Age-Associated Changes in Adverse Events Arising From Anti-PD-(L)1 Therapy

Background Immune-related adverse events (irAEs) may complicate the immune checkpoint inhibition (ICI) therapy. The effect of age on these irAEs is not elucidated. The aim of the study was to compare the occurrence of irAEs in different age groups. Methods Patients with lung cancer receiving anti-programmed death- (ligand)1 (PD-(L)1) were selected from the US Food and Drug Administration Adverse Event Reporting System (FAERS) database. Immune cell infiltration data set was obtained from TIMER 2.0 web server. The patients were stratified for age as follows: <65 year-old (young patients, YP), 65 to 75 year-old (middle aged patients, MP), >= 75 year-old (old patients, OP). The severity of irAEs was compared using logistic binary regression model. The distribution differences of immune cell infiltration were estimated using non-parametric tests. Results Of all the 17,006 patients treated by anti-PD-(L)1, 7,355 were <65 (YP), 6,706 were 65-75 (MP), and 2,945 were >= 75 (OP). In general, we analyzed a total of 16 irAEs in this article and found that pulmonary toxicity was more frequent in OP (OP vs. YP: OR = 1.45, 95% CI: 1.28-1.64) and MP (MP vs. YP: OR = 1.38, 95% CI: 1.24-1.52), but hepatitis was less frequent in OP (OP vs. YP: OR = 0.56, 95% CI: 0.32-0.97) and MP (MP vs. YP: OR = 0.57, 95%CI: 0.38-0.85). Further analysis demonstrated that older patients showed less B cell, CD8(+) T cell and myeloid dendritic cell infiltration than younger patients. Conclusions Elderly patients exhibited higher incidences of pulmonary toxicity, while hepatitis was found at low incidence. Therefore, clinicians should carefully monitor comorbidities in elderly patients.

Automated summary

This study compared the occurrence of immune-related adverse events (irAEs) in different age groups receiving immune checkpoint inhibition therapy. It was found that older patients had higher incidences of pulmonary toxicity and lower rates of hepatitis compared to younger patients. Additionally, older patients showed decreased infiltration of B cells, CD8(+) T cells, and myeloid dendritic cells.