4.7 Article

Oral beclomethasone dipropionate is an effective treatment for immune checkpoint inhibitor induced colitis

Journal

JOURNAL FOR IMMUNOTHERAPY OF CANCER
Volume 10, Issue 9, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jitc-2022-005490

Keywords

Inflammation; Immunotherapy

Funding

  1. National Institute of Health Research (NIHR) Biomedical Research Centre based at Imperial College London and Imperial College Healthcare NHS Trust
  2. NIHR Academic Clinical Lectureship
  3. Imperial College London
  4. Joyce and Norman Freed Charitable Trust
  5. National Institute of Health Research (NIHR) Biomedical Research Centre based at the Royal Marsden
  6. ICR

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This study aimed to evaluate the efficacy of the topically acting oral corticosteroid beclomethasone dipropionate (BD) in treating CPI-induced colitis. The results of the study showed that BD treatment was effective and safe in treating this condition. In patients with CPI-induced colitis, BD induced remission and restored baseline stool frequency.
Introduction Systemic corticosteroids are the mainstay of treatment for immune checkpoint inhibitor induced (CPI) colitis but are associated with complications including life-threatening infection. The topically acting oral corticosteroid beclomethasone dipropionate (BD) is an effective treatment for mild to moderate flares of ulcerative colitis, and has fewer side effects than systemic corticosteroids. We hypothesized that BD would be an effective treatment for CPI-induced colitis. Methods We performed a retrospective analysis of all patients who started BD for CPI-induced colitis at three UK cancer centers between November 2017 and October 2020. All patients underwent endoscopic assessment and biopsy. The initial regimen of BD was 5 mg once daily for 28 days. Data were collected from electronic patient records. Clinical outcomes were assessed at 28 days after initiation of treatment. Results Twenty-two patients (14 male) with a median age of 64 (range 45-84) with CPI-induced colitis were treated with BD. At baseline, the median number of loose stools in a 24-hour period was six (common terminology criteria for adverse events, CTCAE grade diarrhea=2). Thirteen patients (59%) were dependent on systemic corticosteroids prior to starting BD. Baseline sigmoidoscopy showed moderate inflammation (Mayo Endoscopic Score (MES) = 2) in two patients (9%), mild inflammation (MES=1) in nine patients (41%) and normal findings (MES=0) in eleven patients (50%). Twenty patients (91%) had histopathological features of inflammation. All 22 patients (100%) had a clinical response to BD and 21 (95%) achieved clinical remission with a return to baseline stool frequency (CTCAE diarrhea=0). Ten patients (45%) had symptomatic relapse on cessation of BD, half within 7 days of stopping. All patients recaptured response on restarting BD. No adverse events were reported in patients treated with BD. Conclusions Topical BD represents an appealing alternative option to systemic immunosuppressive treatments to treat colonic inflammation. In this study, BD was effective and safe at inducing remission in CPI-induced colitis, which was refractory to systemic corticosteroids. Further randomized studies are needed to confirm these findings and determine the optimum dosing regimen.

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