COPD and Immune Checkpoint Inhibitors for Cancer: A Literature Review

被引:0
作者
Jr, Thomas W. Lycan [1 ,2 ]
Norton, Dustin L. [1 ]
Ohar, Jill A. [1 ]
机构
[1] Wake Forest Univ, Sch Med, Dept Internal Med, Sch Med, Winston Salem, NC 27101 USA
[2] Wake Forest Univ, Sch Med, Wake Forest Inst Regenerat Med, Med Ctr Blvd, Winston Salem, NC 27157 USA
来源
INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE | 2024年 / 19卷
基金
美国国家卫生研究院;
关键词
lung cancer; COPD; immunotherapy; immune checkpoint inhibitors; OBSTRUCTIVE PULMONARY-DISEASE; CELL LUNG-CANCER; T-CELLS; EFFICACY; PNEUMONITIS; IMMUNOTHERAPY; ABNORMALITIES; RADIOTHERAPY; DYSFUNCTION; ASSOCIATION;
D O I
10.2147/COPD.S490252
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose: Immune checkpoint inhibitors are a standard treatment option for many patients with cancer and are most frequently used to treat lung cancer. Chronic obstructive pulmonary disease (COPD) is the most common comorbidity of patients with lung cancer. As the cancer-specific survival of patients with lung cancer continues to increase with modern treatments, it is critical to optimize comorbidities to improve overall survival. This literature review aimed to summarize current research on the impact of COPD upon immunotherapy outcomes. Methods: A comprehensive search was conducted in the PubMed database using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Inclusion criteria focused on peer-reviewed articles published between 2010 and 2024 that addressed COPD, cancer, and immune checkpoint inhibitors. The study team screened the studies for relevance and then synthesized them narratively. Results: This review identified 37 studies that met the inclusion criteria. Findings suggest that COPD is predictive of improved efficacy but slightly worse toxicity from immune checkpoint inhibitor therapy. The chronic inflammation of COPD leads to immune exhaustion including the overexpression of immune checkpoints on T-cells. Particularly within "hot" tumors that have higher concentrations of tumor-infiltrating lymphocytes, the COPD-related increase in programmed cell death protein 1 (PD-1) signaling likely creates sensitivity to immune checkpoint inhibitors. However, COPD can also lead to respiratory dysfunction, debility, and interstitial lung disease; each of which increases the severity of immune-related adverse events. Conclusion: COPD is a critical comorbidity that has a significant impact on many patients with cancer who receive treatment with immune checkpoint inhibitors. Future research is needed to design interventions to optimize COPD care in this high-risk patient population.
引用
收藏
页码:2689 / 2703
页数:15
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