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临床试验/NCT06864481
NCT06864481招募中不适用

Description, Course and Treatment of Immune Checkpoint Inhibitor-induced Hepatitis

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2025年4月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
250
试验地点
1
主要终点
Ratio cholestatic phenotype, cytolytic phenotype and mixed phenotype

研究概览

简要总结

Background and Study Rationale Immune checkpoint inhibitors (ICI) are a breakthrough cancer treatment that boosts the immune system to fight tumors. While effective, they can cause immune-related side effects, including liver inflammation (ICI-induced hepatitis or CHILI), which affects up to 25% of patients. Severe cases requiring treatment discontinuation are rare but challenging to manage.

Study Objective This multicenter prospective study aims to better understand CHILI, its clinical patterns, treatment response, and risk of recurrence. It will focus on different types of liver injury (cholestatic, hepatocellular, or mixed) to guide better treatment decisions.

Innovation and Approach Currently, there is no clear consensus on how to manage CHILI or when to safely restart immunotherapy. This study will collect real-world data from adult patients treated with ICIs, following international guidelines or a pragmatic approach when no consensus exists. Findings will help improve care strategies for patients experiencing ICI-related liver toxicity.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 18 years
  • •Patient willing to participate in the study
  • •Patient with cancer receiving neoadjuvant, adjuvant, or maintenance treatment · Patient treated with ICI, either as monotherapy or in combination with another antitumor treatment (targeted therapy, chemotherapy, or radiotherapy), either de novo or after a first-line treatment including ICIs
  • •Patient who has received at least one injection of an ICI ·
  • •Onset of hepatitis following treatment initiation, defined by the following criteria:
  • •ALT (alanine aminotransferase) ≥ 5 times the upper normal limit
  • •ALP (alkaline phosphatase) ≥ 2 times the upper normal limit
  • •ALT (alanine aminotransferase) ≥ 3 times the upper normal limit and bilirubin ≥ 2 times the upper normal limit ·
  • •Patient with grade 3 or 4 hepatitis, according to the current CTCAE classification

排除标准

  • •Patient with another cause of acute hepatitis, including viral, autoimmune, ischemic, acute alcoholic hepatitis, or Wilson's disease.
  • •Patient unable to express their non-opposition to participate in the study.
  • •Person deprived of liberty, under guardianship or curatorship, or in an emergency situation.
  • •Person not affiliated with a social security system or without entitlement to healthcare coverage.

研究组 & 干预措施

Immune Checkpoint Inhibitor-Induced Hepatitis

Observational cohort

干预措施: Blood samples (Other)

结局指标

主要结局

Ratio cholestatic phenotype, cytolytic phenotype and mixed phenotype

时间窗: Day0, Day14, Day30, Day 90, Month 6 and Month 12

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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