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临床试验/NCT06964503
NCT06964503尚未招募不适用

Impact of Psychological Stress on Treatment Response and Prognosis in Lung Cancer Patients

The First Affiliated Hospital of Guangzhou Medical University0 个研究点目标入组 600 人开始时间: 2025年5月30日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
600
主要终点
Early-Stage Surgical Cohort: Disease-free survival (DFS)

研究概览

简要总结

This study explores how psychological stress may influence the treatment response and long-term outcomes in patients with lung cancer. While advances in surgery, chemotherapy, immunotherapy, and targeted therapies have improved survival, emotional well-being remains an often-overlooked factor. We aim to investigate whether high levels of stress, anxiety, or depression at the time of diagnosis or during treatment are linked to poorer responses to therapy or shorter survival. By identifying these associations, the study hopes to highlight the importance of psychological care as part of comprehensive cancer treatment. The findings may inform future strategies to integrate mental health support into routine care for patients with both early-stage and advanced lung cancer.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • 未提供

排除标准

  • •Combined with other malignant tumors in the past 3 years; Concurrent acute or chronic psychiatric disorders; Current receiving anti-depressive or anti-anxiety therapy; Previous treatment with other clinical drug trials; Patients with symptomatic brain metastasis; Can't cooperate with psychological scale assessment;
  • •Inclusion Criteria (Early-Stage Surgical Cohort) Age ≥18 years; Pathologically diagnosed as non-small-cell lung cancer; Pathologically stage conformed as early stage of IA-IIIA Available for tumor tissue samples; Systematic treatments naive ( e. g., chemotherapy, anti-angiogenic drugs, targeted drugs, and immunotherapy ); Receiving radical surgery; Informed and agreed to participate in the study;
  • •Exclusion Criteria:
  • •Combined with other malignant tumors in the past 3 years; Concurrent acute or chronic psychiatric disorders; Current receiving anti-depressive or anti-anxiety therapy; Previous treatment with other clinical drug trials; Can't cooperate with psychological scale assessment;
  • •Inclusion Criteria (neoadjuvant therapy Cohort) Adults aged ≥18 years; Histologically confirmed diagnosis of non-small cell lung cancer [NSCLC]; Clinical stage IB-IIIB based on the 8th edition of the AJCC TNM staging system and deemed potentially resectable after neoadjuvant therapy; At least one measurable lesion can be evaluated according to the RECIST 1.1 standard; Planned to receive or currently receiving neoadjuvant systemic therapy (e.g., chemotherapy, targeted therapy, or immunotherapy) with curative intent; Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 prior to neoadjuvant treatment; No prior systemic treatment before the initiation of neoadjuvant therapy; Able to provide informed consent and voluntarily agree to participate in the study
  • •Exclusion Criteria:
  • •Combined with other malignant tumors in the past 3 years; Concurrent acute or chronic psychiatric disorders; Current receiving anti-depressive or anti-anxiety therapy; Previous treatment with other clinical drug trials; Can't cooperate with psychological scale assessment;

结局指标

主要结局

Early-Stage Surgical Cohort: Disease-free survival (DFS)

时间窗: 5 years

The duration between the date after surgery to the date of any recurrence or death firstly

Advanced Stage Cohort: Progression-free survival (PFS)

时间窗: 3 years

Time from the beginning of first-line immunotherapy to the first progression (PD) in patients with lung cancer

neoadjuvant therapy Cohort: Pathologic complete response (pCR) rate

时间窗: 3 years

pCR is no viable tumor cells in tumor bed and lymph nodes. The pCR rate is the proportion of patients with a pathologic complete response.

次要结局

  • Overall survival (OS)(5 years)
  • Objective Response Rate (ORR)(3 years)

研究者

发起方
The First Affiliated Hospital of Guangzhou Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jianxing He

PHD

The First Affiliated Hospital of Guangzhou Medical University

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