Publications by authors named "Jamie DiCarlo"

Background And Aims: Typical immune checkpoint inhibitor-induced colitis (T-ICI) has significant histomorphologic overlap with inflammatory bowel disease (IBD), a distinction further complicated in ICI-treated patients with pre-existing inflammatory bowel disease (P-IBD) and those with potentially "unmasked" inflammatory bowel disease (U-IBD) after ICI therapy. This study describes histopathologic findings seen in U-IBD colonic biopsies and assesses for distinguishing features from T-ICI and P-IBD biopsies.

Methods: Initial colon biopsies after symptom onset from 34 patients on ICI therapy were reviewed, and histopathologic features were tabulated.

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Introduction: Immune-related adverse events (irAE) secondary to immune checkpoint inhibitors (ICI) have gastrointestinal (GI) manifestations, including gastritis, enteritis, and/or colitis. The long-term sequelae of ICI-associated GI toxicities (GI-irAE), particularly the development of disorders of gut-brain interaction, are not well known. We characterized the incidence of persistent GI symptoms after GI-irAE.

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Synopsis of recent research by authors named "Jamie DiCarlo"

  • - Jamie DiCarlo's recent research primarily focuses on the gastrointestinal effects of immune checkpoint inhibitor therapy, particularly the histopathologic distinctions between inflammatory bowel disease (IBD) and immune checkpoint inhibitor-induced colitis (T-ICI).
  • - In a study involving colon biopsies from patients after ICI therapy, DiCarlo identified specific histopathologic features that help differentiate "unmasked" inflammatory bowel disease (U-IBD) from pre-existing IBD and T-ICI cases.
  • - Another aspect of DiCarlo's research examines the long-term consequences of gastrointestinal immune-related adverse events (GI-irAE) in melanoma patients, highlighting the development of persistent gastrointestinal symptoms and disorders related to gut-brain interactions following treatment.