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NCT Number: NCT06521684

Translational Study of MSS, TP53 Mutation and Chromosome Instability Relationship in Endometrial Carcinoma

The objective is to understand the relationship between TP53 mutation, MSS and chromosome instability in endometrial cancer and the effect on clinical prognosis.We will collect a small amount of tumor tissue samples. NGS panel detection and WGD/AS analysis were performed on the tissue. Paracancer tissue was used as a negative control and relevant information in medical records during the operation. Then we will collect clinical diagnosis and disease information through telephone follow-up after the completion of the operation.

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Key information

About this study

The test is sequenced using Illumina high-throughput sequencers and accompanying kits. Conduct preliminary quality control on the samples, and the tumor cell content of the tissue samples shall not be less than 30%. Tissue DNA was extracted from tumor tissue samples according to the instructions of the QIAGEN DNA extraction kit. Samples qualified for quality control shall be arranged for further library construction. The extracted DNA samples were sequentially purified by fragment purification, terminal repair, splicing, fragment size selection, PCR amplification, product purification, library enrichment, and library product quality control. After qualified quality control, the constructed library was sequenced by Illumina matching kit. Bioinformatics analysis would be conducted.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • willing to participate in the study and sign the informed consent
  • age ≥18 years old
  • researchers evaluated that it was suitable to participate in this translational study
  • Endometrial cancer was confirmed histologically
  • histopathological molecular classification was consistent with pMMR type and POLE wild type
  • The tumor tissue obtained by operation was the primary lesion

Exclusion criteria

  • Received chemotherapy within 14 days prior to sample collection, or received anti-tumor drug therapy such as radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy, within 21 days prior to sample collection
  • previously treated with KIF18A inhibitors
  • researchers believed that the subjects were not suitable for the translational study for other reasons

Treatment and study plan

Primary outcomes

  1. microsatellite stability status

    Time frame: 2025-06-30

    microsatellite stability status

  2. TP53 mutation

    Time frame: 2025-06-30

    TP53 mutation

  3. Chromosomal instability

    Time frame: 2025-06-30

    Chromosomal instability (Whole genome duplication, Aneuploidy)

Secondary outcomes

  1. recurrence

    Time frame: 2026-06-30

    disease recur

Sponsors and collaborators

Lead sponsor

Peking Union Medical College Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jul 26, 2024
Registry last updated
Jul 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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