AI Article Synopsis

  • The study focused on how the management of immune-related adverse events (irAEs) from checkpoint inhibitors has changed over time at a cancer care center.
  • It found that while there were improvements in management of pulmonary irAEs in 2021, gastrointestinal irAEs saw a decline in follow-up and treatment efforts.
  • The research highlights the need for timely specialty consultations, particularly for gastrointestinal irAEs, to enhance patient outcomes and suggests that findings can inform better management strategies at various institutions.

Article Abstract

Understanding of immune-related adverse events (irAEs) has evolved rapidly, and management guidelines are continually updated. We explored temporal changes in checkpoint inhibitor-induced irAE management at a tertiary cancer care center to identify areas for improvement. We conducted a single-center retrospective study of patients who developed a gastrointestinal, pulmonary, renal, or cardiac irAE between July and 1 October in 2019 or 2021. We collected patient demographic and clinical information up to 1 year after toxicity. Endoscopic evaluation and specialty follow-up after discharge for patients with gastrointestinal irAEs declined between the 2019 and 2021 periods. Symptom duration and steroid taper attempts also declined. For pulmonary irAEs, rates of specialty consultation, hospital admission and readmission, and mortality improved in 2021 compared with 2019. Follow-up rates after hospital discharge were consistently low (<50%) in both periods. For cardiac irAEs, consultation with a cardiologist was frequent and prompt in both periods. Outpatient treatment and earlier specialty consultation improved outcomes with gastrointestinal irAEs. Our study exploring irAE practice changes over time identified areas to improve management; specifically, timely specialty consultation was associated with better outcomes for gastrointestinal irAEs. These findings can help improve the quality of management algorithms at our institution and may inform policies in other institutions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10814014PMC
http://dx.doi.org/10.3390/cancers16020369DOI Listing

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