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Immunotherapy Combined with Radiation for Unresectable Hepatocellular Carcinoma

Safety and Efficacy of Immunotherapy Combined with Radiation for Unresectable Hepatocellular Carcinoma

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1061240087
Enrollment
10
Registered
2024-12-10
Start date
2026-02-17
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular carcinoma

Interventions

Radiation therapy will be added for patients who have been induction treated with atezolizumab bevacizumab for hepatocellular carcinoma and who have reached SD/PD status by RECICT v1.1 criteria.

Sponsors

Takeuchi Yasuto
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Persons who are 18 years of age or older at the time of obtaining consent (2) Male or female (3) PS 0 or 1 (4) Patients diagnosed with SD or PD based on RECIST ver.1.1 after starting treatment with atezolizumab or bevacizumab (5) Patients with at least one intrahepatic target lesion based on RECIST ver. 1.1 (6) Patients with no history of systemic drug therapy or radiation therapy for hepatocellular carcinoma (7) Patients must be confirmed disease-free for at least 6 months after the last administration of postoperative adjuvant drug therapy (7) Patients with Child Pugh class A (8) Subjects who have received a thorough explanation of the study and who have given their consent to participate in the study in writing of their own free will after full understanding of the study

Exclusion criteria

Exclusion criteria: (1) Patients with hepatocellular carcinoma occupying more than 50% of the liver volume (2) Patients with allergy to CT/MRI contrast media (3) Patients with estimated glomerular filtration rate (eGFR) < 30 (4) Patients with active multiple cancers (5) Other subjects who are judged by the principal investigator and the subinvestigators to be inappropriate as research subjects due to the disease status of the tumor, difficulty in induction of chemotherapy, or other reasons.

Design outcomes

Primary

MeasureTime frame
Adverse event

Secondary

MeasureTime frame
(1) Response rate (2) Progression-free survival (3) Duration of response

Contacts

Public ContactYasuto Takeuchi

Okayama University Hospital

yasuto19800125@okayama-u.ac.jp+81-86-235-7219

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026