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Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

Prognostic Impact of Adjuvant Therapy Following Surgical Resection in Primary Hepatic Sarcomatoid Carcinoma: A Retrospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06950814
Enrollment
50
Registered
2025-04-30
Start date
2025-04-05
Completion date
2025-05-05
Last updated
2025-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adjuvant Therapy, Liver Cancer, Sarcomatoid Carcinoma

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.

Interventions

PROCEDUREpostoperative adjuvant therapy

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.

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Disease-free survivalFrom December 2018 to May 2023Disease-free survival (DFS) was defined as the time from liver resection to disease recurrence or death from any cause.

Secondary

MeasureTime frameDescription
Overall survivalFrom December 2018 to May 2023Overall survival (OS) was defined as the interval from liver resection to death or the last follow-up.

Countries

China

Contacts

Primary ContactJiwei Huang Professor
huangjiwei@wchscu.cn+86 18980606725

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026