Toffart Anne-Claire, Meert Anne-Pascale, Wallet Florent, Gibelin Aude, Guisset Olivier, Gonzalez Frédéric, Seguin Amélie, Kouatchet Achille, Delaunay Myriam, Debieuvre Didier, Duchemann Boris, Rousseau-Bussac Gaëlle, Nyunga Martine, Grimaldi David, Levrat Albrice, Azoulay Elie, Lemiale Virginie
Department of Pneumology and Physiology, CHU Grenoble Alpes, Grenoble, France.
Department of Internal Medicine, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Ann Intensive Care. 2023 Apr 18;13(1):29. doi: 10.1186/s13613-023-01122-z.
Immune checkpoint inhibitors (ICI) have revolutionized the management of cancer. They can induce immune-related adverse events (irAE) leading to intensive care unit (ICU) admission. We aimed to describe irAEs for ICU admissions in solid cancer patients treated with ICIs.
This prospective multicenter study was conducted in France and Belgium. Adult patients with solid tumor and treated with systemic ICIs within the last 6 months, requiring non-programmed ICU admission were included. Patients admitted for microbiologically documented sepsis were excluded. Imputability of irAEs in ICU admissions was described according to the WHO-UMC classification system at ICU admission and at ICU discharge. The use of immunosuppressant treatment was reported.
115 patients were eligible. Solid tumor was mainly lung cancer (n = 76, 66%) and melanoma (n = 18, 16%). They were mainly treated with an anti-PD-(L)1 alone (n = 110, 96%). Main ICU admission reasons were acute respiratory failure (n = 66, 57%), colitis (n = 14, 13%), and cardiovascular disease (n = 13, 11%). ICU admission was considered "likely" associated with irAE for 48% (n = 55) of patients. Factors independently associated with irAE were a good ECOG performance status (PS) (ECOG-PS of 0 or 1 vs. ECOG-PS of 2-3, odds ratio [OR] = 6.34, 95% confidence interval [95% CI] 2.13-18.90, and OR = 3.66, 95% CI 1.33-10.03, respectively), and a history of irAE (OR = 3.28, 95% CI 1.19-9.01). Steroids were prescribed for 41/55 (75%) patients with ICU admission "likely" related to irAE. Three patients were subsequently treated with immunosuppressants.
IrAEs accounted for half of ICU admissions in cancer patients receiving ICIs. They could be treated with steroids. Identifying the imputability of irAEs in ICU admissions remains a challenge.
免疫检查点抑制剂(ICI)彻底改变了癌症的治疗方式。它们可引发免疫相关不良事件(irAE),导致患者入住重症监护病房(ICU)。我们旨在描述接受ICI治疗的实体癌患者入住ICU的irAE情况。
这项前瞻性多中心研究在法国和比利时开展。纳入过去6个月内接受全身ICI治疗、需要非计划性入住ICU的成年实体瘤患者。排除因微生物学确诊的败血症而入院的患者。根据WHO-UMC分类系统,在患者入住ICU时及出院时描述irAE在ICU入院中的可归因性。报告免疫抑制剂治疗的使用情况。
115例患者符合条件。实体瘤主要为肺癌(n = 76,66%)和黑色素瘤(n = 18,16%)。他们主要单独接受抗PD-(L)1治疗(n = 110,96%)。入住ICU的主要原因是急性呼吸衰竭(n = 66,57%)、结肠炎(n = 14,13%)和心血管疾病(n = 13,11%)。48%(n = 55)的患者入住ICU被认为“可能”与irAE相关。与irAE独立相关的因素包括良好的东部肿瘤协作组(ECOG)体能状态(PS)(ECOG-PS为0或1与ECOG-PS为2-3相比,比值比[OR]分别为6.34,95%置信区间[95%CI]2.13-18.90和OR为3.66,95%CI 1.33-10.03)以及irAE病史(OR = 3.28,95%CI 1.19-9.01)。41/55(75%)入住ICU“可能”与irAE相关的患者接受了类固醇治疗。3例患者随后接受了免疫抑制剂治疗。
irAE占接受ICI治疗的癌症患者入住ICU原因的一半。它们可用类固醇治疗。确定irAE在ICU入院中的可归因性仍然是一项挑战。