Skip to content

Prospective Multicenter Registry Study to Assess the Frequency of Lynch Syndrome Among Patients With Colorectal Cancer

Prospective Multicenter Registry Study to Assess the Frequency of Lynch Syndrome Among Patients With Colorectal Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05495776
Acronym
MSIRus22
Enrollment
2500
Registered
2022-08-10
Start date
2022-08-01
Completion date
2028-12-31
Last updated
2022-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Hereditary Colorectal Cancer, Lynch Syndrome, MSI

Keywords

Colorectal Cancer, Lynch Syndrome, Hereditary Colorectal Cancer, MSI, Frequency

Brief summary

Prospective multicenter registry study to assess the frequency of Lynch syndrome among patients with colorectal cancer in Russia

Detailed description

Blood and tumor samples will be obtained from enrolled patients. 4 ml of venous blood samples will be taken into a tube with EDTA and stored at -20 0C. Tumor samples will be taken during endoscopy or surgical treatment, embedded in paraffin and stored at room temperature. Microsatellite instability in the tumor tissue will be determined by any method available in the participating center (immunohistochemical or molecular genetic study). In case of detection of microsatellite instability/deficiency in the repair system of unpaired bases blood samples will be analyzed for the fact that germinal mutations in the DNA mismatch repair genes. Patients will be followed up for 5 years after enrollment. During follow up correlation of spectrum of germinal mutations with clinical data, effectiveness of therapy with immune checkpoint inhibitors, the spectrum of malignant neoplasms in the families of patients with Lynch syndrome, the impact of the presence of microsatellite instability/deficiency in the DNA mismatch repair genes on treatment tactics in the Russian Federation will be assessed.

Interventions

None listed

Sponsors

The Loginov MCSC MHD
CollaboratorUNKNOWN
Pirogov National Medical and Surgical Center
CollaboratorUNKNOWN
Moscow City Oncological Hospital No. 62 MHD
CollaboratorUNKNOWN
City Clinical Oncological Hospital No. 1 MHD
CollaboratorUNKNOWN
MMCC Kommunarka MHD
CollaboratorUNKNOWN
D.D. Pletnev City Clinical Hospital MHD
CollaboratorUNKNOWN
Botkin Hospital MHD
CollaboratorUNKNOWN
Clinic K+31
CollaboratorUNKNOWN
State Scientific Centre of Coloproctology, Russian Federation
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Provision of written informed consent; * Patients with histologically verified colon adenocarcinoma or patients with histologically verified synchronous neoplasms who have not previously received treatment for a second tumor; * Age ≥ 18 years; * Absence of antitumor treatment for a real tumor (it is allowed to include patients who have a history of antitumor treatment for other malignant tumors, if the period after treatment is more than 12 months). * The ability of the patient, according to the Researcher, to fulfill the requirements of the Protocol;

Exclusion criteria

\- Patients receiving chemotherapy or radiotherapy for colon cancer at the time of screening

Design outcomes

Primary

MeasureTime frameDescription
Frequency of microsatellite instability and Lynch syndromeup to 5 yearsTo assess the frequency of microsatellite instability and Lynch syndrome in the population of patients with colorectal cancer in the Russian Federation.

Secondary

MeasureTime frameDescription
Frequency of occurrence of microsatellite instability/deficiencyup to 5 yearsAssessment of the frequency of occurrence of microsatellite instability/deficiency in the repair system of unpaired bases in second tumors in patients with colorectal cancer of various stages.
Spectrum of germinal mutations in Lynch syndromeup to 5 yearsThe mlh1, msh2, msh6, pms2 and epcam genes will be examined for the presence of all types of pathogenic variants in patients with MSI in colon tumor. The possible correlation of gene-phenotype and pathogenic variants of each gene-phenotype will also be studied. To detect MSI in a tumor sample, need to do the fragment analysis (markers NR21, NR24, NR27, BAT25, BAT26). Рatients with MSI in the tumor will have DNA diagnostics of MMR EPCAM genes by sequencing and MLPA . The MMR and EPCAM genes will be examined in DNA isolated from blood lymphocytes.
Spectrum of malignant neoplasmsup to 5 yearsThe family history of all oncological diseases will be studied to find out the main target organs of patients with Lynch syndrome in Russia
Effectiveness of therapy with immune checkpoint inhibitorsup to 5 yearsThe frequency will be compared: the frequency of objective response rate (RECIST 1.1) while using immune checkpoint inhibitors in metastatic colon cancer and microsatellite instability associated/not associated with Lynch syndrome
Impact of the presence of microsatellite instability/deficiencyup to 5 yearsThe frequency of adjuvant chemotherapy in stages II-III of colon cancer in the presence of microsatellite instability / deficiency in the repair system of unpaired bases in real clinical practice will be evaluated

Countries

Russia

Contacts

Primary ContactDmitrii Semenov, PhD
dr.semenov@inbox.ru+7 (985) 2632870
Backup ContactAlexey Tsukanov, PhD
tsukanov81@rambler.ru+7 (916) 7563957

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 20, 2026