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Research on Precise Immune Prevention and Treatment of Glioma Based on Multi-omics Sequencing Data

Y

Yu Yao, MD

Status

Unknown

Conditions

Glioma
Radiomics
Transcriptomics

Treatments

Procedure: surgery

Study type

Observational

Funder types

Other

Identifiers

NCT04792437
KY2021-059

Details and patient eligibility

About

This project intends to use multiple types of biological samples from glioma patients and mouse intracranial tumor models as research objects, and comprehensively apply a series of omics sequencing technologies and molecular biology technologies to jointly define the following research objectives :

Full description

  1. Through high-throughput sequencing technologies such as, genome sequencing, transcriptome sequencing and single-cell sequencing, Proteomics,Metabonomics and Metagenomics, the similarities and differences of the glioma immune microenvironment within and between individuals were revealed from the multi-dimensional and big data level, and the immune molecular typing of glioma was established.
  2. Establish and verify that the neoantigen polypeptides predicted by AI algorithm after analyzing multi-omics data (genome, transcriptome, etc.) have good killing effect on individual tumor cells.
  3. To establish an intelligent evaluation model of glioma immunotyping by integrating imaging, pathology, high-throughput sequencing data and other omics information, and to provide a visual tool for monitoring changes in the intratumoral microenvironment of glioma patients, with the expectation of helping timely intervention of immunotherapy in patients with recurrence.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • The patients with glioma in the Department of Neurosurgery of Huashan Hospital Affiliated to Fudan University who meet the following three conditions can be enrolled

    1. They were 18-80 years old, male and female;

    2. The pathological diagnosis was glioma;

    3. On the basis of not affecting the clinical routine diagnosis, tissue (6 mm * 6 mm) or paraffin section (5 pieces) can be used for research;

    4. Sign informed consent or ethics committee approval

      Exclusion Criteria:

Trial design

120 participants in 1 patient group

glioma patients
Description:
glioma patients with routine surgery
Treatment:
Procedure: surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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