A Post Approval Study to Evaluate Safety and Effectiveness of Multicompartmental Dosimetry Planning.
NCT07669727
Adenocarcinoma, Carcinoma
View Trial DetailsNCT Number: NCT07206511
This is a prospective cohort study designed to evaluate the effectiveness and safety of two post-conversion treatment strategies for patients with initially unresectable hepatocellular carcinoma (uHCC). Participants first receive conversion therapy with transarterial chemoembolization (TACE) or hepatic arterial infusion chemotherapy (HAIC) combined with anti-angiogenic agents and immune checkpoint inhibitors (ICIs). After this therapy, patients who achieve complete radiological response (rCR) or meet resectability criteria will either undergo surgical resection or continue systemic therapy. The study aims to compare outcomes between these two strategies to help guide treatment decisions for advanced liver cancer.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From initiation of post-conversion therapy to the first documented event (recurrence, progression, or death), up to 36 months
Defined as the time from the date of achieving rCR or resectability criteria to the time of becoming inoperable, recurrence, progression, or death from any cause for uHCC patients.
Time frame: 2 years after initiation of post-conversion therapy
Defined as the rate of no events (recurrence, progression, or death from any cause) occurring in rCR patients over 2 years.
Time frame: Up to 36 months after initiation of post-conversion therapy
Defined as the survival time from the day of achieving rCR to death from any cause。
Time frame: From initiation of post-conversion therapy through 30 days after last treatment or surgery, up to 36 months follow-up
: The incidence of adverse events in the surgery group and the systemic therapy group. Adverse events recorded on the CRF will be mapped to preferred terms using the Medical Dictionary for Regulatory Activities (MedDRA). Severity, seriousness/grade, and the relationship with the study treatment will be assessed by the investigators. The seriousness/grade will be defined according to the National Cancer Institute (NCI) CTCAE v5.0.
Time frame: Up to 36 months after initiation of post-conversion therapy
The cost-effectiveness ratio (C/E) is defined as the ratio of time to an event (EFS) or overall survival (death) from rCR to all direct costs (medical expenses, including outpatient and inpatient), and will be compared between the two groups.
Contact information is provided by the study sponsor or research team.
Shanghai Zhongshan Hospital
Other
Clinical Outcomes of Initially Unresectable Hepatocellular Carcinoma Patients Receiving TACE/HAIC Plus Anti-Angiogenic Agents and Immune Checkpoint Inhibitors as Conversion Therapy, Achieving Complete Radiological Response or Resectability, Followed by Systemic Treatment or Surgical Resection: A Prospective Cohort Study
Acronym: THAI-CONVERT
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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