RecruitingNCT07464470

Comparison of Molecular-Genetic Concordance of the Primary Tumor and Brain Metastases of Gastroesophageal Cancers

Comparison of Molecular-Genetic Concordance of the Primary Tumor and Brain Metastases of Gastroesophageal Cancers (GENCONCOR-2)


Sponsor

Blokhin's Russian Cancer Research Center

Enrollment

30 participants

Start Date

Apr 1, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

GENCONCOR-2 is a translational research aimed to compare the molecular profile of primary tumors and their matched brain metastases in gastroesophageal cancers, including cancer of the esophagus, gastroesophageal junction, and stomach. The study is based on the previously established international GASTROBRAIN cohort (ClinicalTrials.gov ID: NCT07448493), which provides comprehensive clinicopathological and treatment data for over 230 patients. It will be conducted by retrospective analysis of paired samples of histological material (primary tumor and corresponding brain metastasis) with determination of HER2 expression status (IHC ± FISH), MSI status (IHC ± PCR), PD-L1 combined positive score (CPS), and CLDN18.2 expression status (IHC)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing the genetic makeup of stomach/esophageal (gastroesophageal) cancer tumors with the genetic makeup of brain metastases (cancer that has spread to the brain) from the same patients. The goal is to understand how the cancer evolves and changes when it spreads to the brain, which could inform future treatment decisions. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with gastric, esophageal, or gastroesophageal junction cancer - You have undergone surgery to remove a brain metastasis from this cancer - Preserved tumor tissue samples from both the original tumor and the brain metastasis are available **You may NOT be eligible if...** - You have another simultaneous or prior cancer from a different site - Your brain metastasis was not from a gastroesophageal cancer - Adequate tissue samples are not available for analysis Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTHER2 Testing

Assessment of HER2 status by immunohistochemistry (IHC) using SP3 antibody clone (DAKO) on Ventana GX platform with OptiView detection system. Cases with IHC 2+ will undergo confirmatory in situ hybridization (FISH, CISH, or SISH).

DIAGNOSTIC_TESTMSI Testing

Determination of microsatellite instability status by immunohistochemistry (IHC) for mismatch repair proteins (MLH1, MSH2, MSH6, PMS2) ± PCR-based analysis using five mononucleotide repeat markers (BAT25, BAT26, NR21, NR24, NR27).

DIAGNOSTIC_TESTPD-L1 Testing

Assessment of PD-L1 expression by immunohistochemistry (IHC) using DAKO 22C3 antibody clone on Dako Link48 platform with EnVision Flex detection system. Results reported as Combined Positive Score (CPS), defined as number of PD-L1-stained cells divided by total viable tumor cells, multiplied by 100.

DIAGNOSTIC_TESTCLDN18.2 Testing

Assessment of CLDN18.2 expression by immunohistochemistry (IHC) using VENTANA CLDN18 (43-14A) assay on Ventana platform. Positive expression defined as moderate-to-strong (2+/3+) complete, basolateral, or lateral membranous staining in ≥ 75% of viable tumor cells.


Locations(1)

Blokhin's Russian Cancer Research Center

Moscow, Russia

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NCT07464470


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