Management of immune-related hepatitis in patients being treated with checkpoint inhibitors for metastatic melanoma, a review and case series

被引:4
作者
Tew, Alice [1 ]
Khoja, Leila [1 ,2 ]
Pallan, Lalit [1 ]
Steven, Neil [1 ,2 ]
机构
[1] Queen Elizabeth Hosp, Univ Hosp Birmingham NHS Fdn Trust, Dept Oncol, Birmingham B15 2TH, England
[2] Univ Birmingham, Coll Med & Dent Sci, Inst Immunol & Immunotherapy, Birmingham, England
关键词
Checkpoint inhibitors; immune-related adverse events; immune-related hepatitis; melanoma; tacrolimus; ADVERSE EVENTS; COMBINED NIVOLUMAB; IPILIMUMAB; IMMUNOTHERAPY; SURVIVAL;
D O I
10.1177/10781552221103548
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Immune-related hepatitis is an adverse effect following treatment with immune-checkpoint inhibitors, such as ipilimumab, nivolumab and pembrolizumab. International guidelines advise on the use of corticosteroids as first-line treatment, although guidance on how to treat cases resistant to corticosteroids is limited. We aimed to evaluate the presentation and management of patients with grade 3-4 immune-related hepatitis, following treatment with immune-checkpoint inhibitors for stage 4 or unresectable or stage 3 melanoma, with a particular focus on steroid-refractory cases. Methods A retrospective observational review of patients developing immune-related hepatitis whilst undergoing treatment with immune checkpoint inhibitors for advanced melanoma from July 2014 to February 2020 at a tertiary oncology centre. Results Forty-one patients developed immune-related hepatitis, of which 83% had been treated with the combination of ipilimumab and nivolumab. The median time to onset of IR-hepatitis was 47 days (range: 4-476), and the median time to peak alanine aminotransferase was 71 days (range: 4-478). Four patients had resolution of grade 3 immune-related hepatitis without the introduction of corticosteroids. A total of 37 patients were treated with corticosteroids. A total of 12 required oral treatment only and 13 were successfully managed as outpatients. Six patients had steroid-refractory immune-related hepatitis; and all received tacrolimus, with one also receiving mycophenolate mofetil and infliximab. Conclusions This study describes the largest UK series of immune-related hepatitis patients in the literature. We present two important deviations from current guidelines. Firstly, there is some evidence that withholding steroids is possible in grade 3-4 immune-related hepatitis. Secondly, tacrolimus can be used successfully to manage patients resistant to corticosteroids, with the early introduction most beneficial to reduce time on steroids.
引用
收藏
页码:1163 / 1171
页数:9
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