4.7 Article

Characteristics of Immune Checkpoint Inhibitor-Associated Gastritis: Report from a Major Tertiary Care Center

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ONCOLOGIST
Volume -, Issue -, Pages -

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OXFORD UNIV PRESS
DOI: 10.1093/oncolo/oyad031

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This article describes a case series of 25 patients who were diagnosed with gastritis following immune checkpoint inhibitor therapy. The most common malignancies were non-small cell lung cancer and melanoma. Symptoms included nausea, vomiting, abdominal pain, and melena. Endoscopic findings showed erythema, edema, and friability. Most patients received acid suppression treatment and methylprednisolone. Approximately 64% of patients had complete resolution of symptoms within two months, and 52% were able to resume immunotherapy.
Background Immune checkpoint inhibitors (ICIs) have increased our ability to treat an ever-expanding number of cancers. We describe a case series of 25 patients who were diagnosed with gastritis following ICI therapy. Materials and Methods This was a retrospective study involving 1712 patients treated for malignancy with immunotherapy at Cleveland Clinic from January 2011 to June 2019 (IRB 18-1225). We searched electronic medical records using ICD-10 codes for gastritis diagnosis confirmed on endoscopy and histology within 3 months of ICI therapy. Patients with upper gastrointestinal tract malignancy or documented Helicobacter pylori-associated gastritis were excluded. Results Twenty-five patients were found to meet the criteria for diagnosis of gastritis. Of these 25 patients, most common malignancies were non-small cell lung cancer (52%) and melanoma (24%). Median number of infusions preceding symptoms was 4 (1-30) and time to symptom onset 2 (0.5-12) weeks after last infusion. Symptoms experienced were nausea (80%), vomiting (52%), abdominal pain (72%), and melena (44%). Common endoscopic findings were erythema (88%), edema (52%), and friability (48%). The most common diagnosis of pathology was chronic active gastritis in 24% of patients. Ninety-six percent received acid suppression treatment and 36% of patients also received steroids with an initial median dose of prednisone 75 (20-80) mg. Within 2 months, 64% had documented complete resolution of symptoms and 52% were able to resume immunotherapy. Conclusion Patients presenting with nausea, vomiting, abdominal pain, or melena following immunotherapy should be assessed for gastritis and if other causes are excluded, may require treatment as consideration for complication of immunotherapy. This article describes a case series of 25 patients who were diagnosed with gastritis following immune checkpoint inhibitor therapy.

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