Effect of a Reduced Dose Enzalutamide in Frail (m)CRPC Patients on Cognitive Side Effects

NCT ID: NCT03927391

Last Updated: 2024-06-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 57 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-05-30
• Study Completion Date: 2024-01-08

Brief Summary

Prostate cancer is the most commonly diagnosed cancer among men in Western countries. When the disease recurs as castration-resistant prostate cancer (CRPC) it is associated with a median overall survival of approximately 2 years with significant decrement in quality of life due to additional cancer-specific and treatment-induced morbidity. Palliative agents currently used in the CRPC setting include the 2nd generation hormonal agents abiraterone acetate and enzalutamide but also radium-223, docetaxel and cabazitaxel. Choices for treatment strategies are based on multiple factors such as age, co-morbidity and drug toxicity profile. The side effect profile of enzalutamide is associated with central nervous system (CNS side effects) such as fatigue and depression. The mechanism for these side effects is not yet fully understood, but it was shown in rodent studies that enzalutamide and its active metabolite penetrate into the CNS. This might cause the CNS side effects that were later seen in the phase 1 study where fatigue was found to be a dose-dependent adverse event. After dose reductions the symptoms resolved. This was also found in a retrospective study of Japanese metastatic CRPC (mCRPC) patients (n=345) in which the side effects malaise and nausea decreased remarkably after dose reduction. However, no exposure-response relation was observed in the study of Gibbons et al. Additionally, based on the data of the phase 1 trial of enzalutamide it can be suggested that a minimum trough concentration of 5.0 mg/L could be considered as a target for exposure to enzalutamide. In particular, frail (m)CRPC patients are more prone to develop CNS side effects on enzalutamide. The investigator's hypothesis is that dose reduction to 75% (120mg) can be safely done to treat (m)CRPC in these patients with preserving optimal efficacy and less CNS side effects.

Conditions

Prostatic Neoplasms, Castration-Resistant

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

reference (normal) dose

Normal dose of enzalutamide (160mg once daily)

Group Type: ACTIVE_COMPARATOR

Enzalutamide

Intervention Type: DRUG

enzalutamide treatment

test (reduced) dose

Reduced dose of enzalutamide (120mg once daily)

Group Type: EXPERIMENTAL

Enzalutamide

Intervention Type: DRUG

enzalutamide treatment

Interventions

Enzalutamide

enzalutamide treatment

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Frailᵃ male patients with prostate cancer who will start treatment with enzalutamide within label
• Age at least 18 years
• Patient who are able and willing to give written informed consent prior to screening
• Patients from whom it is possible to collect blood samples
• Patients who are willing to answer the questionnaires and test
• Life expectancy of > 6 months
• Capable of understanding and answering Dutch tests and questionnaires, as determined by the investigator

ᵃ Frail is defined as:

• a score on the comprehensive G8 assessment with cut-off ≤14 points and
• score ≥grade 1 for Central Nervous Disorders according to the Common Toxicity Criteria Adverse Event (CTCAE) criteria, of one of the following: Fatigue, Concentration impairment, cognitive disturbance, amnesia, depressed level of consciousness, memory impairment, hypersomnia.

Exclusion Criteria

• change in dose of opioids/sedatives/benzodiazepines during last 2 weeks before study)
• Use of psychostimulants such as methylphenidate within 1 week of start of study
• Diagnosed with medical conditions that affect cognition: Dementia, Alzheimer disease, Parkinson's disease, psychiatric disorders that affect cognition other than depression or anxiety complaints related to the disease
• Active infection or other comorbidities that may contribute to REDOSE, February 2019 Page 7 of 53 fatigue or cognition change within 4 weeks of study entry
• Clinical relevant anaemia
• MoCa score <20
• Hypersensitivity to the active substance or to any of the excipients.

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Radboud University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CWZ

Nijmegen, , Netherlands

Radboudumc

Nijmegen, , Netherlands

Franciscus Gasthuis en Vlietland hospital

Rotterdam, , Netherlands

Countries

Netherlands

References

Boerrigter E, Overbeek JK, Benoist GE, Somford DM, Hamberg P, Tol J, Scholtes B, Willemsen AECAB, Buffart LM, Kessels RPC, Mehra N, van Oort IM, van Erp NP. A Prospective Randomised Trial to Determine the Effect of a Reduced Versus Standard Dose of Enzalutamide on Side Effects in Frail Patients with Prostate Cancer. Eur Urol Oncol. 2024 Dec;7(6):1376-1383. doi: 10.1016/j.euo.2024.02.009. Epub 2024 Mar 13.

Reference Type: RESULT

PMID: 38485614 (View on PubMed)

Other Identifiers

REDOSE

Identifier Type: -

Identifier Source: org_study_id