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Impact of Emotional Stress on Immune Checkpoint Inhibitor Treatment Outcomes in Hepatocellular Carcinoma: A Multicohort Clinical Study

Impact of Emotional Stress on Immune Checkpoint Inhibitor Treatment Outcomes in Hepatocellular Carcinoma: A Multicohort Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094830
Enrollment
Unknown
Registered
2024-12-27
Start date
2024-12-31
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Hepatocellular Carcinoma

Interventions

Sponsors

Affiliated Hospital of Guilin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Cohort 1: Age>=18 years; Confirmed diagnosis of unresectable HCC by pathology or imaging; BCLC stage B or C; Child-Pugh score of liver function grade A or B ( 3 months; Signed informed consent. Cohort 2: Age>=18 years; Confirmed diagnosis of HCC by pathology and radical surgical resection; The postoperative pathological stage was stage II or III (AJCC version 8); Child-Pugh score of liver function: grade A; Adjuvant ICI therapy will be started within 4-6 weeks after surgery; ECOG performance status score12 months; Signed informed consent. Cohort 3: Age>=18 years; Diagnosed with HCC by pathology or imaging, assessed as resectable; The clinical stage is stage II or III (AJCC version 8); Child-Pugh score of liver function: grade A; Upcoming neoadjuvant ICI therapy; ECOG performance status score 12 months; Signed informed consent.

Exclusion criteria

Exclusion criteria: Cohort 1: Prior systemic anti-tumor therapy; concurrent malignancy; severe cardiac, pulmonary, or renal dysfunction; current use of antidepressants or anxiolytics; history of psychiatric disorders; symptomatic brain metastases; unable to complete psychological assessment scales. Cohort 2: Residual lesions after surgery; concurrent malignancy; severe cardiac, pulmonary, or renal dysfunction; current use of antidepressants or anxiolytics; history of psychiatric disorders; unable to complete psychological assessment scales. Cohort 3: Prior systemic anti-tumor therapy; concurrent malignancy; severe cardiac, pulmonary, or renal dysfunction; current use of antidepressants or anxiolytics; history of psychiatric disorders; symptomatic brain metastases; unable to complete psychological assessment scales.

Design outcomes

Primary

MeasureTime frame
Serum Cortisol;Plasma Adrenocorticotropic Hormone;Patient Health Questionnaire-9;Generalized Anxiety Disorder-7 Scale;European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (Version 3);

Countries

China

Contacts

Public ContactYu Yaqun

The Affiliated Hospital of Guilin Medical University

yelinohi@163.com+86 158 0773 9295

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026