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PROstate CAncer Radiotherapy - Bowel Quality of Life (PROCAR-BQ) (PROCAR-BQ)

Primary Purpose

Prostate Cancer, Radiotherapy Side Effect, Bowel Dysfunction

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Bowel symptoms & QoL assessment
Sponsored by
Jules Bordet Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring Prostate Cancer, Radiotherapy Side Effect, Radiation Toxicity, Bowel Dysfunction, Pelvic Radiation Disease, Diarrhea, Radiation Proctitis, Radiation enteritis, Quality of Life, Malnutrition, Sarcopenia, Diet, Physical activity

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: Men with PCa which are candidate for pelvic radiotherapy (RT) with or without previous surgery, with or without concomitant hormonotherapy (HT), Performance status (PS) 0-2 (all patient able to undergo RT treatment), of all age, elderly included. Exclusion Criteria: Previous RT to the pelvis Diagnosed Inflammatory Bowel Disease (IBD), celiac disease Severe GI symptoms before the beginning of RT (Grade > 2 according to CTCAE grading system) Obvious cognitive impairment, Inability to understand French/English and no contact person able to accompany and translate.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    Bowel symptoms & QoL assessment

    Arm Description

    This single arm study represent a group a patient with prostate cancer who are candidate for pelvic radiotherapy. Patient reported outcomes on bowel toxicity and overall quality of life will be systematically assessed right before and after RT. Various potential predictive factors will be analysed.

    Outcomes

    Primary Outcome Measures

    Mean Delta of EORTC Proctitis Module (PRT20) score
    Mean Delta between the end and the beginning of RT (4 weeks) in PRT20 score (Min 18, Max 72, higher scores mean worse outcome)

    Secondary Outcome Measures

    Mean Delta of EORTC Quality of Life Questionnaire (QLQ-C30) score
    Mean Delta between the end and the beginning of RT (4 weeks) in C30 score (For symptoms: Min 28, Max 112, higher scores mean worse outcome; For general status: Min 2, Max 14, higher scores mean better outcome)

    Full Information

    First Posted
    May 10, 2023
    Last Updated
    September 26, 2023
    Sponsor
    Jules Bordet Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05880446
    Brief Title
    PROstate CAncer Radiotherapy - Bowel Quality of Life (PROCAR-BQ)
    Acronym
    PROCAR-BQ
    Official Title
    PROstate CAncer Radiotherapy: Its Real Impact on Bowel Symptoms & Quality of Life Today, Measured by the EORTC QLQ C30 & Specific PRT20 Module.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    December 2023 (Anticipated)
    Study Completion Date
    January 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Jules Bordet Institute

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This is a prospective pilot study to evaluate the mean increase of bowel symptoms after pelvic radiotherapy (RT) in prostate cancer (PCa) patient using the validated & newly translated EORTC-QLQ PRT20 module.
    Detailed Description
    Questionnaires (QLQ-C30 and PRT20 modules) will be held to patients at the beginning and at the end of RT (4 weeks) to evaluate the mean increase of lower GI symptoms and decrease in overall QoL after pelvic RT. For exploratory objectives, GLIM (Global Leadership Initiative on Malnutrition) criteria for malnutrition diagnosis, a 24h recall and DQI-I calculation will be assessed by the PI before the start of RT. CT sim & dosimetry will be analyse by the PI before treatment to evaluation the body composition and the max and mean dose received by the bowel, the sigmoid and the rectum. A Polar watches will be loaned to the patient by the PI at the CT sim appointment to record patient's daily movement for two weeks (usual waiting time between CT and treatment) and recovered on the first day of treatment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Cancer, Radiotherapy Side Effect, Bowel Dysfunction, Quality of Life
    Keywords
    Prostate Cancer, Radiotherapy Side Effect, Radiation Toxicity, Bowel Dysfunction, Pelvic Radiation Disease, Diarrhea, Radiation Proctitis, Radiation enteritis, Quality of Life, Malnutrition, Sarcopenia, Diet, Physical activity

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Quality of life questionnaires and dietician advice before and at the end of treatment.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Bowel symptoms & QoL assessment
    Arm Type
    Other
    Arm Description
    This single arm study represent a group a patient with prostate cancer who are candidate for pelvic radiotherapy. Patient reported outcomes on bowel toxicity and overall quality of life will be systematically assessed right before and after RT. Various potential predictive factors will be analysed.
    Intervention Type
    Other
    Intervention Name(s)
    Bowel symptoms & QoL assessment
    Intervention Description
    QoL and bowel symptoms questionnaires will be held to patients, anthropomorphic measurement, handgrip test, physical activity level and usual diet quality of the patient will be assessed.
    Primary Outcome Measure Information:
    Title
    Mean Delta of EORTC Proctitis Module (PRT20) score
    Description
    Mean Delta between the end and the beginning of RT (4 weeks) in PRT20 score (Min 18, Max 72, higher scores mean worse outcome)
    Time Frame
    At study completion, an average of 4 months
    Secondary Outcome Measure Information:
    Title
    Mean Delta of EORTC Quality of Life Questionnaire (QLQ-C30) score
    Description
    Mean Delta between the end and the beginning of RT (4 weeks) in C30 score (For symptoms: Min 28, Max 112, higher scores mean worse outcome; For general status: Min 2, Max 14, higher scores mean better outcome)
    Time Frame
    At study completion, an average of 4 months
    Other Pre-specified Outcome Measures:
    Title
    Sarcopenia prevalence and its association with PRT20 and QLQ-C30 score Delta.
    Description
    Descriptive analysis of sarcopenia prevalence and its association with PRT20 and QLQ-C30 score Delta. Men with L3 skeletal muscle index < 52.4 cm2/m2 will be classified as having sarcopenia. Skeletal muscle cross-sectional area (SMA) in cm2 at the third lumbar vertebra will be measured on the CT simulation (2 weeks before RT start) then normalized for stature to report the L3 skeletal muscle index (SMI) in cm2/m2. Hand-grip strength will be assessed as supportive measure the same day.
    Time Frame
    At study completion, an average of 4 months
    Title
    Malnutrition prevalence and its association with PRT20 and QLQ-C30 score Delta.
    Description
    Descriptive analysis of GLIM (Global Leadership Initiative on Malnutrition) criteria for malnutrition diagnosis prevalence and its association with PRT20 and QLQ-C30 score Delta. One of the three positive phenotypic criteria will lead to positive diagnosis of malnutrition: >5 % weight loss within past 6 months (asked to patient during visit or compared to previous reports), BMI < 20-22 (weight and height will be combined to report BMI in kg/m^2), Reduces muscle mass by L3 skeletal muscle index < 52.4 cm2/m2 (skeletal muscle cross-sectional area in cm2 at the third lumbar vertebra will be measured by CT then normalized for stature to report the L3 skeletal muscle index in cm2/m2)
    Time Frame
    At study completion, an average of 4 months
    Title
    Max Dose on Bowel Bag, Sigmoid & Rectum and its association with PRT20 and QLQ-C30 score Delta.
    Description
    Descriptive analysis of Dmax in Gray (Gy) on Bowel Bag, Sigmoid & Rectum on RT plan dosimetry and its association with PRT20 and QLQ-C30 score Delta.
    Time Frame
    At study completion, an average of 4 months
    Title
    Mean Dose on Bowel Bag, Sigmoid & Rectum and its association with PRT20 and QLQ-C30 score Delta.
    Description
    Descriptive analysis of Dmean in Gray (Gy) on Bowel Bag, Sigmoid & Rectum on RT plan dosimetry and its association with PRT20 and QLQ-C30 score Delta.
    Time Frame
    At study completion, an average of 4 months
    Title
    Low Diet Quality Index prevalence and its association with PRT20 and QLQ-C30 Delta
    Description
    Descriptive analysis of Low Diet Quality Index (DQI-I) prevalence and its association with PRT20 and QLQ-C30 score Delta. DQI-I will be calculated from analysis of patient usual diet by the mean of a diet history and 24-h recall method before the start of RT and by it's conversion in nutritional values using composition tables. The continuous measure of the total DQI-I scores (Min 0, Max 100) of each patient will be categorized into quartiles (Very low, Low, Intermediate, High) and correlated to individual PRT20 and QLQ-C30 Delta in a descriptive manner.
    Time Frame
    At study completion, an average of 4 months
    Title
    Low Physical Activity Level prevalence and its association with PRT20 and QLQ-C30 Delta
    Description
    Descriptive analysis of Low Physical Activity Level (PAL) prevalence and its association with PRT20 and QLQ-C30 score Delta. Physical Activity Level will be recorded by the mean of Polar® Watches which will be loaned to the patient by the PI at the CT sim appointment for two weeks (usual waiting time between CT and treatment) and recovered on the first day of treatment
    Time Frame
    At study completion, an average of 4 months

    10. Eligibility

    Sex
    Male
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Men with PCa which are candidate for pelvic radiotherapy (RT) with or without previous surgery, with or without concomitant hormonotherapy (HT), Performance status (PS) 0-2 (all patient able to undergo RT treatment), of all age, elderly included. Exclusion Criteria: Previous RT to the pelvis Diagnosed Inflammatory Bowel Disease (IBD), celiac disease Severe GI symptoms before the beginning of RT (Grade > 2 according to CTCAE grading system) Obvious cognitive impairment, Inability to understand French/English and no contact person able to accompany and translate.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Pauline CI De Bruyn, MD
    Phone
    025413804
    Email
    pauline.debruyn@hubruxelles.be
    First Name & Middle Initial & Last Name or Official Title & Degree
    Clémence Al Wardi, PhD
    Phone
    025413981
    Email
    clemence.alwardi@hubruxelles.be

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    28640871
    Citation
    Delobel JB, Gnep K, Ospina JD, Beckendorf V, Chira C, Zhu J, Bossi A, Messai T, Acosta O, Castelli J, de Crevoisier R. Nomogram to predict rectal toxicity following prostate cancer radiotherapy. PLoS One. 2017 Jun 22;12(6):e0179845. doi: 10.1371/journal.pone.0179845. eCollection 2017.
    Results Reference
    background
    PubMed Identifier
    16814954
    Citation
    Heemsbergen WD, Peeters ST, Koper PC, Hoogeman MS, Lebesque JV. Acute and late gastrointestinal toxicity after radiotherapy in prostate cancer patients: consequential late damage. Int J Radiat Oncol Biol Phys. 2006 Sep 1;66(1):3-10. doi: 10.1016/j.ijrobp.2006.03.055. Epub 2006 Jul 11.
    Results Reference
    background
    PubMed Identifier
    24067488
    Citation
    Andreyev HJ, Benton BE, Lalji A, Norton C, Mohammed K, Gage H, Pennert K, Lindsay JO. Algorithm-based management of patients with gastrointestinal symptoms in patients after pelvic radiation treatment (ORBIT): a randomised controlled trial. Lancet. 2013 Dec 21;382(9910):2084-92. doi: 10.1016/S0140-6736(13)61648-7. Epub 2013 Sep 23.
    Results Reference
    background
    PubMed Identifier
    29360138
    Citation
    Lawrie TA, Green JT, Beresford M, Wedlake L, Burden S, Davidson SE, Lal S, Henson CC, Andreyev HJN. Interventions to reduce acute and late adverse gastrointestinal effects of pelvic radiotherapy for primary pelvic cancers. Cochrane Database Syst Rev. 2018 Jan 23;1(1):CD012529. doi: 10.1002/14651858.CD012529.pub2.
    Results Reference
    background
    PubMed Identifier
    28739383
    Citation
    Sini C, Noris Chiorda B, Gabriele P, Sanguineti G, Morlino S, Badenchini F, Cante D, Carillo V, Gaetano M, Giandini T, Landoni V, Maggio A, Perna L, Petrucci E, Sacco V, Valdagni R, Rancati T, Fiorino C, Cozzarini C. Patient-reported intestinal toxicity from whole pelvis intensity-modulated radiotherapy: First quantification of bowel dose-volume effects. Radiother Oncol. 2017 Aug;124(2):296-301. doi: 10.1016/j.radonc.2017.07.005. Epub 2017 Jul 21.
    Results Reference
    background
    PubMed Identifier
    30157890
    Citation
    Halkett GKB, Wigley CA, Aoun SM, Portaluri M, Tramacere F, Livi L, Detti B, Arcangeli S, Lund JA, Kristensen A, McFadden N, Grun A, Bydder S, Sackerer I, Greimel E, Spry N; EORTC Quality of Life Group. International validation of the EORTC QLQ-PRT20 module for assessment of quality of life symptoms relating to radiation proctitis: a phase IV study. Radiat Oncol. 2018 Aug 29;13(1):162. doi: 10.1186/s13014-018-1107-x.
    Results Reference
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    PROstate CAncer Radiotherapy - Bowel Quality of Life (PROCAR-BQ)

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