Expression of IL-4 in Tumors: A Safety Surrogate to Predict Cancer Survival Associated With Biologic Therapies

April 2024 | Volume 23 | Issue 4 | e118 | Copyright © April 2024


Published online March 27, 2024

Nikolai Klebanov MD*, Carly Grant MD*, Jeffrey S. Smith MD PhD, Lourdes M. Perez-Chada MD MMSc, Joseph F Merola MD MMSc

Department of Dermatology, Harvard Medical School, Brigham and Women’s Hospital, Boston, MA 
*Co-first author
 

Abstract

INTRODUCTION

Interleukin (IL)-4-targeted therapies have revolutionized management of inflammatory dermatoses. Dupilumab, an IL-4 receptor alpha inhibitor, is approved for moderate-to-severe atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyposis, and eosinophilic esophagitis1 with ongoing studies including in urticaria, prurigo nodularis, and alopecia.2 Interleukins are critical mediators of immunosurveillance, and a theoretical increased risk of malignancy exists for any interleukin inhibitor until real-world long-term safety data are explored. Genomic expression studies can help examine if interleukin deficiencies are associated with increased malignancy risk, providing a proxy for long-term interleukin repression.
 
We utilize data from the Cancer Genome Atlas to investigate if IL-4 expression is correlated with overall survival (OS) in