Cancer of the Prostate Treated With Focal Implantation of a RadioactivE Source (CAPFIRE)

Herlev Hospital

Status

Invitation-only

Conditions

Prostate Cancer

Treatments

Radiation: Focal Brachytherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06080113

H-22046020

Details and patient eligibility

About

The purpose is to assess and describe the oncological and functional outcomes following the introduction of curative targeted focal brachytherapy of prostate cancer in Denmark.

Men with a single MRI-identifiable prostate cancer index-tumour who fulfil inclusion criteria and are candidates for curative treatment. Eligible men will undergo curative intended targeted focal brachytherapy for treatment of histologically confirmed prostate cancer.

The intervention will include Low- (LDR) or High (HDR) dose rate targeted focal brachytherapy of prostate cancer. Collection of data on safety, morbidity, side effects and quality of life. Collection of clinical data on treatment efficacy, progression, and mortality.

All patients will have a follow up of 10-years for oncological outcome, 5-years for acute- and late toxicity-, and 2-years for functional outcomes, respectively. The follow up will include clinical data, MRI, confirmatory biopsies, and questionnaires at specific fixed time points pre-and post-operatively after 1-3 days, 4-weeks, 3-, 6--, 9-, 12-, 18-, and 24-months followed by every 6 months up to 5-yr and then every year up to 10-yr follow-up.

Anticipated number of patients is 50 and regular analysis and reporting will be performed continuously. The first short-term analysis will be after 18-months of follow-up after confirmatory MRI and biopsies, and the final reporting will be after 10-years follow-up in 2035.

Enrollment

50 estimated patients

Sex

Male

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 40-80; Performance status 0-1; >10 yr. life expectancy
Candidate for curative intended treatment
PSA <20 ng/mL
Clinical stage T1c or T2a
Prostate anatomy suitable for focal brachytherapy
MRI identified index tumour (PI-RADS 3-5) with PCa confirmed on biopsy
A single index tumour focus with Gleason score 6 (>10 mm maximum cancer-core length [MCCL]), Gleason score 3+4 (any MCCL) or Gleason core 4+3 (<10 mm MCCL)
Systematic biopsies (≥10-12 cores) with no or low volume Gleason score 6 (3+3) PCa only
No severe urinary obstructive symptoms (e.g., urinary retention needing indwelling catheter)
Fit to undergo all procedures in the protocol
Included subjects should be able to participate in the planned follow-up (either on-site visits or telephone consultation accepted at specific time-points).
Included subjects should be able to read and understand the study details, and provide written informed consent to participate

Exclusion criteria

If any of the following criteria is present, the subject cannot participate in the study:

Not a candidate for curative intended treatment (e.g., other active malignancy except for non-melanoma skin-cancer, life-expectancy <10 years, severe comorbidities etc.)
Prior surgical or radiation treatment of PCa; Prior transurethral-resection (TUR-P) is not an exclusion criterion.
Evidence/suspicion of extra prostatic extension on MRI
Tumour focus >50% of one prostate half on MRI corresponding to stage >T2a
Briganti 2018 score ≥7%
PCa with intraductal carcinoma, cribriform pattern, or small cell component
Any anatomical or clinical conditional not suitable for brachytherapy (e.g., imperforate anus, prostatitis, inflammatory bowel disease, severe calcifications etc.)
Any contraindication for prostate MRI (e.g., claustrophobia, pacemaker, estimated glomerular filtration rate ≤30 mL/min/1.73m2)
Reduction in MRI image quality that interferes with diagnosis caused by e.g., hip replacement surgery or other metal implants in the pelvic area.
Any medical condition precluding procedures
Any medication that may alter prostate morphology or alter MRI appearance (e.g., 5-alpha reductase inhibitors, prior androgen deprivation therapy [ADT])
Subjects who are unwilling or unable to adhere to the study requirements (including treatment, required assessments and follow-up).