Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma
1 other identifier
observational
50
1 country
1
Brief Summary
In recent years, researchers have conducted extensive studies on adjuvant therapy following surgical resection of liver cancer, exploring its potential benefits and seeking effective treatment strategies. Given the rarity and high aggressiveness of primary hepatic sarcomatoid carcinoma, there is a lack of reliable clinical evidence on whether postoperative adjuvant therapy can benefit patients, resulting in the absence of established standard guidelines. Therefore, we conducted a single-center retrospective study to assess the potential benefits of postoperative adjuvant therapy for patients of primary hepatic sarcomatoid carcinoma.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2025
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 5, 2025
CompletedFirst Submitted
Initial submission to the registry
April 22, 2025
CompletedFirst Posted
Study publicly available on registry
April 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 3, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 5, 2025
CompletedApril 30, 2025
April 1, 2025
28 days
April 22, 2025
April 22, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Disease-free survival
Disease-free survival (DFS) was defined as the time from liver resection to disease recurrence or death from any cause.
From December 2018 to May 2023
Secondary Outcomes (1)
Overall survival
From December 2018 to May 2023
Study Arms (2)
Primary hepatic sarcomatoid carcinoma patients who received adjuvant therapy
Primary hepatic sarcomatoid carcinoma patients who did not receive adjuvant therapy
Interventions
Given the rarity and high aggressiveness of PHSC, there is a lack of reliable clinical evidence on whether postoperative adjuvant therapy can benefit patients, resulting in the absence of established standard guidelines.
Eligibility Criteria
The data was collected from patients who underwent liver resection and were diagnosed with PHSC pathologically. The data was collected from the division of Liver Surgery of West China Hospital, SCU from December 2018 to May 2023.
You may qualify if:
- patients who underwent liver resection
- patients' postoperative paraffin pathology and immunohistochemistry results were reviewed to identify those diagnosed with PHSC
You may not qualify if:
- patients who received other anti-tumor treatments before surgery, such as radiofrequency ablation (RFA), transarterial chemoembolization (TACE), radiation therapy (RT), and systemic therapy;
- patients diagnosed with other specific types of sarcomas;
- patients with concurrent other malignancies during the course of PHSC;
- patients who were lost to follow-up or lacked essential clinical data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
West China Hospital
Chengdu, Sichuan, 610041, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Professor
Study Record Dates
First Submitted
April 22, 2025
First Posted
April 30, 2025
Study Start
April 5, 2025
Primary Completion
May 3, 2025
Study Completion
May 5, 2025
Last Updated
April 30, 2025
Record last verified: 2025-04
Data Sharing
- IPD Sharing
- Will not share