The Impact of Emotional Stress on Immunotherapy Outcomes in Liver Cancer Patients: A Multi-Cohort Study
Recruiting now
Conditions studied: HCC - Hepatocellular Carcinoma, Psychological Distress, Immune Checkpoint Inhibitors (ICIs), Cancer, Treatment-Related, Unresectable Hepatocellular Carcinoma
In brief
The goal of this observational study is to learn if emotional distress affects how well liver cancer treatment works in people receiving immunotherapy. Emotional distress means feeling anxious or depressed. The study aims to answer whether having emotional distress before treatment or changes in emotional distress during treatment affect how well immunotherapy works to treat liver cancer. Researchers will compare participants with and without emotional distress to examine differences in how long the cancer stays under control, treatment response, and overall survival time. Study participants will complete mood and quality of life questionnaires, meet with mental health specialists for emotional assessments, undergo regular blood tests to measure stress hormones, have routine medical check-ups and scans to monitor their cancer status, and be followed for up to 3 years. The study includes three groups of people with liver cancer: those starting immunotherapy for cancer that cannot be removed by surgery, those receiving immunotherapy after surgery, and those receiving immunotherapy before surgery. To be eligible for participation, individuals must be 18 years or older, diagnosed with liver cancer, about to start immunotherapy treatment, and able to complete mood questionnaires.
Key facts
- Study ID
- NCT07141056
- Run by
- Guilin Medical University, China
- People needed
- 700
- Starts
- 2025-01-01
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2025-08-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years
- Able to complete psychological questionnaires
- Child-Pugh liver function class A
- ECOG performance status ≤ 1
- Signed informed consent
- Expected survival > 3 months
- Diagnosed with unresectable HCC by pathology or imaging
- BCLC stage B or C
- Has at least one measurable lesion (mRECIST)
- About to receive first-line ICI treatment
You may not qualify if…
- Currently taking antidepressant or anti-anxiety medications
- Previous diagnosis of psychiatric disorders
- Concurrent malignancy
- Unable to complete psychological assessments
- Previous systemic anti-tumor therapy
- Symptomatic brain metastases
- Child-Pugh score > 7
- Cohort 2 (SOLACE-2):
- Inclusion Criteria:
- Age ≥ 18 years
- Able to complete psychological questionnaires
- Child-Pugh liver function class A
- ECOG performance status ≤ 1
- Signed informed consent
- Expected survival > 3 months
- Pathologically confirmed HCC after curative surgery
- Pathological stage II or III (AJCC 8th edition)
- Will start adjuvant ICI therapy within 4-6 weeks after surgery
- Expected survival > 12 months
- Exclusion Criteria:
- Currently taking antidepressant or anti-anxiety medications
- Previous diagnosis of psychiatric disorders
- Concurrent malignancy
- Unable to complete psychological assessments
- Residual lesions after surgery
Where it is running
- The Second Affiliated Hospital of Guangdong Medical University — Zhanjiang, Guangdong, China (enrolling)
- The Affiliated Hospital of Guilin Medical University — Guilin, Guangxi, China (enrolling)
- The Second Affiliated Hospital of Guilin Medical University — Guilin, Guangxi, China (enrolling)
- Shaoyang Central Hospital — Shaoyang, Hunan, China (enrolling)
- The First Affiliated Hospital of Shaoyang College — Shaoyang, Hunan, China (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.