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A Novel Oral Synbiotic Formula in Reducing Adenoma Recurrence and Colorectal Neoplasia-related Bacterial Gene Markers

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Enrolling

Conditions

Colorectal Adenoma
Colorectal Neoplasms
Colorectal Cancer

Treatments

Other: SMT04 formula
Other: Active placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05592886
2022.360

Details and patient eligibility

About

This double blinded randomized controlled trial aims to assess the efficacy of a novel oral synbiotic formula (SMT04) in reducing adenoma recurrence and colorectal neoplasia-related bacterial gene markers after endoscopic resection of colorectal advanced neoplasia.

Full description

Recent evidence has demonstrated the association between altered gut microbiome environment and the progression of colorectal cancer (CRC) from its precancerous lesions. Some pathogenic species of bacteria, including Fusobacterium nucleatum, Escherichia Coli and Bacteroides fragilis, have shown to be significantly enriched in CRC patients. This gut dysbiosis process also brings with its diagnostic potential for recurrent adenomas. Previous study found a panel of bacterial gene markers, including "m3" from Lachnoclostridium, F. nucleatum (Fn), Bacteroides clarus (Bc) and Clostridium hathewayi (Ch) could be used in detecting adenoma recurrence after polypectomy in a retrospective study. In addition, these microbial biomarkers may have prognostic potential and provide an option as therapeutic target.

Probiotics, including the genera Bifidobacterium and Lactobacillus, have shown to be able to inhibit tumorigenesis and progression of CRC in animal studies. Prebiotics are non-digestible dietary ingredients with protective effects against cancer by selectively stimulating the growth and activity of beneficial colonic microbiota. The combination of probiotics and prebiotics, known as synbiotic, may be more efficient in preventing CRC than either one alone.

The investigators' unpublished data showed that the new probiotic formula containing Bifidobacterium strains has a negative correlation with CRC-related bacterial gene markers. Subjects treated with SMT04 showed significantly higher levels of the individual Bifidobacterium species at week 2 to week 5 compared with baseline levels. There was a significant decrease in the bacterial gene markers (Fn, m3 and 4Bac CRC risk score) from week 2 to week 12 compared with baseline levels in the SMT04 group but not in the control group. The synbiotic formula (SMT04) is the combination of probiotic formula and several heat-resistant prebiotics. It remains unclear that whether this synbiotic formula can produce a sustained effect in reduction of adenoma recurrence and colorectal neoplasia related bacterial gene markers in long-term.

Enrollment

246 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Subjects have advanced colorectal neoplasia requiring endoscopic resection (endoscopic mucosal resection, endoscopic submucosal dissection, etc.);
  • They have received high quality colonoscopies before or during endoscopic resection (defined as a full colonoscopy with successful caecal intubation, and a Boston Bowel Preparation Scale ≧2 in each colonic segment);
  • Aged 18-90 years old;
  • Written informed consent obtained

Exclusion criteria

  • Known residual colorectal neoplasia not removed (except hyperplastic polyps);
  • Contraindications to endoscopic resection due to deep submucosal invasion;
  • Prior surgical resection of colon;
  • Personal history of hereditary polyposis syndrome or inflammatory bowel disease;
  • Known pregnancy or lactation;
  • Immunocompromised status (e.g. on immunosuppressants (except 5-aminosalicylic acid or short term use of corticosteroids <4 weeks), on chemotherapy, bone marrow or solid organ transplant, human immunodeficiency virus, congenital immune deficiency);
  • Advanced comorbid conditions (defined as American Society of Anesthesiologists grade 4 or above);
  • Refusal to undergo surveillance colonoscopy.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

246 participants in 2 patient groups, including a placebo group

Intervention arm
Experimental group
Description:
Receive SMT04 formula
Treatment:
Other: SMT04 formula
Placebo arm
Placebo Comparator group
Description:
Receive active placebo
Treatment:
Other: Active placebo

Trial contacts and locations

2

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Central trial contact

Louis Lau

Data sourced from clinicaltrials.gov

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