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NCT Number: NCT07141056

The Impact of Emotional Stress on Immunotherapy Outcomes in Liver Cancer Patients: A Multi-Cohort Study

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The Second Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China

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About this study

This multi-center prospective cohort study investigates the relationship between emotional distress (ED) and treatment outcomes in patients receiving immune checkpoint inhibitor (ICI) therapy for hepatocellular carcinoma (liver cancer). Recent research suggests that emotional distress may influence how well cancer treatments work, particularly immunotherapy, but this connection hasn't been well studied in liver cancer patients.

Scientific Background: Liver cancer is a major global health concern, with increasing cases worldwide. While immunotherapy has emerged as a promising treatment option, not all patients respond equally well to this therapy. Understanding factors that might influence treatment success is crucial for improving patient care. Recent studies have shown that emotional distress can affect immune system function, which may impact how well immunotherapy works.

Study Design: The study includes three distinct cohorts of liver cancer patients:

Cohort 1: Patients with unresectable liver cancer starting first-line ICI therapy Cohort 2: Patients receiving ICI therapy after surgery (adjuvant therapy) Cohort 3: Patients receiving ICI therapy before surgery (neoadjuvant therapy)

Comprehensive Assessment Approach:

Emotional distress will be evaluated through multiple methods:

Self-reported questionnaires (PHQ-9 for depression and GAD-7 for anxiety) Professional clinical assessments (Hamilton Depression Scale, Hamilton Anxiety Scale, and Clinical Global Impression Scale) Quality of life measurements Biological markers of stress measured through blood tests

Treatment Monitoring: Participants will receive standard-of-care immunotherapy according to their treating physician's recommendations. The study will not influence treatment decisions but will carefully monitor:

Treatment response through regular imaging Side effects Quality of life Changes in emotional well-being Biological markers of stress and immune function Expected Outcomes and Impact: This study aims to: Determine if emotional distress affects treatment outcomes, Identify which patients might benefit from additional psychological support Understand the biological mechanisms linking stress and treatment response, Develop better strategies for supporting patients during immunotherapy Patient Safety and Support: While this is an observational study that doesn't change standard treatment, we recognize that discussing emotional health can be sensitive. The study includes: Regular monitoring of participants' emotional well-being, Access to mental health professionals if needed, Clear protocols for handling any psychological concerns that arise, Protection of patient privacy and confidentiality Long-term Goals: The findings from this study could lead to: Better ways to identify patients who might need extra support during treatment, New strategies to improve treatment effectiveness, More personalized approaches to cancer care that consider both physical and emotional health, Improved understanding of how psychological factors affect cancer treatment Duration and Follow-up: The study will enroll participants over three years, with each participant followed for up to three years. This allows us to understand both immediate and long-term relationships between emotional well-being and treatment outcomes.

Study Innovation: This is one of the first large-scale studies to: Examine the impact of emotional distress on immunotherapy outcomes in liver cancer, Use both patient self-assessments and professional clinical evaluations, Study this relationship across different stages of treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Cohort 1 (SOLACE-1):

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
  • 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

Exclusion criteria

  • 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
  • Child-Pugh score B or C

Cohort 3 (SOLACE-3):

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
  • Diagnosed with resectable HCC by pathology or imaging
  • Has at least one measurable lesion (RECIST 1.1)
  • About to receive neoadjuvant ICI treatment
  • Expected survival > 12 months

Exclusion criteria

  • Currently taking antidepressant or anti-anxiety medications
  • Previous diagnosis of psychiatric disorders
  • Severe cardiac, pulmonary, or renal dysfunction
  • Concurrent malignancy
  • Unable to complete psychological assessments
  • Previous systemic anti-tumor therapy
  • Symptomatic brain metastases
  • Child-Pugh score B or C

Treatment and study plan

psychological stress status

Other

Psychological stress status will be assessed using both self-reported and clinician-rated measures. Participants will be categorized into stressed and non-stressed groups based on the following criteria: Self-reported measures (either): PHQ-9 score ≥ 5 (depression symptoms) and/or; GAD-7 score ≥ 5 (anxiety symptoms) Clinician-rated measures (either): HAMD score ≥ 7 (mild depression) and/or HAMA score ≥ 7 (mild anxiety) Additional assessments: Clinical Global Impression Scale (CGI) EORTC QLQ-C30 (quality of life) Assessment timing: Baseline (before starting immunotherapy) After 2-3 cycles of treatment Every 3 months during follow-up.

Primary outcomes

  1. Progression-Free Survival (PFS)

    Time frame: Up to 24 months

    Time from treatment initiation to disease progression or death

  2. Disease-Free Survival (DFS)

    Time frame: Up to 36 months

    Time from surgery to disease recurrence or death

  3. Pathological Complete Response (pCR) Rate

    Time frame: At time of surgery (approximately 6-8 weeks after neoadjuvant therapy)

    Percentage of participants achieving complete pathological response

Secondary outcomes

  1. Overall Survival (OS)

    Time frame: Up to 36 months

    Time from treatment initiation to death from any cause

  2. Objective Response Rate (ORR)

    Time frame: Up to 2 years (assessed every 6-8 weeks from from treatment initiation until disease progression or death from any cause)

    Percentage of participants achieving complete or partial response

  3. Stress Biomarker Levels

    Time frame: From baseline up to 36 months (assessed every 3 months until study completion, disease progression, or death from any cause, whichever occurs first)

    Changes in cortisol and ACTH levels

  4. Safety and Adverse Events

    Time frame: Throughout study duration (up to 36 months)

    Frequency and severity of adverse events

  5. Health-Related Quality of Life measured by EORTC QLQ-C30 Total Score

    Time frame: Baseline, 6 weeks, 9 weeks, then every 12 weeks through study completion (up to 3 years).

    EORTC QLQ-C30 (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-C30) scores. The scale ranges from 0 to 100, where higher scores represent better quality of life for functional scales and global health status, but higher scores represent worse symptoms for symptom scales.

  6. Changes in Depression Scores (PHQ-9)

    Time frame: Baseline, 6 weeks, 9 weeks, then every 12 weeks through study completion (up to 3 years)

    Changes in Patient Health Questionnaire-9 (PHQ-9) depression scores from baseline

  7. Changes in Anxiety Scores (GAD-7)

    Time frame: Baseline, 6 weeks, 9 weeks, then every 12 weeks through study completion (up to 3 years)

    Changes in Generalized Anxiety Disorder-7 (GAD-7) scores from baseline

  8. Changes in Depression Scores (HAMD)

    Time frame: Baseline, 6 weeks, 9 weeks, then every 12 weeks through study completion (up to 3 years)

    Changes in Hamilton Depression Rating Scale (HAMD) scores from baseline

  9. Changes in Anxiety Scores (HAMA)

    Time frame: Baseline, 6 weeks, 9 weeks, then every 12 weeks through study completion (up to 3 years)

    Changes in Hamilton Anxiety Rating Scale (HAMA) scores from baseline

Other outcomes

  1. Association between stress biomarkers and treatment response

    Time frame: Baseline, every 3 months during treatment, and up to 3 years follow-up

    Correlation between stress hormone levels and treatment outcomes

Study contacts

Contact information is provided by the study sponsor or research team.

Yu Yaqun, MD. PhD

CONTACT

[email protected]

+ 86 18172681387

Sponsors and collaborators

Lead sponsor

Guilin Medical University, China

Other

Registry information

Official study title

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

Acronym: SOLACE

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Aug 26, 2025
Registry last updated
Aug 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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