Chronic Radiation Induced Bowel Toxicity Study

Официальное название

Chronic Radiation Induced Bowel Toxicity Study (CRIBS)

Обзор

In the UK over 22,000 people undergo pelvic radiotherapy treatment per year, for several types of cancers including prostate cancer. The investigators want to investigate whether there are any differences in the bacteria in the bowel in patients with prostate cancer and whether these change during treatment. The aim of this study is to analyse the bacteria from the stool of patients undergoing radiotherapy for prostate cancer. The investigators will also look for any changes in the urine, blood and using rectal swabs that might be a surrogate for what is happening in the gut at the same time. They will collect food frequency/ food diary information for each patient alongside health questionnaires. The investigators aim to recruit approximately 50 patients diagnosed with prostate cancer due to undergo radiotherapy over a two year period. Patients will be recruited across 2 sites (Rosemere Cancer Centre, Lancashire Teaching Hospitals Trust and The Christie NHS Foundation Trust).

Подробное описание

This is a prospective, translational study which aims to investigate the radiation induced immunological changes in the bowel mucosa, blood and urine, and the role of the microbiota in acute and late bowel toxicity.

The investigators aim to recruit 50 patients newly diagnosed with (histologically confirmed) localised, intermediate to high-risk prostate cancer (T2b -T4a N0 M0), who are due to undergo standard of care radical radiotherapy (Intensity modulated radiotherapy (IMRT)) (60Gy in 20# with curative intent) 4-week regimen.

Eligible patients who have consented to the study will provide the following samples at baseline (prior to the start of radiotherapy), weekly during radiotherapy for 4 weeks, 6-8 weeks and 12 from the start of radiotherapy, and at 6-month and 12-month follow-up appointments:

1. stool sample 2. blood sample (40mls) delegated nurse or research nurse. 3. mid-stream urine sample 4. optional rectal swab 5. quality of life health questionnaire

4-day diet diaries will be completed by the patients in the 4 days prior to providing their baseline stool samples and at follow-up appointments (6-8 weeks, 6 months, 12 months).

Вмешательства

• Процедура Procedure - blood, urine and stool sample collection
  Samples will be collected (blood, urine, stool and optional rectal swab) at baseline (prior to the start of radiotherapy), weekly during radiotherapy for 4 weeks, 6-8 weeks and 12 weeks from start of radiotherapy, and at 6-month and 12-month follow-up appointments

Первичные конечные точки

• Feasibility of obtaining longitudinal blood, urine and stool samples [Срок оценки: From enrolment until 12 months post treatment]

Критерии участия

Критерии включения

• Male, aged ≥ 18; no upper age limit and able to give informed consent.
• Newly diagnosed patients with, histologically confirmed, localised, intermediate to high-risk prostate cancer (T2b -T4a N0 M0).
• Patients to be treated with prostate radical radiotherapy IMRT (60Gy in 20# with curative intent) 4-week regimen.
• Performance status - ECOG 0-2.

Критерии исключения

• Had received systemic antibiotics (intravenous, intramuscular, or oral) within 2 months before enrolment.
• Had received cytotoxic or immunosuppressive therapies within 6 months of enrolment, including chemotherapy or immunotherapy.
• Had consumed large doses of commercial probiotics (greater or equal to 108 CFU per day) within 12 months of enrolment (such as Actimint®, CranProBio®, ImmunoProBio®, among others).
• Patients with diagnosed inflammatory bowel disease or coeliac disease
• Patients with previous colorectal cancer
• Patients who have undergone colectomy (total or subtotal)
• Patients with a history of diverticulitis (uncomplicated diverticular disease permitted)

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

Великобритания · 2 центра

• Christie NHS Foundation Trust — Manchester
• Lancashire Teaching Hospitals NHS Foundation Trust — Preston

Идентификаторы

NCT: NCT06640959 · CFTsp225

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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