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Impact of Emotional Disorders on Response to Immune Checkpoint Inhibitor Therapy in Liver Cancer: A Multicenter, Prospective, Multi-Cohort Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Hepatocellular carcinoma (HCC) carries a poor prognosis, with limited efficacy from current therapies including immune checkpoint inhibitors (ICIs). Concurrently, emotional distress (ED) is highly prevalent in cancer patients and is implicated in tumor progression via neuroendocrine-immune axis dysregulation (e.g., HPA axis activation, immunosuppressive TME). Emerging evidence, particularly from lung cancer, suggests ED may adversely impact ICI efficacy. However, its specific role and clinical significance in HCC, especially regarding ICI response, remain poorly understood. To address this gap, we propose a large-scale, prospective, multicenter, multi-cohort study to systematically evaluate the impact of ED on treatment outcomes in HCC patients receiving immunotherapy.

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

• Age between 18 and 75 years, inclusive, regardless of gender.

• Presence of at least one radiologically measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 (defined as a lesion with a longest diameter of ≥10 mm on CT scan).

• Newly diagnosed, treatment-naïve patients with hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (ICC).

• Child-Pugh liver function score ≤ 7.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

• Absence of severe organic diseases affecting the heart, lungs, brain, or other major organs.

Locations
Other Locations
China
Division of Hepato-Pancreato-Biliary Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
RECRUITING
Wuhan
Contact Information
Primary
Wanguang Zhang
wgzhang@tjh.tjmu.edu.cn
13886195965
Time Frame
Start Date: 2025-12-20
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 651
Treatments
Advanced unresectable HCC cohort
Cohort 1: Impact of ED on first-line therapy for advanced, unresectable HCC (n=243)
Advanced unresectable ICC cohort
Cohort 2: Impact of ED on first-line therapy for advanced, unresectable intrahepatic cholangiocarcinoma (ICC) (n=175)
Resectable high-risk HCC cohort
Cohort 3: Impact of ED on postoperative recurrence in resectable high-risk HCC (n=233)
Related Therapeutic Areas
Sponsors
Leads: Tongji Hospital

This content was sourced from clinicaltrials.gov

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