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Recruiting NCT06950814

Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

Observational Sarcomatoid Carcinoma Liver Cancer Adjuvant Therapy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: postoperative adjuvant therapy.
Who it may be relevant to
Registry conditions: Sarcomatoid Carcinoma, Liver Cancer, Adjuvant Therapy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Procedure postoperative 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.

Primary outcome measures

  • Disease-free survival [Time frame: From December 2018 to May 2023]
Secondary outcome measures (1)
  • Overall survival [Time frame: From December 2018 to May 2023]

Eligibility criteria

Inclusion criteria

  • patients who underwent liver resection
  • patients' postoperative paraffin pathology and immunohistochemistry results were reviewed to identify those diagnosed with PHSC

Exclusion criteria

  • 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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • West China Hospital — Chengdu

Identifiers

NCT: NCT06950814 · JHuang20231

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗