, randomised trials have shown improved oncological outcomes, including overall sur-vival, and disease specific survival for RT combined with androgen deprivation therapy (ADT) compared to ADT only. In addition, large, randomised trials have shown a benefit with RT and ADT compared to RT only. In 2023 in Denmark, 463 high risk patients and 144 intermediate risk patients received definitive RT with 36+ fractions. The RT is delivered with intensity mod-ulated RT (IMRT) and with prostate implanted fiducial markers for image guidance (IGRT). The RT clinics follow national guidelines securing the quality of treatment.

Endocrine treatment Endocrine treatment in combination with definitive RT has been standard of care for many years. The addition of 6-36 months of ADT has been shown to significantly improve overall survival (OS) in high risk and selected intermediate risk patients. Recent results revealed that two years of abiraterone acetate plus 3 years of ADT further improved the OS in patients with lymph node involvement or in high risk patients patients with two of three risk factors (\>=cT3a, PSA ≧ 40, ISUP\>=4).

Elective pelvic lymph node radiotherapy Elective pelvic lymph node radiotherapy (PLNRT) is offered in Denmark as a standard of care to PCa patients referred to definitive RT with either pelvic lymph node metastases or patients with a risk of lymph node metastases above 5- 7%. Risk of lymph node metastases can be estimated using different nomograms e.g. the Roach Formula, the Briganti nomogram 2012, Briganti nomogram 2019, and the Briganti nomogram 2023. Risk estimation can be based on imaging with PSMA PET/CT, mpMRI, PSA level, ISUP grade, T stage, tumour size, and the percentage of systematic prostate core biopsies with cancer. The benefit of elective pelvic lymph node irradiation is dependent on the risk of lymph node involvement, the higher the risk of lymph node involvement the more likely the patient is to benefit. Trials indicate im-provement of outcome and pelvic nodes can be included safely with contemporary radiother-apy techniques with tolerable risks of gastro-intestinal toxicity and edema.

Increased dose to intra-prostatic cancer lesions A strategy to improve outcome is dose escalation to the cancer lesions in the prostate. The FLAME randomised trial (NCT01168479) demonstrated improved biochemical control, re-duced local failure (LF) and reduced regional + distant metastatic failure. Toxicity is the limit-ing factor, and the boost dose was strictly limited depending on organ at risk exposure (OAR) in the FLAME trial. A dose response analysis for biochemical control indicated that patients with higher achieved boost doses experienced better tumour control. At the same time, the data suggested reduced toxicity as a result of further consideration of radiation dose to OARs and improved urethral sparing in particular. The question is therefore whether the addition of a focal boost can be established as standard of care.

A study larger than FLAME is needed in order to confirm effectiveness with freedom from distant metastases (FFDM) as an improved primary endpoint, compared to biochemical con-trol which was used as primary endpoint in FLAME. However, while endpoints based on bio-chemical relapse free survival are not surrogate for overall survival in localised prostate can-cer, FFDM is now shown to be a valid surrogate endpoint for OS in trials of localised prostate cancer. Biochemical control is used as a secondary endpoint in the current study to confirm the FLAME results and study heterogeneity of treatment effects as detailed in the statistics section.

Shortening of treatment duration In recent years, different approaches have been taken to decrease the number of fractions of prostate RT. These schedules reduce the number of hospital visits for patient convenience and cost-efficiency improvements. The large randomised CHHiP trial has shown good results with a 20-fraction schedule, albeit excluding the very high-risk patients. One study compared 78 Gy in 39 fractions with 60 Gy in 20 fractions and shortening treatment was not inferior re-garding biochemical disease-free survival or toxicity. One phase III study in locally advanced disease showed more acute, but similar long-term gastro-intestinal toxicity with the same tu-mour control in patients treated with 64.6 Gy / 19 fractions than with 78 Gy/39 fractions. Early results of a high-risk patient only trial including 329 patients were published in May 2023, showing that moderate hypo-fractionation RT is well-tolerated, similar to standard fractiona-tion RT at 2 years. These findings are in agreement with a large meta-analysis concerning moderate hypofractionation for high-risk PCa patients who also received pelvic lymph node irradiation, with the conclusion that moderate hypofractionation could be considered an alter-native to standard fractionated RT.

Ultra-hypofractionation trials show promising results but are currently not conclusive enough to be considered standard of care. The second research question is therefore to ultimately investigate if a shorter treatment of patients with intermediate and high-risk PCa, including treatment to pelvic lymph nodes, can be introduced.

In our study, the dose to elective lymph nodes is either 45 Gy in 20 fractions (2.25 Gy per fraction) or 37 Gy in 12 fractions (3.08 Gy per fraction). The table below provides an over-view of selected studies in which fractionations between 2 - 5 Gy have been used for pelvic lymph node radiotherapy.

Imaging During the recent two decades, imaging procedures have shown to improve accuracy of staging in prostate cancer. T stage is still strictly based on digital rectal examination, however multiparametric MRI is now standard staging procedure in order to predict extra prostatic ex-tension, seminal vesicle involvement, T-staging and to guide biopsies. Recently, PET using radioactive ligands binding to the prostate-specific membrane antigen (PSMA) combined with CT (PSMA-PET/CT) has shown higher accuracy for N and M staging and PSMA-PET/CT is now according to international guidelines the recommended staging procedure N and M stage even though the prognosis and ideal management of patients diagnosed as metastatic by these more sensitive tests is unknown.

MRI has been shown to improve accuracy of prostate delineation and to correlate with histol-ogy and definition of intra-prostatic lesions with MRI has shown a high accuracy. Recently, the combination of PSMA-PET and MRI has demonstrated even higher accuracy.

Based on the randomised trials showing benefit of radiotherapy with combined hormone- and radiotherapy compared to hormone therapy only, 3 months pre-irradiation castration is stand-ard for high-risk patients in many institutions. Studies have addressed weakening MRI signals and PSMA PET-uptake after castration. However, there is not enough data to guide us to the optimal imaging to define intra-prostatic lesions in patients who are treated with a combination of medical castration and radiotherapy. Currently this topic is being investigated in a phase 2 study (Danish Ethical Committee 2303938), conducted by the research group to prepare for the present study.

Additional improvements in delivery, such as MRI based image guidance, improved CT based image guidance, or adaption of the daily dose plan to the anatomy of the day etc. may improve outcomes further. If participating centers implement follow local adaptive strategies for adaptation due to anatomical changes, the center must document the procedures.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Prostate Cancer Patients Undergoing External Radiation and Seed Implantation High Risk Localised Prostate Carcinoma Locally Advanced Prostate Cancer Unfavourable Intermediate Risk Prostate Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

The trial is an open, randomised, 2 x 2 factorial design, randomising between:

1. Boost or no boost to intra-prostatic tumour lesions.
2. 20 fractions in 4 weeks versus 12 fractions in 2½ weeks.

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

20 treatment fractions no boost

Prostate and seminal vesicles: 60 Gy/ 20 fractions. Pelvic: 45 Gy /20 fractions.

Group Type ACTIVE_COMPARATOR