Actively Recruiting

Age: 18Years +
All Genders
NCT06950814

Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

Led by West China Hospital · Updated on 2025-04-30

50

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who underwent liver resection
  • Patients diagnosed with primary hepatic sarcomatoid carcinoma confirmed by postoperative pathology and immunohistochemistry
Not Eligible

You will not qualify if you...

  • Patients who received other anti-tumor treatments before surgery such as radiofrequency ablation, transarterial chemoembolization, radiation therapy, or systemic therapy
  • Patients diagnosed with other specific types of sarcomas
  • Patients with other concurrent malignancies during the course of PHSC
  • Patients who were lost to follow-up or lacked essential clinical data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

West China Hospital

Chengdu, Sichuan, China, 610041

Actively Recruiting

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Research Team

J

Jiwei Huang Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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