Temporal observation of endoscopic and histological findings of gastritis after administration of an immune checkpoint inhibitor: a case report

Immune checkpoint inhibitors (ICIs) are widely used in the treatment of various cancers, including gastric and esophageal cancers. ICIs are monoclonal antibodies that target negative immunomodulatory molecules, such as cytotoxic T-lymphocyte antigen 4 (CTLA-4) receptors, the programmed cell death 1 (PD-1) receptor, and the PD-1 ligand (PD-L1). Pembrolizumab is a PD-1 antibody that is an effective treatment for un-resectable advanced lung cancer [1]. The adverse effects of ICIs are known as immune-related adverse events (irAEs), and many reports on irAEs, such as colitis and hepatitis, have already been published. However, there have been few reports on gastritis, and the characteristics of endoscopic findings and changes over time have not been clearly elucidated. Herein, we present a case of gastritis that developed after the administration of pembrolizumab. We report the temporal changes in symptoms, affected sites, and endoscopic findings of gastritis after ICI administration through comparison with previous case reports.

A 71-year-old Japanese man with un-resectable advanced lung adenocarcinoma was started on a once-every-three-week regimen of 200 mg pembrolizumab, a PD-1 inhibitor, at the Department of Pulmonary Medicine in our hospital in 2019. At that time, the patient was 167 cm tall and weighed 63 kg. He had a history of pulmonary tuberculosis, chronic obstructive pulmonary disease, and hypertrophic cardiomyopathy. His only oral medication was bisoprolol fumarate for cardiac disease. He had no food or drug allergies and consumed approximately 20 g of alcohol and 15 cigarettes per day. After 19 cycles of treatment, the patient developed epigastric pain and underwent upper gastrointestinal endoscopy, which revealed multiple erosions in the gastric antrum. Antacid treatment was started, and the patient was followed up for approximately 20 weeks; however, after 27 courses of treatment, he became anorexic. Blood tests showed no elevation of white blood cells or a decrease in hemoglobin in the peripheral blood, and both renal and liver functions were normal. When endoscopy was performed again, the erosions observed in the previous examination had spread extensively from the gastric antrum to the gastric body, and the number of erosions had increased.

Endoscopic examination of the stomach revealed extensive erosions and erythema with solid white exudate from the gastric antrum to the greater curvature of the gastric body (Fig. 1). No abnormal findings were noted in the esophagus or duodenum. Tissue biopsy of the gastric erosion showed inflammatory cell infiltration into the interstitium, mainly lymphocytes and plasma cells, as well as thickening of the muscularis mucosae and granulation tissue (Fig. 2). Immunohistochemistry analysis revealed increased numbers of both CD4-positive T cells and CD8-positive T cells, but the increase in CD8-positive T cells was particularly dominant. Furthermore, there were no other findings that would raise suspicion of malignant diseases such as cancer or lymphoma.

Bild vergrößern

Bild vergrößern

The patient was treated for Helicobacter pylori infection 3 years ago before starting pembrolizumab therapy, and the blood test results for antibodies to H. pylori were negative. There was no history of non-steroidal anti-inflammatory drug use or radiation therapy. Unfortunately, we did not test the patient for Cytomegalovirus (CMV) antibody titer or measured the gastrin level in the blood. Based on the clinical course, we strongly suspected ICI-related drug-induced gastritis. Therefore, pembrolizumab was discontinued, and the patient’s gastrointestinal symptoms improved within 1 week after discontinuation. Endoscopic observation of the stomach was performed 2, 5, and 9 months after discontinuation of pembrolizumab, and improvement in gastric mucosal findings was confirmed. Furthermore, by performing mucosal biopsies at each endoscopic observation, we confirmed a decrease in the number of CD8-positive T cells and an increase in the CD4/CD8 ratio in the mucosa (Fig. 3). The gastrointestinal symptoms and mucosal findings improved only with the discontinuation of ICI and administration of antacids, so steroids were not used. The patient’s gastrointestinal symptoms have not recurred more than 1 year after the discontinuation of the treatment (Fig. 4). Although the primary lung lesion is slowly worsening, the patient is being monitored by the attending respiratory physician without additional anticancer therapy.

Bild vergrößern

Bild vergrößern

In cancer treatment with ICI, irAEs are a potential cause of concern for many patients and clinicians. In terms of their frequency, gastrointestinal toxicity has been found to be the second-most common irAE after dermal toxicity [2]. However, the exact frequency of gastritis caused by ICI is unknown because there have been only 17 reports to date, including the present case [3‐16].

Among these reported cases (including our report), the male-to-female ratio was 9:8, the median age was 68 years, and the median time of onset was 24 weeks (Table 1). The primary diseases were malignant melanoma in nine patients and lung cancer in seven patients. Nivolumab was used in eight patients and pembrolizumab in six patients. The condition of most patients improved with the use of steroids; however, as in the present case, some patients only recovered by discontinuing the ICI therapy. In the reports of steroid administration, most cases were treated with 1 mg/kg of prednisolone or methylprednisolone orally or intravenously. There were few specific descriptions of the duration of steroid administration, but all reports appeared to evaluate the effect of steroids within a short period and then taper off or terminate the treatment. In general, we believe that long-term administration of high-dose steroids is undesirable and should be promptly discontinued or tapered as symptoms and inflammation improved. If there is little improvement in the symptoms, the introduction of biologic agents such as infliximab should be considered. In our case, since the patient’s subjective symptoms were minimal and his general condition was good, we decided to discontinue drug administration and monitor his progress. If the symptoms did not improve, we would have considered administering steroids, such as prednisolone.

The prognosis of gastritis caused by ICI appears to be relatively good, with improvement in clinical symptoms in all case reports.

As in the present case, epigastric pain and anorexia were frequently reported in previous cases. Although not observed in our case, there were many reports of patients with gastritis, esophagitis, duodenitis, and terminal ileitis as irAEs. A stand-by colonoscopy was also performed in the present case, but no mucosal abnormalities were found in the terminal ileum to the colon.

As in our case, endoscopic findings of previous reports showed that inflammation was mainly located in the area from the gastric antrum to the gastric body. Although reports of mucosal findings varied, erythema and erosion were the most common findings, followed by edema and diffuse white exudation. These were also observed in the present case, and the diffuse white exudate appeared flashy and could be considered an impressive finding of gastritis after ICI administration.

Pathological findings of previous cases included cryptitis, atrophy, and destruction of glands, with lymphocytic and neutrophilic infiltrates being especially common (Table 2). Despite a few reports of immuno-histochemical staining for CD4, CD8, etc., increased numbers of CD8-positive and CD4-positive T cells have been reported. In gastritis caused by ICI, Irshaid et al. reported a significant decrease in the CD4/CD8 ratio compared with that of normal tissues [17]. Consistent with the previous reports, in the present case, the number of CD8-positive T cells predominantly increased during the period of severe inflammation. We also observed a significant decrease in the number of CD8-positive T cells and an increase in the CD4/CD8 ratio as mucosal inflammation improved.

However, we had not completely ruled out the influence of infection. The subjective symptoms in our case (temporary epigastric pain and anorexia) were mild; although we suspected the involvement of ICI at that time, CMV infection should have been mentioned as a differential diagnosis because immunosuppression is often observed in patients receiving chemotherapy, especially ICIs. Therefore, CMV antigen tests and tissue immunostaining should have been performed to exclude the possibility of CMV infection at the time of treatment.

Other differential diseases include H. pylori-associated gastritis, radiation gastritis, drug-induced gastritis, and Zollinger–Ellison syndrome. This patient was treated for H. pylori infection, had no history of radiation therapy, and had no newly introduced drugs. However, serum gastrin levels had not been measured before; subsequently, the possibility of Zollinger–Ellison syndrome could not be completely ruled out. The possibility of malignant proliferative disease, such as cancer or lymphoma, was ruled out by the histological diagnosis and clinical course.

To our knowledge, this is the first report of observable improvements in both gastric mucosal and histopathological findings over time as ICI administration was discontinued. We believe that these results provide strong support for the idea that ICI administration causes immune abnormalities in patients. Although the presented patient had few subjective symptoms, the inflamed gastric mucosa had extensive erosions with diffuse white exudate deposits, mainly in the gastric body. Referring to previous reports, this finding occurred in more than 40% of patients with gastritis after ICI administration. In future, when patients receiving ICIs complain of abdominal symptoms, aggressive tissue biopsy and immuno-histochemical staining should be performed in addition to endoscopy to provide characteristic endoscopic and histological findings that are useful for diagnosis.