Pre-Existing Autoimmune Disease and Mortality in Patients Treated with Anti-PD-1 and Anti-PD-L1 Therapy.
Kimberly TangBruce C TiuGuihong WanShijia ZhangNga NguyenBonnie LeungAlexander GusevKerry L ReynoldsShawn G KwatraYevgeniy R SemenovPublished in: Journal of the National Cancer Institute (2022)
Although indications for immune checkpoint inhibitors (ICIs) have dramatically increased in the past decade, ICIs have been associated with autoinflammatory immune-related adverse events, which can resemble autoimmune diseases (ADs). Little is known about the impact of baseline AD on mortality in cancer patients treated with ICIs. Here, we identified 17 497 patients with preexisting autoimmune diagnoses prior to treatment with antiprogrammed cell death receptor-1 or antiprogrammed cell death ligand-1 therapy and 17 497 matched controls through the TriNetX Diamond network of more than 200 million patients across the United States and Europe. Using a Cox proportional hazards model, we found that patients with history of AD were not at higher risk of mortality than non-AD patients (hazard ratio [HR] = 1.03, 95% confidence interval [CI] = 1 to 1.07; P = .05). Additionally, history of Hashimoto disease (HR = 0.75, 95% CI = 0.62 to 0.90; P = .002) and vitiligo (HR = 0.52, 95% CI = 0.34 to 0.81; P = .003) were statistically significantly associated with decreased mortality. This suggests that underlying AD need not be a contraindication to inclusion in clinical trials and administration of ICI for treatment of cancer.
Keyphrases
- cell death
- end stage renal disease
- clinical trial
- ejection fraction
- cardiovascular events
- newly diagnosed
- chronic kidney disease
- papillary thyroid
- multiple sclerosis
- stem cells
- risk factors
- peritoneal dialysis
- cardiovascular disease
- type diabetes
- squamous cell
- cell proliferation
- signaling pathway
- patient reported outcomes
- cell cycle arrest
- coronary artery disease
- mesenchymal stem cells
- cell therapy
- replacement therapy
- patient reported
- study protocol