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Lynch SyndromeBioLynchNCT07838246

Liquid Biopsy Biomarkers for Endoscopic Surveillance in Lynch Syndrome

An observational study of Lynch Syndrome and Hereditary Nonpolyposis Colorectal Cancer, run by Fondazione IRCCS Istituto Nazionale dei Tumori, Milano at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Lynch syndrome (LS) is an autosomal dominant hereditary condition that markedly increases the risk of colorectal cancer (CRC) and other malignancies. Standard surveillance relies on colonoscopy every 1-2 years starting at age 20-25 years, an invasive and costly procedure that may become burdensome during lifelong… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Study procedures
How many people
109 participants
Where
1 siteItaly
Study dates
20 Jun 2023to 25 Jun 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with a confirmed pathogenic germline mismatch repair gene mutation (Lynch Syndrome) undergoing surveillance colonoscopy.

Who may be able to join

  • Patients with Lynch syndrome, defined as carriers of a pathogenic germline mutation in one of the mismatch repair genes (MLH1, MSH2, MSH6, PMS2, or EPCAM), able to sign informed consent.
  • Age ≥18 years.
  • Patients with Lynch syndrome without a cancer diagnosis in the 6 months preceding study entry (T0).

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Fondazione IRCCS Istituto Nazionale dei Tumori

    Milan, Italy, 20133

Other trials in Italy

About this study

Official title: Minimally Invasive Biomarkers to Improve Endoscopic Cancer Surveillance in Individuals With Lynch Syndrome: a Prospective Institutional Study

Lynch syndrome (LS) is an autosomal dominant hereditary condition that markedly increases the risk of colorectal cancer (CRC) and other malignancies. Standard surveillance relies on colonoscopy every 1-2 years starting at age 20-25 years, an invasive and costly procedure that may become burdensome during lifelong follow-up and may miss interval cancers. This prospective, single-institution, observational study aims to identify minimally invasive plasma, stool, and urine biomarkers that could improve the detection of early colorectal lesions in individuals with LS and help refine surveillance protocols.

Biomarker analyses include microsatellite instability (MSI) and MMR-related frameshift mutations in circulating tumor DNA, plasma and stool microRNA profiling, stool microbiome analysis, and exploratory urine cell-free DNA banking. Patients with genetically confirmed LS followed at Fondazione IRCCS Istituto Nazionale dei Tumori will be enrolled and followed for 24 months, undergoing surveillance colonoscopy at baseline, 12 months, and 24 months, with periodic venous blood sampling and stool, urine, and tissue collection according to protocol.

Read the detailed description

Rationale: Lynch syndrome is caused by germline pathogenic variants in one of the DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2, or EPCAM through MSH2 inactivation). Tumors arising in LS carriers characteristically exhibit microsatellite instability, which develops early during colorectal carcinogenesis, together with loss of expression of one or more MMR proteins on immunohistochemistry. MMR deficiency predisposes to frameshift mutations at coding mononucleotide repeats, and these mutations have recently been detected in the circulation of patients with MSI-high/MMR-deficient tumors.

In Italy, more than 50,000 new colorectal cancer cases are diagnosed each year, approximately 3-5% of which are associated with LS. Although LS is relatively uncommon, it is associated with a markedly increased lifetime risk of CRC, including an approximately 14-fold higher risk of developing CRC before the age of 50 compared with the general population, as well as an increased risk of metachronous tumors. Colonoscopic surveillance starting at 20-25 years of age and repeated every 1-2 years is currently the only established strategy to reduce CRC morbidity and mortality. However, colonoscopy is invasive, costly, and may become burdensome after years of lifelong surveillance, potentially affecting adherence. Moreover, interval cancers may develop between scheduled examinations.

Minimally invasive biomarkers capable of detecting early neoplastic changes could improve risk stratification, personalize surveillance intervals, and increase patient compliance. Circulating tumor-derived nucleic acids, including circulating tumor DNA and microRNAs, represent promising biomarkers for CRC detection and monitoring. MSI and MMR-related frameshift mutations arise early during tumorigenesis and may be detected by liquid biopsy, while circulating miRNAs are highly stable and become dysregulated during early CRC development. Stool represents a non-invasive source of tumor-derived DNA, miRNAs, and microbial signals directly related to colorectal epithelial biology. Analysis of fecal DNA may improve the detection of early MMR-deficient lesions by identifying characteristic frameshift mutations, while fecal miRNA and gut microbiome profiling may provide complementary signatures associated with colorectal carcinogenesis.

Preliminary institutional data from study INT 118/21 support the feasibility of liquid biopsy-based MSI analysis and miRNA profiling in LS patients undergoing endoscopic surveillance. These findings provide the rationale for a larger prospective observational study integrating plasma-, stool-, and urine-based molecular biomarkers with standard surveillance colonoscopy.

Study design and procedures: this is a prospective, longitudinal, observational study enrolling adult patients (≥18 years) with genetically confirmed Lynch Syndrome followed at the Unit of Hereditary Digestive Tract Tumors, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Participants are followed for 24 months and undergo surveillance colonoscopy at baseline (T0), after 12 months (T1), and after 24 months (T2), according to international guideline recommendations. At each scheduled colonoscopy visit, blood, urine, and stool samples are collected before bowel preparation and/or the endoscopic procedure. In addition, venous blood samples are collected every 3 months throughout the study, for a total of 12 blood collections per participant. A clinical evaluation is performed at each scheduled endoscopic visit. Dietary habits are assessed at T0, T1, and T2 using the validated EPIC dietary questionnaire.

Colonoscopy findings and, when available, histopathological results are recorded in a dedicated study database. Formalin-fixed paraffin-embedded tissue specimens obtained during routine clinical care are collected for possible additional translational analyses, including immunohistochemical assessment of MMR protein expression and/or MSI testing, when appropriate. Additional colonoscopies may be performed if clinically indicated.

MSI analysis is performed by digital PCR using the BAT25, BAT26, NR21, NR24, and Mono27 loci on ctDNA extracted from plasma samples. Plasma and stool miRNA profiling is performed by next-generation sequencing. Frameshift mutations are investigated in DNA extracted from stool samples using targeted sequencing of recurrent MMR deficiency-associated coding mononucleotide repeat mutations previously identified in MSI-high tumors. Stool microbiome analysis is performed by shotgun sequencing. Cell-free DNA extracted from urine samples is stored at -20°C for future exploratory analyses.

Objective: To evaluate the feasibility and diagnostic performance of plasma-, stool-, and urine-based molecular biomarkers for the early detection of colorectal precancerous and cancerous lesions in individuals with Lynch syndrome undergoing routine endoscopic surveillance, including MSI analysis in plasma ctDNA, plasma and stool miRNA profiling, fecal ctDNA frameshift mutation analysis, stool microbiome profiling, and exploratory urine cell-free DNA banking.

Being tested
Study procedures
Keywords
Lynch Syndrome, Mismatch Repair Deficiency, MicroSatellite Instability, circulating tumor DNA, Liquid biopsy, Plasma biomarkers, microRNA, frameshift mutations, Colorectal cancer surveillance, Colonoscopy, Microbiome
Medical subject headings
Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal Neoplasms, Turcot syndrome, Microsatellite Instability

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Study proceduresOther

    1. Standard-of-care surveillance colonoscopy performed according to international guidelines at T0, T1 (12 months), and T2 (24 months), with additional colonoscopies if clinically indicated;
    2. Collection of venous blood samples at each visit plus additional blood draws every 3 months, for a total of 12 blood collections per participant over the study. Plasma is isolated for extraction of circulating tumor DNA for MSI analysis by digital PCR and for miRNA analysis;
    3. Collection of a urine sample at each visit for future exploratory biomarker analyses;
    4. Collection of a stool sample at each visit for miRNA profiling, microbiome analysis, and fecal ctDNA frameshift mutation analysis;
    5. Collection of paraffin-embedded biopsy material for possible future immunohistochemical analysis of mismatch repair proteins and/or molecular MSI testing;
    6. Clinical evaluation at each scheduled colonoscopy visit and collection of dietary habits using the validated EPIC questionnaire.
Study groups in NCT07838246
Study groupRoleWhat they receive
Single CohortPatients with a confirmed pathogenic germline mismatch repair gene mutation (Lynch Syndrome) undergoing surveillance colonoscopy. There is no comparator or control arm; comparisons are made within the same cohort based on colonoscopy and histology findings.
Receives: Other: Study procedures

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Plasma ctDNA Microsatellite Instability and colorectal lesions

    Association between microsatellite instability in plasma ctDNA and the presence of colorectal lesions in LS patients.

    Measured: Over the 24-month observation period (T0, T1 at 12 months, T2 at 24 months).

  2. miRNA Profiles and colorectal lesions

    Diagnostic and predictive value of miRNA profiles for the presence of colorectal lesions in LS subjects.

    Measured: Over the 24-month observation period (T0, T1 at 12 months, T2 at 24 months).

  3. Gut microbial signatures and colorectal lesions

    Diagnostic and predictive value of gut microbial signatures for the presence of colorectal lesions in LS subjects.

    Measured: Over the 24-month observation period (T0, T1 at 12 months, T2 at 24 months).

  4. Fecal ctDNA frameshift mutations and colorectal lesions

    Association between fecal ctDNA frameshift mutations and the presence of colorectal lesions in LS patients.

    Measured: Over the 24-month observation period (T0, T1 at 12 months, T2 at 24 months).

Secondary outcomes (3)
  1. Urinary cell-free DNA collection and banking

    Collection and banking of cell-free DNA from urine samples for future exploratory analyses.

    Measured: At each colonoscopy visit (T0, T1, T2) over the 24-month observation period.

  2. Dietary habits assessment

    Collection of dietary habits using the validated EPIC questionnaire for future exploratory analyses of associations between diet, molecular biomarkers, microbiome features, and colorectal lesion occurrence.

    Measured: At each colonoscopy visit (T0, T1, T2) over the 24-month observation period.

  3. Stool microbiome profiles and colorectal lesions

    Exploratory evaluation of associations between stool microbiome profiles and colorectal lesion occurrence during the 24-month observation period.

    Measured: At each colonoscopy visit (T0, T1, T2) over the 24-month observation period.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Sep 2026
  2. Study start20 Jun 2023
  3. Primary completion25 Jun 2026
  4. Study completion25 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
109 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07838246
Sponsor's protocol ID
INT 73/23
Acronym
BioLynch
Status last verified
Aug 2026
First submitted
11 Sep 2026
Last updated
24 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified clinical and molecular individual participant data will be stored in a dedicated study database and may be shared for research purposes upon reasonable request, subject to approval by the Principal Investigator and in accordance with applicable institutional policies, ethics approvals, informed consent provisions, and data protection regulations.

Questions about this trial

What is this clinical trial studying?

An observational study of Lynch Syndrome and Hereditary Nonpolyposis Colorectal Cancer, run by Fondazione IRCCS Istituto Nazionale dei Tumori, Milano at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Plasma ctDNA Microsatellite Instability and colorectal lesions (time frame: Over the 24-month observation period (T0, T1 at 12 months, T2 at 24 months).). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Sep 2026.

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