NCT07722819

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 21, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 13, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 13, 2026

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

July 19, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 23, 2026

Completed
Last Updated

July 23, 2026

Status Verified

July 1, 2026

Enrollment Period

3 months

First QC Date

July 19, 2026

Last Update Submit

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

Other: No intervention

Interventions

No intervention

Retrospective Cohort

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, 310022, China

Location

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

Locations