Efficacy and Safety of Radiotherapy in Oligoprogressive HCC Following First-line PD-1 Therapy: A Phase II Clinical Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Immune checkpoint inhibitors (ICIs) have significantly improved the survival outcomes of HCC patients. However, a considerable proportion of patients eventually experience disease progression due to the development of resistance. Among these, oligoprogression is a common manifestation, occurring in 10-55.3% of advanced cancer patients. Local therapy, especially radiotherapy (RT), has been increasingly considered in the setting of oligoprogression to overcome ICIs resistance and delay the need to change systemic therapy. Therefore, this study aimed to explore the efficacy and safety of RT in oligoprogressive HCC following first-line PD-1 therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Diagnosis of hepatocellular carcinoma (HCC) based on either histopathologic or cytologic findings or a diagnosis of cirrhosis and HCC with classical imaging characteristics;

• HCC patients with oligoprogression after first-line PD-1 therapy ;

• Stable Disease for at least 3 months after first-line PD-1 therapy ;

• Oligoprogressive disease in 5 or fewer lesions and 3 or fewer organs

• Tumor staged as BCLC stage C

• ECOG performance status: 0-1.

• Life expectancy \>=6 months.

• No history of irradiation.

• aged 18 to 75 years old are eligible.

⁃ Patients must be able to understand and willing to sign a written informed consent document.

⁃ Female patients within childbearing age or male patients whose sexual partners are women within childbearing age need to take effective contraceptive measures throughout the treatment period and 6 months after the treatment.

Locations
Other Locations
China
Zhongshan Hospital, Fudan University
RECRUITING
Shanghai
Contact Information
Primary
Shu-jung Hsu
21111210002@m.fudan.edu.cn
+8613585805072
Backup
Shi-suo Du
du.shisuo@zs-hospital.sh.cn
+8613916988702
Time Frame
Start Date: 2022-07-28
Estimated Completion Date: 2025-12
Participants
Target number of participants: 35
Treatments
Experimental: Maintenance first-line treatment plus radiation therapy
Related Therapeutic Areas
Sponsors
Leads: Shanghai Zhongshan Hospital

This content was sourced from clinicaltrials.gov