@article{d6cadd3ec74f451383bdadb394c6bf06,
title = "Immunotherapy Use in Patients with Lung Cancer and Comorbidities",
abstract = "Immune checkpoint inhibitor (ICI) therapy is now in widespread clinical use for the treatment of lung cancer. Although patients with autoimmune disease and other comorbidities were excluded from initial clinical trials, emerging real-world experience suggests that these promising treatments may be administered safely to individuals with inactive low-risk autoimmune disease such as rheumatoid arthritis or psoriasis, mild to moderate renal and hepatic dysfunction, and certain chronic viral infections. Considerations for ICI in autoimmune disease populations include exacerbations of the underlying autoimmune disease, increased risk of ICI-induced immune-related adverse events, and potential for compromised efficacy if patients are receiving chronic immunosuppression. Immune checkpoint inhibitor use in higher-risk autoimmune conditions, such as myasthenia gravis or multiple sclerosis, requires careful evaluation on a case-by-case basis. Immune checkpoint inhibitor use in individuals with solid organ transplant carries a substantial risk of organ rejection. Ongoing research into the prediction of ICI efficacy and toxicity may help in patient selection, treatment, and monitoring.",
keywords = "Autoimmune disease, immune checkpoint inhibitors, immune-related adverse events, immunosuppression, transplant",
author = "{Von Itzstein}, {Mitchell S.} and Gonugunta, {Amrit S.} and Mayo, {Helen G.} and Minna, {John D.} and Gerber, {David E.}",
note = "Funding Information: From the *Department of Medicine, Division of Hematology and Oncology, University of Texas, Southwestern Medical Center; †Hamon Center for Therapeutic Oncology Research and the Simmons Comprehensive Cancer Center, UT Southwestern Medical Center; ‡UT Southwestern Medical School; §UT Southwestern Health Sciences Digital Library and Learning Center; and ||Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX. Conflicts of Interest and Source of Funding: Funded in part by a National Cancer Institute Midcareer Investigator Award in Patient-Oriented Research (K24 CA201543-01), the National Institute of Allergy and Infectious Disease (1U01AI156189-01), an American Cancer Society-Melanoma Research Alliance Team Award (MRAT-18-114-01-LIB), a V Foundation Robin Roberts Cancer Survivorship Award (DT2019-007), the University of Texas Lung Cancer Specialized Program in Research Excellence (SPORE, P50-CA-070907-08S1), and The University of Texas Southwestern Medical Center–Dallas holds a Physician-Scientist Institutional Award from the Burroughs Wellcome Fund. The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article. Reprints: David E. Gerber, MD, Division of Hematology-Oncology, Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Mail Code 8852, Dallas, TX 75390. E‐mail: david.gerber@utsouthwestern.edu. Supplemental digital contents are available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal{\textquoteright}s Web site (www.journalppo.com). Copyright {\textcopyright} 2020 Wolters Kluwer Health, Inc. All rights reserved. ISSN: 1528-9117 Publisher Copyright: {\textcopyright} Wolters Kluwer Health, Inc. All rights reserved.",
year = "2020",
month = nov,
doi = "10.1097/PPO.0000000000000484",
language = "English (US)",
volume = "26",
pages = "525--536",
journal = "Cancer Journal",
issn = "1528-9117",
number = "6",
}