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

Official title

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

Overview

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.

Detailed description

Abiraterone and enzalutamide (AA/ENZ) are drugs which are being used to treat metastatic prostate cancer. These drugs are a form of additional hormonal therapy and have been used for many years. For most patients, these drugs work well and the prostate cancer stays under control for several months to years. In all patients, there will be a moment when the prostate cancer doesn't respond anymore to the treatment. This is called resistance. This leads to increasement of PSA, tumor growth on the CT-scan and/or bone scan or decline of condition. The investigators want to establish if it is possible to delay the development of resistance by using the drugs differently. It is now recommended to use AA/ENZ daily until the prostate cancer doesn't respond anymore to the treatment. During treatment, all cancer cells sensitive to treatment will die and all cells resistant for treatment will survive. Based on evolutionary principles, this might not be a wise strategy. The groups of resistant cancer cells will prevail and will grow faster and faster. This will lead to increasement of PSA, tumor growth on the CT-scan and/or bone scan or decline of condition. The investigators want to establish if it is better to not take the treatment drugs daily, but to pause the treatment on regular basis. The theory of the investigators is that, due to just in time pausing the treatment, a part of the treatment sensitive cells will remain alive. These treatment sensitive cancer cells will compete with the treatment resistant cells for limited space and nutrients. In this way, the treatment sensitive cancer cells prevent the accelerating growth of the treatment resistant cancer cells. Due to this phenomenon, the investigator hypothesis is the prostate cancer will respond longer to treatment. It will take longer until a new treatment is necessary or until a patients develops complaints. When the treatment is paused, patients might experience less side effects. It is easy to establish whether the prostate cancer responds to treatment by measuring PSA.

Interventions

• Other Patient-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 (dea
• Drug Abiraterone acetate
  Use of abiraterone or enzalutamide
• Drug Enzalutamide
  Use of abiraterone or enzalutamide

Primary outcome measures

• Time to treatment failure [Time frame: Time from randomization until death by any cause, or until criteria for treatment failure are met. PSA progression and clinical progression will be measured every 4 weeks, radiographic progression every 12 weeks, both up to 3 years after randomization.]

Secondary outcome measures (8)

• Time to PSA progression while on treatment [Time frame: Time from randomization until an increase of PSA of >25% and >2 ng/mL persisting while a patient is on consecutive treatment for at least 8 weeks or death. PSA will be measured every 4 weeks until 3 years after randomization.]
• Radiographic progression-free survival while on study treatment [Time frame: Time from randomization to death or the first occurrence of radiographic progression while a subject received treatment between the imaging tests. Bone scan and CT-scan will be measured every 12 weeks until 3 years after randomization.]
• Overall survival [Time frame: Time from randomization to the date of death due to any cause. Measured every 4 weeks up to 3 years after randomizaton and after end of treatment visit every 6 months until 2 years after end of treatment visit.]
• Time to first skeletal-related event [Time frame: Time from randomization to first skeletal-related event or death. Bone scan and CT-scan will be measured every 12 weeks up to 3 years after randomization.]
• Health Related Quality of Life - FACT-P [Time frame: FACT-P questionnaire will be obtained every 12 weeks up to 3 years after randomization]
• Health Related Quality of Life - EQ-5D-5L [Time frame: EQ-5D-5L questionnaire will be obtained every 12 weeks up to 3 years after randomization]
• Health Related Quality of Life - Pain [Time frame: Brief Pain Inventory questionnaire will be obtained every 12 weeks up to 3 years after randomization]
• Adverse events [Time frame: Adverse events will be measured every 12 weeks, up to 3 years after randomization.]

Eligibility criteria

Inclusion criteria

• Willing and able to provide informed consent;
• Aged 18 or older;
• Histologically or cytologically confirmed adenocarcinoma of the prostate;
• Ongoing androgen deprivation therapy with a GnRH analogue or bilateral orchiectomy (i.e. surgical or medical castration with testosterone at screening ≤1.7 nmol/L (<0.5 ng/mL)); patients who have not had a bilateral orchiectomy, must have a plan to maintain effective GnRH-analogue therapy for the duration of the trial;
• Presence of metastatic disease on WBBS and/or CT-scan;
• Progressive disease at study entry defined as per PCWG3 as one or more of the following criteria that occurred while the patient was on ADT:

• PSA progression defined by a minimum of 2 rising PSA levels with an interval of ≥1 week between each determination. Patients who received an anti-androgen must have progression after withdrawal (≥4 weeks since last flutamide or ≥6 weeks since last bicalutamide or nilutamide); OR
• Radiographic PD on bone scintigraphy and/or CT-scan;
• A PSA concentration of ≥2 ng/mL.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
• Controlled symptoms (opioids for cancer related pain stable for >4 weeks, no need for urgent radiotherapy for symptomatic lesions);
• Estimated life expectancy of ≥12 months;
• Patient has archival prostate cancer tissue available and which he consents to share or is willing to undergo a new tumour biopsy;
• Adequate organ function: absolute neutrophil count > 1,500/μL (> 1.5\*109/L); platelet count > 100,000/μL (> 100\*109/L), haemoglobin > 90 g/L; total bilirubin < 1.5 times ULN, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 3 times ULN; creatinine < 175 μmol/L; albumin > 30 g/L;
• Any other therapies for CRPC (excluding denosumab and bisphosphonates) have to be discontinued 3 weeks prior to study randomisation;
• Able to swallow the study drug and comply with study requirements.

Exclusion criteria

• Life-threatening or serious medical or psychiatric illness that could, in investigator's opinion, potentially interfere with participation in this study;
• Diagnosis or treatment for another systemic malignancy within 2 years before the first dose of study drugs. Potential participants with non-melanoma skin cancer, non-muscle invasive bladder cancer, or carcinoma in situ of any type are allowed if they have undergone complete resection;
• Known or suspected brain metastasis or leptomeningeal disease;
• Small-cell or neuroendocrine differentiation of prostate cancer;
• Radiation therapy for treatment of the primary tumour within 3 weeks of screening visit;
• Radiation or radionuclide therapy for treatment of metastasis within 3 weeks of screening visit, excluding radiation to reduce pain symptoms;
• History of uncontrolled seizures (if patient and investigator wish to choose treatment with enzalutamide)
• Unstable symptomatic ischemic heart disease, ongoing arrhythmias or New York Heart Association (NYHA) Class III or IV heart failure;
• Known HIV infection, active chronic hepatitis B or C;
• Known gastrointestinal (GI) disease that could interfere with GI absorption/tolerance of study drugs;
• Prior treatments with CYP17 inhibitors (e.g. ketoconazole) or novel androgen receptor inhibitors (e.g. abiraterone, apalutamide, darolutamide or enzalutamide). Bicalutamide and nilutamide should be stopped >6 weeks before screening visit. Prior treatment with docetaxel in the mHSPC setting is allowed.
• Any condition or reason that, in the opinion of the Investigator, interferes with the ability of the patient to participate in the trial, which places the patient at undue risk, or complicates the interpretation of safety data.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

Australia · 12 centers

• Border Medical Oncology Research Unit / The Border Cancer Hospital — Albury
• Chris O'Brien Lifehouse — Camperdown
• St George Hospital — Kogarah
• Calvary Mater Newcastle — Newcastle
• Genesis Care North Shore — St Leonards
• Sydney Adventist Hospital — Wahroonga
• Sunshine Coast University Hospital — Birtinya
• Mater Hospital Brisbane — South Brisbane
• … and 4 more centers

Netherlands · 7 centers

• Radboud Univeristy Medical Centre — Nijmegen
• Spaarne Gasthuis — Hoofddorp
• Isala Ziekenhuis — Zwolle
• Groene Hart Ziekenhuis — Gouda
• Leids Universitair Medisch Centrum — Leiden
• Meander Medical Centre — Amersfoort
• University Medical Center Groningen — Groningen

Identifiers

NCT: NCT05393791 · 79835 · ANZUP 2101

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗