The Second Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, 510260, China
Location status: Recruiting
Location contact
Kangshun Zhu, Dr.
CONTACT
Kangshun Zhu, Dr.
PRINCIPAL_INVESTIGATOR
Mingyue Cai, Dr.
SUB_INVESTIGATOR
NCT Number: NCT05994859
This study is conducted to evaluate the efficacy and safety of Y-90 selective internal radiation therapy (SIRT) in patients with potentially resectable hepatocellular carcinoma (HCC).
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Guangzhou, Guangdong, 510260, China
Location status: Recruiting
Kangshun Zhu, Dr.
CONTACT
Kangshun Zhu, Dr.
PRINCIPAL_INVESTIGATOR
Mingyue Cai, Dr.
SUB_INVESTIGATOR
This is a bi-center, prospective study to evaluate the efficacy and safety of SIRT in patient with potentially resectable HCC.
35 patients with potentially resectable (initially unresectable) HCC will be enrolled in this study. The patients will receive 1-2 sessions of SIRT. If the patients have invasive tumors, extensive liver involvement or vascular invasion, systematic treatment will be added. If the patients are evaluated as resectable during follw-up, liver resection will be recommended.
The primary end point of this study is success rate of conversion to resection. The secondary endpoints are objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), time to progression (TTP), duration of response (DOR), overall survival (OS) and adverse events (AEs).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The patients will receive 1-2 sessions of SIRT. If the patients have invasive tumors, extensive liver involvement or vascular invasion, systematic treatment will be added.
Time frame: 3 years
The proportion of patients with initially unresectable HCC who were evaluated by the surgical team as suitable for second-stage surgical resection after SIRT
Time frame: 3 years
The percentage of patients who have a best overall tumor response rating of complete response (CR) or partial response (PR)
Time frame: 3 years
The percentage of patients who have a tumor response rating of CR, PR, or stable disease (SD)
Time frame: 3 years
The time between the first treatment and the first occurrence of disease progression (PD) or death from any cause, whichever occurs first
Time frame: 3 years
the time interval from first treatment to the first occurrence of disease progression
Time frame: 3 years
the time from initial objective response (CR or PR) until PD or death, whichever occurs first
Time frame: 3 years
The time from initiation of treatment until the date of death from any cause
Time frame: 3 years
Number of patients with AEs assessed by NCI CTCAE v5.0.
Contact information is provided by the study sponsor or research team.
Kangshun Zhu, Dr.
CONTACT
Mingyue Cai, Dr.
CONTACT
Second Affiliated Hospital of Guangzhou Medical University
Other
Y-90 Selective Internal Radiation Therapy for Potentially Resectable Hepatocellular Carcinoma: a Prospective, Single Arm Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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