ESCC Molecular Subtypes Based on Multidimensional Features of p53 and Their Clinical Significance
2 other identifiers
observational
300
1 country
1
Brief Summary
Collect 300 esophageal cancer tissue specimens, including cancer tissue and serum, from a biological sample bank. Collect clinical information on esophageal cancer, including gender, age, time of diagnosis, time of death, treatment information, TNM staging, tumor size, location, etc. DNA sequencing was performed on 300 collected esophageal cancer samples, divided into mutant and wild-type types. Perform immunohistochemistry on tissue slices and observe the expression of P53 mutant protein. ELISA was used to study the expression of serum anti-P53 autoantibodies. Process these data and use them to classify subtypes of esophageal cancer. Associate each subtype with clinical information, analyze the characteristics of each subtype, such as the multidimensional features of P53 and treatment correlation analysis, and the correlation between P53 multidimensional features and survival.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 13, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 13, 2026
CompletedFirst Submitted
Initial submission to the registry
July 19, 2026
CompletedFirst Posted
Study publicly available on registry
July 23, 2026
CompletedJuly 23, 2026
July 1, 2026
3 months
July 19, 2026
July 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Time from surgery to death from any cause (for Overall Survival) or to disease recurrence/local-regional failure (for Recurrence-Free Survival).
Data collected up to December 31, 2024
Study Arms (1)
Retrospective Cohort
Interventions
Eligibility Criteria
This is a single-center, retrospective cohort study. The study population consists of histologically confirmed esophageal squamous cell carcinoma (ESCC) patients who underwent surgical resection at Zhejiang Cancer Hospital between 2015 and 2024. All patients had available p53 molecular data and complete clinical follow-up information.
You may qualify if:
- Histologically confirmed esophageal squamous cell carcinoma (ESCC); Age ≥ 18 years; Undergone surgical resection; Availability of p53 molecular data and clinical follow-up data.
You may not qualify if:
- Incomplete medical records or missing key clinicopathological data. Non-squamous histological types.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ling Zhiqianglead
Study Sites (1)
Zhejiang Cancer Hospital
Hangzhou, Zhejiang, 310022, China
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Prof., M.D., PhD,
Study Record Dates
First Submitted
July 19, 2026
First Posted
July 23, 2026
Study Start
April 21, 2026
Primary Completion
July 13, 2026
Study Completion
July 13, 2026
Last Updated
July 23, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share