- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06204198
Clinicopathological Features and Molecular Typing of Invasive Fibroma of Abdominal Wall
January 11, 2024 updated by: Teng Qiong, Shandong Provincial Hospital
Analysis of Clinicopathological Features and Molecular Typing of Invasive Fibroma of Abdominal Wall and Construction of Recurrence Risk Model
Aggressive fibromatosis, also known as desmoid fibromatosis or desmoid tumor, is a fibrous tumor that occurs in the fascia, aponeurosis, or deep soft tissue and is formed by excessive proliferation of fibroblasts and myofibroblasts.
At present, the disease is considered to be a borderline tumor.
Due to the unclear boundary of the tumor, it often grows into the surrounding adjacent tissues, which is difficult to remove completely and easy to relapse.
It has been reported that nuclear β-catenin expression and CTNNB1 gene mutation can be used for the differential diagnosis of aggressive fibromatosis from other spindle cell lesions.
At present, there is a lack of multicenter retrospective clinical study of this disease, and there is no literature report on the postoperative quality of life of this kind of patients.
This study intends to further explore the clinicopathological features, prognosis and molecular typing of abdominal wall aggressive fibroma by retrospective analysis of the case data of multiple hospitals, as well as sequencing analysis of the retained specimens and paraffin specimens from previous operations, to study the high risk factors for recurrence of the disease, and to further comprehensively analyze the impact of abdominal wall aggressive fibroma surgery on the quality of life of patients through follow-up.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
The data of all patients with abdominal wall aggressive fibroma were collected through the medical record system of the hospital, and the molecular characteristics of the disease were analyzed by sequencing of the specimens retained by previous surgery or paraffin specimens.
The quality of life of patients was investigated by telephone or wechat follow-up to analyze the impact of postoperative disease on the quality of life of patients.
As a retrospective and observational study, the data of this study will be statistically summarized according to the following general principles.
Categorical data will be summarized descriptively using statistics including frequency n and percentage %, with 95% confidence intervals for overall percentages when necessary, and compared by chi-square or Fisher's exact test.
Continuous data will be statistically described as mean ± standard deviation or median (min, Max) and compared by Mann-Whitney (U) test or t-test.
The Kaplan-Meier method was used to estimate the survival function for time-to-event data, and survival curves were drawn to estimate the median time and 95% confidence intervals.
The differences between groups were compared with the use of the Log-rank test.
Cox proportional hazards model was used for univariate and multivariate analysis to screen independent prognostic factors related to recurrence, and the 95% confidence interval (CI) was recorded.
All statistical tests were performed with the use of a two-sided 0.05 level.
Statistical analysis will be calculated using SPSS 25 statistical analysis software.
Study Type
Observational
Enrollment (Estimated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Qiong Teng
- Phone Number: 18755138389
- Email: tengqiong2021@163.com
Study Locations
-
-
Shandong
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Jinan, Shandong, China, 250000
- Recruiting
- Shandong Provincial Hospital
-
Contact:
- Ronghua Zhang, MD
- Phone Number: +8618800187833
- Email: zhangrh91@126.com
-
Sub-Investigator:
- Qiong Teng
-
Principal Investigator:
- Yulong Shi
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who underwent resection at our hospital for aggressive fibroma in the abdominal wall.
Description
Inclusion Criteria:
- ① Surgical treatment for "invasive fibroma of abdominal wall"; ② Complete clinical data; ③ Agree to participate in the project.
Exclusion Criteria:
- ① can not cooperate with the project implementation; ② There is cognitive dysfunction; Refuse to participate in research projects.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinicopathological features checklist
Time Frame: From September 2023 to September 2024
|
Clinicopathological features
|
From September 2023 to September 2024
|
|
Postoperative survival of patients
Time Frame: From September 2023 to September 2024
|
Prognosis
|
From September 2023 to September 2024
|
|
Scores of patients' quality of life after surgery
Time Frame: From September 2023 to September 2024
|
Patients' quality of life after surgery
|
From September 2023 to September 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Yulong Shi, MD, Shandong Provincial Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2023
Primary Completion (Estimated)
February 1, 2024
Study Completion (Estimated)
September 1, 2024
Study Registration Dates
First Submitted
January 3, 2024
First Submitted That Met QC Criteria
January 11, 2024
First Posted (Actual)
January 12, 2024
Study Record Updates
Last Update Posted (Actual)
January 12, 2024
Last Update Submitted That Met QC Criteria
January 11, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SWYX:NO.2023-601
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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