Volume 78, Issue 4 pp. 532-541
Original Article

Medication-specific variations in morphological patterns of injury in immune check-point inhibitor-associated colitis

Raymond A Isidro

Raymond A Isidro

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

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Alex B Ruan

Alex B Ruan

Harvard Medical School, Boston, MA, USA

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Swetha Gannarapu

Swetha Gannarapu

Division of Gastroenterology, Brigham and Women's Hospital, Boston, MA, USA

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Dhanya Raj

Dhanya Raj

Division of Gastroenterology, Brigham and Women's Hospital, Boston, MA, USA

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Osama Rahma

Osama Rahma

Division of Medical Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

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Shilpa Grover

Shilpa Grover

Division of Gastroenterology, Brigham and Women's Hospital, Boston, MA, USA

These authors share co-senior authorship.Search for more papers by this author
Amitabh Srivastava

Corresponding Author

Amitabh Srivastava

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

These authors share co-senior authorship.

Address for correspondence: A Srivastava, Department of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA. e-mail: [email protected]

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First published: 15 September 2020
Citations: 29

Abstract

Aims

A varied spectrum of histopathological changes has been associated with immune checkpoint inhibitor (ICI) colitis. This study was performed to evaluate the prevalence of different histopathological patterns of injury in patients with ICI colitis and their association with specific immune check-point inhibitors.

Methods and results

Biopsies from patients with clinically and histologically confirmed ICI colitis were reviewed blindly to determine the predominant pattern of injury and to quantitate discrete histological parameters using the Geboes score. Paneth cell metaplasia, intraepithelial lymphocytes, abnormal subepithelial collagen and degree of crypt epithelial apoptosis was also recorded. A total of 86 patients with ICI colitis (ipilimumab, n = 14; ipilimumab + nivolumab, n = 29; nivolumab, n = 20 and pembrolizumab, n = 23) were included. The patterns of injury identified included diffuse active colitis (n = 22), chronic active colitis (n = 22), lymphocytic colitis (LC, n = 16), collagenous colitis (CC, n = 14), graft-versus-host disease-like colitis (n = 7) and mixed colitis (n = 5). Patients on ipilimumab were more likely to have a diffuse active colitis pattern without features of chronicity (P < 0.01) and less likely to have LC (P < 0.05) compared to other ICIs. LC and CC were more common in patients on nivolumab and pembrolizumab relative to other groups (P < 0.05). Chronic active colitis was most frequent in nivolumab patients (P < 0.05), and these patients had received more ICI doses and had been on ICI treatment longer compared to other treatment groups.

Conclusions

ICI colitis should be considered in the differential diagnosis of all the common inflammatory patterns of colitis and shows medication specific differences in patterns of injury.

Conflicts of interest

R.A.I., A.B.R., S.G., D.R. and A.S. have no relevant conflicts of interest. O.R. is an advisory board member for Merck and a speaker for BMS. S.G. is an Editor for Gastroenterology for UpToDate Inc.

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