RecruitingPhase 2NCT05393791

Phase II Randomised Controlled Trial of Patient-specific Adaptive vs. Continuous Abiraterone or eNZalutamide in mCRPC

ANZadapt: Phase II Randomised Controlled Trial of Patient-specific Adaptive Versus Continuous Abiraterone or eNZalutamide in Metastatic Castration-resistant Prostate Cancer


Sponsor

Leiden University Medical Center

Enrollment

168 participants

Start Date

Nov 10, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Hormone tablets, abiraterone (Zytiga®) and enzalutamide (Xtandi®) are approved to treat advanced prostate cancer. However, even if these drugs are helpful, their effectiveness usually diminishes over time. Small pilot studies have indicated that using hormone tablets sparingly, for just long enough to control the cancer, followed by a break in treatment and restarting them later, seems to improve how long hormone tablets can control the cancer. This study aims to find out if this pause/restart strategy is better than taking hormone tablets every day continuously. The study will include 168 people with metastatic castrate resistant prostate cancer in the Netherlands and Australia. Patients will be randomly 1:1 assigned between the control group and the experimental group. In the control group, patients will take the treatment with AA/ENZ every day until the prostate cancer doesn't respond anymore to the treatment. In the experimental group, patients will start with daily AA/ENZ until the PSA has declined for \>50%. The treatment will then be paused and monthly PSA measurements will be performed. The treatment will be re-initiated when the PSA has increased to the level of before starting treatment. The treatment will be continued daily until the PSA has again dropped for \>50%. This pause/restart cycle will be repeated until the prostate cancer doesn't respond anymore to the treatment.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adapting radiation therapy to each individual patient's unique anatomy — using multiple MRI scans taken during treatment to adjust the radiation field in real time — can improve outcomes for people with prostate cancer that has returned and spread to pelvic lymph nodes. **You may be eligible if...** - You are 18 or older - You have confirmed prostate cancer by biopsy (adenocarcinoma) - Your cancer has returned and is located in the pelvic lymph nodes - You are currently receiving hormone therapy (androgen deprivation therapy) - You are willing and able to undergo multiple MRI scans during treatment **You may NOT be eligible if...** - You have a serious life-threatening medical or psychiatric illness that could interfere with treatment - You have been diagnosed with another cancer within the past 5 years - You have previously had pelvic radiation that would make additional treatment unsafe - You are unable to lie still for MRI or radiation sessions Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERPatient-specific adaptive therapy

Patients will start taking abiraterone or enzalutamide (AA/ENZ) daily. PSA will be measured every month as well as radiological evaluation by CT-scan and bone scan. Treatment will be continued until PSA has dropped \>50%. The treatment will then be paused. Once the PSA has risen again above the pretreatment baseline, treatment will be re-initiated. AA/ENZ will be stopped again after the PSA declines \>50% from the baseline. This will be continued until criteria for treatment failure are met (death by any cause or at least 2 out of 3 of the following events while on treatment: radiographic progression on CT-scan and/or bone scan, PSA progression or clinical progression).

DRUGAbiraterone acetate

Use of abiraterone or enzalutamide

DRUGEnzalutamide

Use of abiraterone or enzalutamide


Locations(19)

Border Medical Oncology Research Unit / The Border Cancer Hospital

Albury, New South Wales, Australia

Chris O'Brien Lifehouse

Camperdown, New South Wales, Australia

St George Hospital

Kogarah, New South Wales, Australia

Calvary Mater Newcastle

Newcastle, New South Wales, Australia

Genesis Care North Shore

St Leonards, New South Wales, Australia

Sydney Adventist Hospital

Wahroonga, New South Wales, Australia

Sunshine Coast University Hospital

Birtinya, Queensland, Australia

Mater Hospital Brisbane

South Brisbane, Queensland, Australia

Royal Adelaide Hospital

Adelaide, South Australia, Australia

ICON Cancer Centre

Adelaide, South Australia, Australia

Eastern Health Box Hill

Box Hill, Victoria, Australia

Fiona Stanly Hospital

Murdoch, Western Australia, Australia

Radboud Univeristy Medical Centre

Nijmegen, Gelderland, Netherlands

Spaarne Gasthuis

Hoofddorp, North Holland, Netherlands

Isala Ziekenhuis

Zwolle, Overijssel, Netherlands

Groene Hart Ziekenhuis

Gouda, South Holland, Netherlands

Leids Universitair Medisch Centrum

Leiden, South Holland, Netherlands

Meander Medical Centre

Amersfoort, Utrecht, Netherlands

University Medical Center Groningen

Groningen, Netherlands

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