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HRQOL in Prostate Cancer Patients Treated With Radiotherapy

Health-Related Quality of Life in Prostate Cancer Patients Treated With Radiotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05645237
Acronym
PRORAD
Enrollment
600
Registered
2022-12-09
Start date
2019-04-08
Completion date
2030-06-01
Last updated
2025-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

prostate cancer, radiotherapy, hypofractionation, health-related quality of life

Brief summary

The study primarily aims at evaluating health-related quality of life after radiotherapy for prostate cancer, using modern hypofractionated radiotherapy schedules. Study design is a prospective observational cohort study. All patients give written informed consent and fill out online validated questionnaires before, during, and after radiotherapy (yearly) up to 5 years post-treatment.

Detailed description

Rationale: Patient-Reported Outcomes (PROs), such as health-related quality of life (HRQL), have achieved an important role in the evaluation of benefits and harms after cancer treatment, including radiotherapy for prostate cancer (PCa). In the past year, clinical radiotherapy protocols at the Erasmus MC have been changed for external beam radiotherapy (EBRT) as well as for brachytherapy (BT). In order to evaluate the current, changed, clinical practice, we will conduct a prospective cohort study, with the main purpose to assess HRQL for the current treatment options at the Erasmus MC. Objective: To establish HRQL (start treatment - 5 years after treatment) in a prospective cohort of ≈600 patients with localized PCa treated with radiotherapy within in the period ≈ 1/3/2019 - 1/12/2023. Main objective: to establish changes in HRQL levels (with respect to baseline) up to 5 year post-treatment, within each radiotherapy modality for prostate cancer patients, i.e. EBRT 60 Gy in 20 fractions, EBRT 42.7 Gy in 7 fractions, CyberKnife (stereotactic EBRT) 38 Gy in 4 fractions, BT 27 Gy in 2 fractions, postoperative EBRT (PORT) 72 Gy in 36 fractions, EBRT for LN+: 70 Gy (prostate)/52 Gy (lymph nodes) in 28 fractions. Study design: Prospective observational cohort study. Study population: Patients with prostate cancer T1c-T4 referred for radiotherapy at the Erasmus MC as a primary treatment with curative intent or as first line adjuvant treatment after a prostatectomy. Intervention: All interventions are according to applicable standard clinical procedures & protocols for localized prostate cancer of the Radiotherapy department. Main study parameters/endpoints: HRQL scores of the EPIC (urinary domain, bowel domain), and the IIEF-5 (sexual function) score. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There are no additional risks or benefits for patients that participate in the study. The additional burden is to fill out questionnaires at regular intervals. Study patient recruitment period was from April 2019 to May 2025, enrolling about 695 eligible patients, mainly treated with UHF 7x6.1 Gy (n=240), MHF 20x3/3.1 Gy (n=210), PORT (n=85), and brachytherapy (n=65).

Interventions

RADIATIONradiotherapy

Radiotherapy is delivered with linear accelerators or cyberknife (external beam radiotherapy), or local irradiation with high dose rate brachytherapy (brachytherapy)

Sponsors

Dutch Cancer Society
CollaboratorOTHER
Erasmus Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Clinically T1c-T4, N0 (or N+ in case of EBRT-LN+), M0 prostate cancer patient referred for radiotherapy. * Willing and capable to fill out Dutch questionnaires on health-related items at a computer (online questionnaires). * Signed written Informed Consent.

Exclusion criteria

* Previously radiation treatment in the pelvic region, for any reason. * Diagnosed with other tumor in the past 12 months or known with tumor progression of another tumor. * Postoperative radiotherapy with dose levels \< 72 Gy.

Design outcomes

Primary

MeasureTime frameDescription
Sexual functioning score on IIEF-5 questionnaireYear 1- Year 4Sexual functioning score on International Index of Erectile Function (IIEF-5) questionnaire: 1 to 25 scale, higher scores imply better function
EPIC questionnaire score on bowel domainYear 1 - Year 4Expanded Prostate Cancer Index Composite (EPIC) Bowel Domain score: a 0 to 100 scale with higher scores representing better HRQOL.
EPIC questionnaire score on urinary domainYear 1 - Year 4Expanded Prostate Cancer Index Composite (EPIC) Urinary Domain score: a 0 to 100 scale with higher scores representing better HRQOL.

Secondary

MeasureTime frameDescription
Late moderate to severe urinary incontinenceYear 1 - Year 4Score of 'more than once a week or daily leaking of urine' on the Expanded Prostate Cancer Index Composite (EPIC) Urinary Domain.
Late moderate to severe urinary frequency during the nightYear 1 - Year 4Score of 'moderate/big problem for waking up to urinate' on the Expanded Prostate Cancer Index Composite (EPIC) Urinary Domain.
Acute rectal bleeding, on symptom checklist (patient-reported)During radiotherapy - 3 months after radiotherapyRectal bleeding is scored on a symptom checklist on a Likert scale (bother: none, little, quite, a lot) (patient-reported), higher score means worse symptoms. This symptom checklist was locally developed and used in previous trials.
Acute mucous discharge, on symptom checklist (patient-reported)During radiotherapy - 3 months after radiotherapyMucous discharge is scored on a symptom checklist on a Likert scale (bother: none, little, quite, a lot) (patient-reported), higher score means worse symptoms. This symptom checklist was locally developed and used in previous trials.
Late moderate to severe incontinence for stoolsYear 1 - Year 4Score of 'more than once a week or daily uncontrolled leakage of stools/feces' on the Expanded Prostate Cancer Index Composite (EPIC) Bowel Domain.
Late frequent bowel movementsYear 1 - Year 4Score of 'more than five' daily bowel movements on the Expanded Prostate Cancer Index Composite (EPIC) Bowel Domain.
Late erectile dysfunctionYear 1- Year 4Score of 'very low/low confidence to get and keep an erection' on the International Index of Erectile Function (IIEF-5) questionnaire.

Other

MeasureTime frameDescription
Acute moderate to severe rectal discomfortDuring radiotherapy - 3 months after radiotherapyScore of 'quite/a lot' for the symptom 'pain with stools' and/or 'cramping urge',
General health score on EQ-5D-5L questionnaireYear 1- Year 4General health score on EuroQoL 5-dimensions, 5-levels (EQ-5D-5L) questionnaire: total score between -1 - +1,higher score indicates better quality of life.
Late gastrointestinal painYear 1 - Year 4Score of 'moderate/big problem for abdominal/pelvic/rectal pain' on the Expanded Prostate Cancer Index Composite (EPIC) Bowel Domain.
Late watery bowel movementsYear 1 - Year 4Score of 'moderate/big problem for watery bowel movements' on the Expanded Prostate Cancer Index Composite (EPIC) Bowel Domain.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026