This narrative review evaluates the role of immune checkpoint inhibitors (ICIs), specifically PD-1/PD-L1 and CTLA-4 inhibitors, in the treatment of patients with lung cancer, including non-small cell and small cell types. The scope encompasses ICIs administered as monotherapy or in combination with chemotherapy, radiotherapy, and anti-angiogenic agents within a clinical practice setting. The review addresses therapeutic heterogeneity across histological types and response patterns in specific patient subgroups.
The authors synthesize key findings regarding survival benefits and the mechanisms of primary and acquired resistance. Resistance is attributed to tumor microenvironment immunosuppression, impaired antigen presentation, and aberrant signaling. The review also details immune-related adverse events (irAEs) occurring across multiple organ systems and notes that treatment discontinuation occurs occasionally.
Significant limitations are identified, particularly concerning existing biomarkers like PD-L1 expression and tumor mutational burden. The authors point to insufficient standardization and spatiotemporal heterogeneity as barriers to effective biomarker utilization. Consequently, the review underscores the necessity of personalized immunotherapy approaches to address these challenges.
Practice relevance is framed around the need for tailored treatment strategies. The authors caution against overreliance on current biomarkers due to their inherent limitations. Overall, the review provides a qualitative overview of the landscape of immunotherapy in lung cancer without reporting specific numerical outcomes or sample sizes.
View Original Abstract ↓
Lung cancer remains a leading cause of global cancer-related mortality, with most patients diagnosed at advanced stages. The emergence of immune checkpoint inhibitors (ICIs), specifically targeting PD-1/PD-L1 and CTLA-4 pathways, has revolutionized the treatment landscape by restoring anti-tumor immune responses. Currently, ICIs are integrated into clinical practice across all stages of lung cancer, administered either as monotherapy or in combination with chemotherapy, radiotherapy, and anti-angiogenic agents. Despite significant survival benefits, several critical challenges persist. First, primary and acquired resistance, driven by tumor microenvironment (TME) immunosuppression, impaired antigen presentation, and aberrant signaling, limits long-term efficacy. Second, existing biomarkers like PD-L1 expression and tumor mutational burden (TMB) face limitations due to insufficient standardization and spatiotemporal heterogeneity. Furthermore, immune-related adverse events (irAEs) across multiple organ systems necessitate vigilant clinical management and occasionally treatment discontinuation. This review systematically evaluates the research progress and clinical applications of ICI therapy in lung cancer. We highlight the therapeutic heterogeneity observed across different histological types, including non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC), with a specific focus on the management of brain metastases (BMs). Additionally, the article discusses varying response patterns within specific patient subgroups, such as geriatric patients and individuals with differing smoking or performance statuses. By synthesizing data on both favorable therapeutic outcomes and the spectrum of irAEs, we emphasize the necessity of personalized immunotherapy. Ultimately, this review looks forward to future advancements aimed at enhancing the precision and safety of lung cancer treatment, providing a roadmap for more tailored clinical interventions.