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Recruiting NCT06950814

NCT06950814 Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

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Clinical Trial Summary
NCT ID NCT06950814
Status Recruiting
Phase
Sponsor West China Hospital
Condition Sarcomatoid Carcinoma
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2025-04-05
Primary Completion 2025-05-03

Trial Parameters

Condition Sarcomatoid Carcinoma
Sponsor West China Hospital
Study Type OBSERVATIONAL
Phase N/A
Enrollment 50
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-04-05
Completion 2025-05-03
Interventions
postoperative adjuvant therapy

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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.

Eligibility Criteria

Inclusion Criteria: 1. patients who underwent liver resection 2. patients' postoperative paraffin pathology and immunohistochemistry results were reviewed to identify those diagnosed with PHSC Exclusion Criteria: 1. patients who received other anti-tumor treatments before surgery, such as radiofrequency ablation (RFA), transarterial chemoembolization (TACE), radiation therapy (RT), and systemic therapy; 2. patients diagnosed with other specific types of sarcomas; 3. patients with concurrent other malignancies during the course of PHSC; 4. patients who were lost to follow-up or lacked essential clinical data.

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