A Pilot Study of Dose dE-eScalaTion IN prostATe radIOtherapy usiNg the MRL (DESTINATION)

Netherlands Cancer Institute (NKI)

Status

Active, not recruiting

Conditions

Prostate Cancer

Treatments

Radiation: De-escalated radiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06284304

N22DES

Details and patient eligibility

About

Trial design: A single centre phase II non-randomised study

Trial population: Men with intermediate risk localised prostate cancer

Recruitment target: 20 patients in total

Trial objectives:

Primary To develop a 5 fraction de-escalated dose SBRT protocol capable of reducing side effects
Secondary
- To assess levels of acute GU and GI toxicity (CTCAE)
- To assess levels of late GU and GI toxicity (CTCAE)
- To assess late sexual quality of life (expanded EPIC, IIEF-5)
- To assess biochemical relapse-free survival at 2 years

Trial treatment: All radiotherapy will be delivered on the MR-linac. Intraprostatic dose will be varied according to risk of local recurrence, based on mpMRI, PSA and histology. The whole prostate will receive 30 Gy in 5 fractions and the GTV plus intra-prostatic margin will receive an isotoxic 45 Gy prescription.

Full description

Primary endpoint: Technical feasibility of treating prostate cancer with toxicity- minimising radiotherapy on an MR-linac

Secondary endpoint:

Physician reported GU and gastrointestinal (GI) toxicity (CTCAE grade) at baseline and the end of treatment then at 4 weeks and 3 months post-treatment.
Late toxicity (CTCAE v5.0) at 1 and 2 years post-treatment
Patient-reported outcome measures (PROMs) from the EPIC-26, IPSS, and IIEF-5 questionnaires. Patients will be asked to complete PROMs at 4 weeks, 3 and 6 months, 1 and 2 years post treatment.
PSA control and kinetics at 2 years post-treatment

Quality of life: EPIC-26 QoL will be measured at baseline, then at 4 weeks and 3, 6, 12 and 24 months from end of treatment. IIEF-5 will be completed at baseline and months 6, 12 and 24. IPSS will be measured at all time points.

Follow-up: Patients will be assessed at 6, 12 and 24 months and then as per standard of care.

Enrollment

20 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Men aged ≥18 years
Histological confirmation of prostate adenocarcinoma requiring radical radiotherapy
Gleason score 3+3, 3+4 or 4+3 (Grade groups 1, 2 or 3)
MRI stage T2 or less (as staged by AJCC TNM 2018)
MRI-visible tumour(s) of PIRADS v2 grade 3 or higher on T2 and diffusion-weighted imaging and/or dynamic contrast-enhanced imaging with concordant pathology
Dominant lesion <50% of prostate on any axial slice and <50% total prostate volume
PSA <20 ng/ml prior to starting ADT
Patients can be concurrently treated with androgen deprivation therapy if this would be standard of care. LHRH analogues or Bicalutamide are permitted. ADT is not mandatory where this would usually be omitted.
WHO Performance status 0-2
Ability of the participant understand and the willingness to sign a written informed consent form.
Ability/willingness to comply with the patient reported outcome questionnaires schedule throughout the study.

Exclusion criteria

Contraindications to MRI (e.g. pacemaker, potentially mobile metal implant, claustrophobia)
IPSS 19 or higher
High grade disease (GG3) occult to MRI-defined lesion
Post-void residual >100 mls, where known
Prostate volume >90cc
Comorbidities which predispose to significant toxicity (e.g. inflammatory bowel disease) or preclude long term follow up
Unilateral or bilateral total hip replacement, or other pelvic metalwork which causes artefact on diffusion-weighted imaging
Previous pelvic radiotherapy
Patients needing >6 months of ADT due to disease parameters.
Previous invasive malignancy within the last 2 years excluding basal or squamous cell carcinomas of the skin, low risk non-muscle invasive bladder cancer (assuming cystoscopic follow up now negative) or small renal masses on surveillance