RecruitingNCT06405321

Conversion or Neoadjuvant Therapy in Hepatocellular Carcinoma

Conversion or Neoadjuvant Therapy in Hepatocellular Carcinoma: A Multicenter Retrospective Study in Guangxi, China (GUIDANCE)


Sponsor

Guangxi Medical University

Enrollment

2,000 participants

Start Date

Jan 1, 2019

Study Type

OBSERVATIONAL

Conditions

Summary

This multicenter retrospective study which included patients with hepatocellular carcinoma (HCC) who received conversion or neoadjuvant therapy to explore the best treatment options and the best benefit group.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria4

  • Histologically or clinically confirmed diagnosis of HCC.
  • Patients who received conversion or neoadjuvant therapy as initial treatment, including hepatic artery infusion chemotherapy (HAIC), transcatheter arterial chemoembolization (TACE), tyrosine kinase inhibitors (TKIs), immune checkpoint inhibitors (ICIs), or radiotherapy.
  • Eastern Cooperative Oncology Group performance status (ECOG-PS) of 0 or 1.
  • With Child-Pugh 5\~7 scores.

Exclusion Criteria3

  • Concurrent with other malignancies within 5 years.
  • Incomplete medical data.
  • Follow-up time less than 3 months.

Interventions

DRUGConversion or neoadjuvant therapy.

Patients with hepatocellular carcinoma received conversion or neoadjuvant therapy.


Locations(1)

Jian-Hong Zhong

Nanning, China, China

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NCT06405321


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