Bo Chen
Beijing, China
Location status: Recruiting
Location contact
Bo Chen
CONTACT
Bo Chen
PRINCIPAL_INVESTIGATOR
Yirui Zhai
SUB_INVESTIGATOR
NCT Number: NCT06205472
This is a single-arm prospective phase II clinical trial to investigate the efficacy and safety of adjuvant simultaneouslyintegrated boost radiotherapy following narrow-margin(<1cm) hepatectomy in patients with HCC. Eligibility patients will receive IMRT or VMAT to high risk area of tumor bed and tumor bed. The prescription dose to 95% GTVtb boost was planned at 55-60Gy, with PTV 45-50Gy, in 23-25 fractions, mainly depending on the dose constraints of OARs. The primary endpoint is the 3-year OS, the secondary endpoints are disease-free survival, patterns of failure, toxic events and local control rate.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Beijing, China
Location status: Recruiting
Bo Chen
CONTACT
Bo Chen
PRINCIPAL_INVESTIGATOR
Yirui Zhai
SUB_INVESTIGATOR
Surgical resection is the primary treatment for HCC. However, it is associated with a high rate of recurrence and death. Based on the results of our retrospective study and phase II study, adjuvant radiotherapy is an effective, tolerable, and promising adjuvant regimen in patients with narrow-margin(<1cm) after hepatectomy. The 3-year and 5-year OS rates of 88.2% and 72.2% were significantly higher than the expected rates based on published reports and exceeded our predetermined threshold. However, there is no standard for the prescription dose. The high risk area of recurrence is mostly close to the blood vessels in the tumor bed, and simultaneously integrated boost (SIB) technique can optimize the target dose while protecting normal tissues. So, the investigators conducted this single-arm prospective phase II clinical trial to investigate the efficacy and safety of adjuvant SIB radiotherapy following narrow-margin(<1cm) hepatectomy in patients with HCC.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Eligibility patients will receive IMRT or VMAT to high risk area of tumor bed and tumor bed. The prescription dose to 95% GTVtb boost was planned at 55-60Gy, with PTV 45-50Gy, in 23-25 fractions,mainly depending on the dose constraints of OARs.
Time frame: up to 36 months
The 3-year overall survival was calculated from the date of surgical resection to the date of death from any cause.
Time frame: up to 36 months
Disease-free survival (DFS) was calculated from the date of surgical resection to the date of the first recurrence or death from HCC
Time frame: up to 36 months
The type of recurrence (locoregional failures or distant failure)
Time frame: up to 36 months
Toxic events was evaluated during received protocol therapy according to CTCAE 4.03
Time frame: up to 36 months
Patients with stable disease [SD], partial response [PR] or complete response[CR] were recorded as local control.
Contact information is provided by the study sponsor or research team.
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Other
Phase II Study of Adjuvant Simultaneously Integrated Boost Radiotherapy Following Narrow-Margin Hepatectomy in Patients With HCC.
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.
Published trials that share one or more normalized conditions with this study.
NCT07062055
Adenocarcinoma, Carcinoma
Jinan, Shandong, China
View Trial DetailsNCT06864221
Adenocarcinoma, Biomarkers
Guangzhou, Guangdong, China
View Trial DetailsNCT06389422
Adenocarcinoma, Carcinoma
Beijing, Beijing Municipality, China
View Trial DetailsNCT06261047
Adenocarcinoma, Carcinoma
Jinan, Shandong, China
View Trial Details