442 Pre-treatment interstitial abnormalities is a risk factor for immune checkpoint inhibitor pneumonitis in patients with lung cancer

Background

Immune checkpoint inhibitors (ICIs) are a first line and adjuvant treatment in advanced stage lung cancer. One of the main complications of ICI treatment is pneumonitis with an overall incidence of 2-5%; however, patient specific risk factors for developing ICI-pneumonitis (ICI-p) haven’t been well elucidated. ^1,2 We evaluated potential pre-treatment risk factors for ICI-p including pre-treatment interstitial abnormalities on computed tomography of the chest (CT chest).

Methods

We conducted a retrospective cohort study of consecutive patients with lung cancer who received at least one dose of ICI between 2015-2020 at The Ohio State University. Potential risk factors for ICI-p were recorded and summarized between those with and without pneumonitis. Among patients who developed pneumonitis, these factors were compared between Grade <3 and Grade >=3 severities as well as among patients with different cancer stage (3 vs 4). Multivariable survival analysis was used to examine the association of potential risk factors with pneumonitis. Pneumonitis cases were documented by the treating oncologist and retrospectively evaluated by an oncologist and pulmonologist.

Results

473 patients with lung cancer were included, 401 with Non-Small Cell Lung Cancer and 72 with Small Cell Lung Cancer. 38 developed ICI-p and 435 did not. Of the potential risk factors, the following were significantly associated with ICI-p: pre-existing interstitial abnormalities (30.8% vs 4.2%, p < 0.001), prior concurrent chemoradiation (17.7% vs 4.2%, p <0.001), stage of cancer (19.8% for stage III vs 4.4% for stage IV, p < 0.001),), and type of immunotherapy (12.5% for PD1 vs 3.6% for chemo-IO, p < 0.001) (table 1). Pre-existing interstitial abnormalities remained strongly correlated with development of pneumonitis on multivariable analysis including prior chemoradiation, pre-treatment interstitial abnormalities, and type of immunotherapy, (hazard ratio 8.54 [4.45-16.42], p<0.001) (table 2). Interstitial abnormalities also remained significant in subgroup analysis of both stage 3 and 4 lung cancer (p<0.001). Patients with grade 3/4 pneumonitis had decreased overall survival compared to those with grade 1/2 pneumonitis (p = 0.0342) (figure 1).

Conclusions

Pre-existing interstitial abnormalities on CT chest is strongly associated with development of ICI-p in patients with lung cancer. It remains an independent risk factor after accounting for common treatment-related risk factors such as prior chemoradiation and chest radiation. Pre-treatment interstitial abnormalities could be utilized as a risk stratification tool to identify patients at highest risk for developing ICI-p, a devastating complication associated with higher mortality in more severe cases.

Acknowledgements

This study was supported by the National Institutes of Health (P30CA016058 and K12 CA133250). Research support provided by the REDCap project and The Ohio State University Center for Clinical and Translational Science grant support (National Center for Advancing Translational Sciences, Grant UL1TR002733)

References

Nishino M, Giobbie-Hurder A, Hatabu H, Ramaiya NH, Hodi FS. Incidence of Programmed Cell Death 1 Inhibitor-Related Pneumonitis in Patients With Advanced Cancer A Systematic Review and Meta-analysis. JAMA Oncology.2(12):1607–1616. Wu J, Hong D, Zhang X, Lu X, Miao J. PD-1 inhibitors increase the incidence and risk of pneumonitis in cancer patients in a dose-independent manner: a meta-analysis. Scientific Reports.7(1).

Ethics Approval

Human data was utilized in this project; CIRB approval was obtained and all participants provided informed consent prior to taking part in the study (Study number 2021C0069).