NCT06950814

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

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Apr 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

April 22, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 30, 2025

Completed
3 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 3, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 5, 2025

Completed
Last Updated

April 30, 2025

Status Verified

April 1, 2025

Enrollment Period

28 days

First QC Date

April 22, 2025

Last Update Submit

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

Procedure: postoperative 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.

Primary hepatic sarcomatoid carcinoma patients who received adjuvant therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

CarcinomaLiver Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Central Study Contacts

Jiwei Huang Professor

CONTACT

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

Locations