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Clinical Trials/NCT05171413
NCT05171413
Recruiting
Not Applicable

Predictive Models of Treatment Responses and Survival Outcomes in Patients With Soft Tissue Sarcoma

West China Hospital1 site in 1 country800 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Soft Tissue Sarcoma
Sponsor
West China Hospital
Enrollment
800
Locations
1
Primary Endpoint
Progression-free survival outcomes
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

The aim of this study was to developed and validated models to predict therapeutic responses and patients' survivals in patients with soft tissue sarcoma and compared these models with currently available models.

Detailed Description

We performed a retrospective-prospective cohort study with the aim of developing and validating comprehensive models to predict treatment responses and survival outcomes in patients with biopsy-proven soft tissue sarcoma. Secondly, we aimed to compare the predictive accuracy with currently available noninvasive model.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
December 31, 2024
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yuhan Yang

Associate Professor

West China Hospital

Eligibility Criteria

Inclusion Criteria

  • Receiving no treatment before diagnosis
  • With written informed consent

Exclusion Criteria

  • Clinical data missing
  • Without written informed consent

Outcomes

Primary Outcomes

Progression-free survival outcomes

Time Frame: At least 5-year follow up

The endpoint was defined as the occurrence of progression or recurrence, or the last follow-up. Patients were followed from the day of histological diagnosis until the occurrence of progression or recurrence, or last visit. The outcome was evaluated by an experienced oncologist in each center every 3-6 months. At each visit, a medical history, physical examination, and standard laboratory tests were performed.

Overall survival outcomes

Time Frame: At least 5-year follow up

The endpoint was defined as the occurrence of death or the last follow-up. Patients were followed from the day of histological diagnosis until the occurrence of progression or recurrence or last visit. The outcome was evaluated by an experienced oncologist in each center every 3-6 months. At each visit, a medical history, physical examination, and standard laboratory tests were performed.

Treatment response

Time Frame: At least 1-year follow up

The primary outcome was the evaluation of treatment response to individualized therapy in patients with soft tissue sarcoma.

Study Sites (1)

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