Association between pretreatment emotional distress and immune checkpoint inhibitor response in non-small-cell lung cancer

Связь эмоционального дистресса до начала лечения с ответом на ингибиторы иммунных контрольных точек при немелкоклеточном раке лёгкого
Yue Zeng, Chunhong Hu, Yizheng Li, Jiansong Zhou, Shuxing Wang, Mengdong Liu, Zhenhua Qiu, Chao Deng, Fang Ma, Chun‐Fang Xia, Fei Liang, Yurong Peng, Ao-Xi Liang, Sheng-Hao Shi, Shi-Jiao Yao, Junqi Liu, Wenjie Xiao, Xiao-Qiao Lin, Xinyu Tian, Ying-Zhe Zhang, Z. Tian, Ji-An Zou, Yun-Shu Li, Chao-Yue Xiao, Xu Tian, Xiaojie Zhang, Xiaoping Wang, Xianling Liu, Fang Wu
2024-05-13

blood cortisol levelsemotional distressimmune checkpoint inhibitorsnon-small-cell lung cancerprogression-free survival
Emotional distress (ED), commonly characterized by symptoms of depression and/or anxiety, is prevalent in patients with cancer. Preclinical studies suggest that ED can impair antitumor immune responses, but few clinical studies have explored its relationship with response to immune checkpoint inhibitors (ICIs). Here we report results from cohort 1 of the prospective observational STRESS-LUNG study, which investigated the association between ED and clinical efficacy of first-line treatment of ICIs in patients with advanced non-small-cell lung cancer. ED was assessed by Patient Health Questionnaire-9 and Generalized Anxiety Disorder 7-item scale. The study included 227 patients with 111 (48.9%) exhibiting ED who presented depression (Patient Health Questionnaire-9 score ≥5) and/or anxiety (Generalized Anxiety Disorder 7-item score ≥5) symptoms at baseline. On the primary endpoint analysis, patients with baseline ED exhibited a significantly shorter median progression-free survival compared with those without ED (7.9 months versus 15.5 months, hazard ratio 1.73, 95% confidence interval 1.23 to 2.43, P = 0.002). On the secondary endpoint analysis, ED was associated with lower objective response rate (46.8% versus 62.1%, odds ratio 0.54, P = 0.022), reduced 2-year overall survival rate of 46.5% versus 64.9% (hazard ratio for death 1.82, 95% confidence interval 1.12 to 2.97, P = 0.016) and detriments in quality of life. The exploratory analysis indicated that the ED group showed elevated blood cortisol levels, which was associated with adverse survival outcomes. This study suggests that there is an association between ED and worse clinical outcomes in patients with advanced non-small-cell lung cancer treated with ICIs, highlighting the potential significance of addressing ED in cancer management. ClinicalTrials.gov registration: NCT05477979 .
1
Baseline emotional distress was associated with significantly shorter progression-free survival under first-line immune checkpoint inhibitors: 7.9 versus 15.5 months (HR 1.73, P = 0.002).
2
Emotional distress was associated with worse overall survival, including 2-year survival of 46.5% versus 64.9% (HR for death 1.82, P = 0.016), and poorer quality of life.
3
In the prospective STRESS-LUNG cohort, 48.9% of 227 patients with advanced NSCLC had baseline emotional distress involving depression and/or anxiety symptoms.
4
Patients with emotional distress had a lower objective response rate than those without distress: 46.8% versus 62.1% (OR 0.54, P = 0.022).
5
The emotional-distress group had elevated blood cortisol levels, which were associated with adverse survival outcomes, suggesting cortisol as a potential correlate of poorer ICI outcomes.

Patients with advanced non-small-cell lung cancer treated with first-line immune checkpoint inhibitors

The association of pretreatment emotional distress with immune checkpoint inhibitor efficacy, survival outcomes, quality of life, and blood cortisol levels

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2024-05-13
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Authors
Yue Zeng
Chunhong Hu
Yizheng Li
Jiansong Zhou
Shuxing Wang
Mengdong Liu
Zhenhua Qiu
Chao Deng
Fang Ma
Chun‐Fang Xia
Fei Liang
Yurong Peng
Ao-Xi Liang
Sheng-Hao Shi
Shi-Jiao Yao
Junqi Liu
Wenjie Xiao
Xiao-Qiao Lin
Xinyu Tian
Ying-Zhe Zhang
Z. Tian
Ji-An Zou
Yun-Shu Li
Chao-Yue Xiao
Xu Tian
Xiaojie Zhang
Xiaoping Wang
Xianling Liu
Fang Wu
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