Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/21009
Title: Association of good oncological response to therapy with the development of rheumatic immune-related adverse events following PD-1 inhibitor therapy.
Authors: Liew, David F L;Leung, Jessica L Y;Liu, Bonnia;Cebon, Jonathan S;Frauman, Albert G;Buchanan, Russell R C
Affiliation: School of Cancer Medicine, La Trobe University, Melbourne, VIC, Australia
Department of Clinical Pharmacology and Therapeutics, Austin Health, Heidelberg, Victoria, Australia
Department of Medicine, University of Melbourne, Melbourne, VIC, Australia
Olivia Newton John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia
Department of Rheumatology, Austin Health, Heidelberg, Victoria, Australia
Issue Date: Feb-2019
EDate: 2018-11-22
Citation: International journal of rheumatic diseases 2019; 22(2): 297-302
Abstract: To investigate whether any patient or treatment characteristics are associated with the development of rheumatic immune-related adverse events (irAEs) following programmed cell death protein 1 (PD-1) inhibitor therapy for cancer. This was a retrospective chart review of all patients who were dispensed nivolumab or pembrolizumab at a single center before 1 January, 2017, with follow-up until 1 July, 2017. Patients with any diagnosis of a non-cutaneous irAE were identified, regardless of severity, and rheumatic irAEs were characterized. Of 244 episodes of therapy, a non-cutaneous irAE occurred in 72 (29.5%). Rheumatic irAEs were diagnosed in 19 episodes of therapy (7.8%), with 12 de novo diagnoses (5.1% of episodes without a pre-existing autoimmune rheumatic disease) and 7 exacerbations of existing disease. Review by a rheumatologist occurred in only 11 of these. Rheumatic irAEs were more common in patients with a good oncological response to therapy (relative risk [RR] 11.16), those being treated for melanoma (RR 2.94) and those who developed another non-cutaneous irAE (RR 2.64). Rheumatic irAEs are relatively common with PD-1 inhibitor therapy, and appear to be associated with a good oncological response to therapy. Many rheumatic irAEs were not referred to rheumatological services. Prospective systematic investigation would be of benefit to explore these characteristics.
URI: http://ahro.austin.org.au/austinjspui/handle/1/21009
DOI: 10.1111/1756-185X.13444
ORCID: 0000-0001-8451-8883
0000-0002-3898-950X
PubMed URL: 30549256
Type: Journal Article
Subjects: antineoplastic agents
arthritis
drug-related side effects and adverse reactions
immunological
programmed cell death 1 receptor
Appears in Collections:Journal articles

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