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Effect of Probiotics Supplementation on the Side Effects of Radiation Therapy Among Colorectal Cancer Patients

Primary Purpose

Colorectal Cancer

Status
Withdrawn
Phase
Phase 2
Locations
Jordan
Study Type
Interventional
Intervention
Probiotic Formula Capsule
Control
Sponsored by
King Hussein Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring Colorectal cancer, Radiotherapy, immune system, Inflammatory markers, Life quality

Eligibility Criteria

35 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Men or women,
  2. Aged from 35- 65 years with histologically proven CRC and
  3. Histologically proven CRC with stage I, II, III
  4. Will exposed newly to radiotherapy with the absence of any psychological, sociological or geographical condition that potentially affects the compliance with the study protocol and follow-up schedule.

Exclusion Criteria:

  1. Active infection treated by antibiotic therapy or recent infection or recent antibiotic use;
  2. Severe cardiovascular and cerebrovascular diseases that could not tolerate radical surgery;
  3. Recent use of probiotics, prebiotics, or synbiotic;
  4. Evidence of immunodeficiency;
  5. Cancer stage IV
  6. Pregnancy,
  7. Recent/concurrent admission to ER
  8. Co-existence of other malignant neoplasms, no other type of cancer in the past 5 years, any serious concomitant systemic disorders or diseases incompatible with the study.

Sites / Locations

  • King Hussein Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Probiotic Formula Capsule

Control

Arm Description

In this intervention arm the patients will receive oral viable capsules of probiotic contain (1*10 10 colony forming unit (CFU)/g) of lactobacillus (Lactobacillus rhamnosus , Lactobacillus acidophilus , Lactobacillus reuteri, Lactobacillus paracasei, Lactobacillus casei, Lactobacillus gasseri, Lactobacillus plantarum) and bifidobacteria (Bifidobacterium lactis, Bifidobacterium breve, Bifidobacterium bifidum, Bifidobacterium longum, Bifidobacterium infantis) species three times a per day

In this intervention arm, the control arm will receive normal treatment without any probiotic

Outcomes

Primary Outcome Measures

The level of Immunoglobulin (Ig) A
The level of Immunoglobulin (Ig) A in g/L at both baseline and end line of intervention
The level of Immunoglobulin (Ig) G
The level of Immunoglobulin (Ig) G in g/L at both baseline and end line of intervention
The level of Immunoglobulin (Ig) M
The level of Immunoglobulin (Ig) M in g/L at both baseline and end line of intervention
The Level of Interleukin (IL)-6
The Level of Interleukin (IL)-6 in pg/ml at both baseline and end line of intervention
The Level of Interleukin (IL)-1
The Level of Interleukin (IL)-1 in pg/ml at both baseline and end line of intervention
The Level of Interleukin (IL)-10
The Level of Interleukin (IL)-10 in pg/ml at both baseline and end line of intervention
The Level of Tumor Necrosis Factor (TNF)-α
The Level of TNF-α in pg/ml at both baseline and end line of intervention
The Level of C-reactive protein (CRP)
The Level of CRP in mg/ml at both baseline and end line of intervention

Secondary Outcome Measures

Quality of Life of patients
The average score of the general quality of life (QoL) subscales assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaires (EORTC-QLQ) which use five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea and vomiting) range from"Not at A Quite Very" to "Very Much " , and a single global health status/QoL scale range from one (very poor) to 7(Excellent) . In addition, the questionnaire contains five symptom scales that are commonly reported by cancer patients (dyspnea, loss of appetite, insomnia, constipation, and diarrhea) and the perceived financial impact of the disease scale that range from"Not at A Quite Very" to "Very Much ".
The gastrointestinal toxicity
Number and percent of participants with treatment-related adverse events as assessed by NCI Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE) change from baseline in the occurrences and grad of Adverse Events on grading scale at 5 Weeks

Full Information

First Posted
November 11, 2018
Last Updated
March 13, 2023
Sponsor
King Hussein Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT03742596
Brief Title
Effect of Probiotics Supplementation on the Side Effects of Radiation Therapy Among Colorectal Cancer Patients
Official Title
Effect of Probiotics Supplementation on the Side Effects of Radiation Therapy on the Immune System Among Colorectal Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Withdrawn
Why Stopped
This study was closed without recruitment
Study Start Date
November 7, 2018 (Actual)
Primary Completion Date
September 30, 2022 (Anticipated)
Study Completion Date
December 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
King Hussein Cancer Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Colorectal cancer (CRC) is one of the most common types of cancer worldwide in general and in Jordan in specific. The studies that investigate the role of Probiotics supplementation in improving the inflammatory response, gastrointestinal toxicity and life quality of patients with colorectal cancer during radiotherapy are limited. So, this study aimed to study the effect of probiotics on the response of inflammatory markers, gastrointestinal toxicity, and quality of life in patients with colorectal cancer during radiation therapy. An interventional double-blind randomized clinical trial (RCT) design will be used in this study. Forty patients will be recruited and assigned either to receive 3 times a day probiotic supplement or to be control with no intervention. The demographic data, anthropometric measurements, Cancer Quality of Life Questionnaire and blood samples will be collected at baseline and at end of radiation therapy. Interleukin-6, interleukin-1,interleukin-10 IL-10, C-reactive protein, tumor necrosis factor-alpha and complete blood count (CBC) will be measured. The results will approve or disapprove the beneficial effect of using probiotics as adjuvant therapy for CRC patients and other types of cancer to reduce the side effects of radiotherapy and raise body weight as well as improving their quality of life.
Detailed Description
To meet the objectives of the study, a control group will be included in parallel with the treatment group in this trail. Forty patients (aged 35-65 years) who recently diagnosed with CRC will be recruited conveniently from the radiation oncology clinic at the King Hussein Cancer Center (KHCC), Amman, Jordan. Patients who meet the inclusion criteria and agree to participate and to take the drug will be allocated to the probiotic supplementation group, while patients who agree to participate but not to receive the drug will be allocated to the control group. The duration of the intervention will be 5 weeks, from the day of radiation until the end of treatment. For the participants, the King Hussein Cancer Center (KHCC) hospital setting will be utilized for data collection. The patients will be recruited over 12 months and all patients will be asked to sign a written informed consent before enrollment. The patients that will be assigned to the probiotics group (n=20), to receive 3 times a day probiotic supplement. The duration of the intervention (administration of probiotics) will start 10-14 days before radiotherapy and continue over the 5 weeks duration of treatment under the supervision of the treating physician and end with the end of radiation therapy. The blood sample will be collected at baseline and at the end of radiation therapy and 10-14 days after radiation therapy. The demographic data of each subject will be collected such as; gender, age, body mass index (BMI), tumor location, malignant tumors stage, tumor differentiation, educational level, occupation, family history, smoking, dietary and physical activity. At baseline and end line of the radiation therapy, a Cancer Quality of Life Questionnaire C30 (QLQ-C30) will be collected and blood sample tests will be withdrawn and the following biochemical variables will be measured: immunoglobulin G, immunoglobulin M, immunoglobulin A, interleukin-6 (IL-6), C-reactive protein (CRP), interleukin-1(IL-1), interleukin-10(IL-10), interleukin-12 (IL-12), Tumor necrosis factor-alpha (TNF-α) and complete blood count (CBC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colorectal cancer, Radiotherapy, immune system, Inflammatory markers, Life quality

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotic Formula Capsule
Arm Type
Experimental
Arm Description
In this intervention arm the patients will receive oral viable capsules of probiotic contain (1*10 10 colony forming unit (CFU)/g) of lactobacillus (Lactobacillus rhamnosus , Lactobacillus acidophilus , Lactobacillus reuteri, Lactobacillus paracasei, Lactobacillus casei, Lactobacillus gasseri, Lactobacillus plantarum) and bifidobacteria (Bifidobacterium lactis, Bifidobacterium breve, Bifidobacterium bifidum, Bifidobacterium longum, Bifidobacterium infantis) species three times a per day
Arm Title
Control
Arm Type
Other
Arm Description
In this intervention arm, the control arm will receive normal treatment without any probiotic
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic Formula Capsule
Other Intervention Name(s)
Treatment
Intervention Description
The Probiotic will be coded in a specific label by a researcher. The patient will receive 2 bottles of the drug every 2 weeks and will be followed weekly for 7 weeks.
Intervention Type
Drug
Intervention Name(s)
Control
Intervention Description
The Placebos will be coded in a specific label by a researcher.
Primary Outcome Measure Information:
Title
The level of Immunoglobulin (Ig) A
Description
The level of Immunoglobulin (Ig) A in g/L at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The level of Immunoglobulin (Ig) G
Description
The level of Immunoglobulin (Ig) G in g/L at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The level of Immunoglobulin (Ig) M
Description
The level of Immunoglobulin (Ig) M in g/L at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The Level of Interleukin (IL)-6
Description
The Level of Interleukin (IL)-6 in pg/ml at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The Level of Interleukin (IL)-1
Description
The Level of Interleukin (IL)-1 in pg/ml at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The Level of Interleukin (IL)-10
Description
The Level of Interleukin (IL)-10 in pg/ml at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The Level of Tumor Necrosis Factor (TNF)-α
Description
The Level of TNF-α in pg/ml at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 year
Title
The Level of C-reactive protein (CRP)
Description
The Level of CRP in mg/ml at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Secondary Outcome Measure Information:
Title
Quality of Life of patients
Description
The average score of the general quality of life (QoL) subscales assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaires (EORTC-QLQ) which use five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea and vomiting) range from"Not at A Quite Very" to "Very Much " , and a single global health status/QoL scale range from one (very poor) to 7(Excellent) . In addition, the questionnaire contains five symptom scales that are commonly reported by cancer patients (dyspnea, loss of appetite, insomnia, constipation, and diarrhea) and the perceived financial impact of the disease scale that range from"Not at A Quite Very" to "Very Much ".
Time Frame
Through study completion, an average of 1 year
Title
The gastrointestinal toxicity
Description
Number and percent of participants with treatment-related adverse events as assessed by NCI Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE) change from baseline in the occurrences and grad of Adverse Events on grading scale at 5 Weeks
Time Frame
Through study completion, an average of 1 year
Other Pre-specified Outcome Measures:
Title
The level of White blood cell count (WBC)
Description
he level of WBC as cells/ul at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of red blood cell count (RBC)
Description
The level of RBC as cells/ul at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The mean corpuscular volume (MCV)
Description
The MCV in fl at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The mean corpuscular hemoglobin (MCH)
Description
The MCH in pg at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The mean corpuscular hemoglobin concentration (MCHC)
Description
The MCH in g/dl at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The Platelet count
Description
The Platelet count as cells/ ul at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The of Hemoglobin
Description
The Hemoglobin in g/dl at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The mean platelet volume (MPV)
Description
The MPV in fl at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of lymphocytes
Description
The number of lymphocytes cells at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of Monocytes
Description
The number of Monocytes cells at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of eosinophils
Description
The number of eosinophils cells at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of basophils
Description
The number of basophils cells at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea
Title
The level of neutrophils
Description
The number of neutrophils cells at both baseline and end line of intervention
Time Frame
Through study completion, an average of 1 yea

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men or women, Aged from 35- 65 years with histologically proven CRC and Histologically proven CRC with stage I, II, III Will exposed newly to radiotherapy with the absence of any psychological, sociological or geographical condition that potentially affects the compliance with the study protocol and follow-up schedule. Exclusion Criteria: Active infection treated by antibiotic therapy or recent infection or recent antibiotic use; Severe cardiovascular and cerebrovascular diseases that could not tolerate radical surgery; Recent use of probiotics, prebiotics, or synbiotic; Evidence of immunodeficiency; Cancer stage IV Pregnancy, Recent/concurrent admission to ER Co-existence of other malignant neoplasms, no other type of cancer in the past 5 years, any serious concomitant systemic disorders or diseases incompatible with the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fawzi Abuhijla, MD,MSc
Organizational Affiliation
King Hussein Cancer Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lana M Agraib, PhD
Organizational Affiliation
University of Jordan
Official's Role
Principal Investigator
Facility Information:
Facility Name
King Hussein Cancer Center
City
Amman
Country
Jordan

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The center (KHCC) where the study conducted emphasis of maintaining privacy and confidentiality of the participants' data
Citations:
PubMed Identifier
19640788
Citation
Abayomi J, Kirwan J, Hackett A. The prevalence of chronic radiation enteritis following radiotherapy for cervical or endometrial cancer and its impact on quality of life. Eur J Oncol Nurs. 2009 Sep;13(4):262-7. doi: 10.1016/j.ejon.2009.02.007. Epub 2009 Jul 28.
Results Reference
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PubMed Identifier
24607309
Citation
Abdollahi H. Probiotic-based protection of normal tissues during radiotherapy. Nutrition. 2014 Apr;30(4):495-6. doi: 10.1016/j.nut.2013.09.006. No abstract available.
Results Reference
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Citation
Abdollahi, H., Shiri, I., Atashzar, M., Sarebani, M., Moloudi, K., and Samadian, H. (2015), Radiation protection and secondary cancer prevention using biological radioprotectors in radiotherapy. International Journal of Cancer Therapy and Oncology, 3(3).
Results Reference
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PubMed Identifier
27048903
Citation
Ambalam P, Raman M, Purama RK, Doble M. Probiotics, prebiotics and colorectal cancer prevention. Best Pract Res Clin Gastroenterol. 2016 Feb;30(1):119-31. doi: 10.1016/j.bpg.2016.02.009. Epub 2016 Feb 19.
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PubMed Identifier
17881902
Citation
Bowen JM, Stringer AM, Gibson RJ, Yeoh AS, Hannam S, Keefe DM. VSL#3 probiotic treatment reduces chemotherapy-induced diarrhea and weight loss. Cancer Biol Ther. 2007 Sep;6(9):1449-54. doi: 10.4161/cbt.6.9.4622. Epub 2007 Jun 23.
Results Reference
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PubMed Identifier
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Citation
Ciernikova S, Mego M, Semanova M, Wachsmannova L, Adamcikova Z, Stevurkova V, Drgona L, Zajac V. Probiotic Survey in Cancer Patients Treated in the Outpatient Department in a Comprehensive Cancer Center. Integr Cancer Ther. 2017 Jun;16(2):188-195. doi: 10.1177/1534735416643828. Epub 2016 May 5.
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PubMed Identifier
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Ciorba MA, Hallemeier CL, Stenson WF, Parikh PJ. Probiotics to prevent gastrointestinal toxicity from cancer therapy: an interpretive review and call to action. Curr Opin Support Palliat Care. 2015 Jun;9(2):157-62. doi: 10.1097/SPC.0000000000000134.
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PubMed Identifier
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Citation
Dai C, Zheng CQ, Meng FJ, Zhou Z, Sang LX, Jiang M. VSL#3 probiotics exerts the anti-inflammatory activity via PI3k/Akt and NF-kappaB pathway in rat model of DSS-induced colitis. Mol Cell Biochem. 2013 Feb;374(1-2):1-11. doi: 10.1007/s11010-012-1488-3. Epub 2012 Oct 23.
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Dasari S, Kathera C, Janardhan A, Praveen Kumar A, Viswanath B. Surfacing role of probiotics in cancer prophylaxis and therapy: A systematic review. Clin Nutr. 2017 Dec;36(6):1465-1472. doi: 10.1016/j.clnu.2016.11.017. Epub 2016 Nov 24.
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Effect of Probiotics Supplementation on the Side Effects of Radiation Therapy Among Colorectal Cancer Patients

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