Université Paris Saclay, AP-HP, Hôpital de Bicêtre, Department of Internal Medicine, UMR 1184, CEA INSERM, Le Kremlin Bicêtre, France.
Department of thoracic oncology, Gustave Roussy, F-94800 Villejuif, France.
Respir Med Res. 2022 Nov;82:100969. doi: 10.1016/j.resmer.2022.100969. Epub 2022 Nov 9.
Anticancer immune-checkpoint inhibitors (ICI) can cause immune-related adverse events (irAEs), including interstitial pneumonitis, which is managed chiefly with systemic corticosteroids. When corticosteroids fail, second-line immunosuppressive therapy is indicated. Our objective was to evaluate the prevalence and outcomes of ICI-induced pneumonitis requiring second-line immunosuppressive therapy (IS).
We collected data form the REISAMIC pharmacovigilance registry and the multidisciplinary immunological toxicity board at Gustave Roussy (France). No response to steroids was called steroid-refractory pneumonitis and relapse after an initial response was defined as steroid-resistant pneumonitis.
Of the 1187 patients screened from the REISAMIC register, 48 (4%) patients had pneumonitis treated with corticosteroids. Five of them (10%) had corticosteroid refractory/resistant disease but only 2 were treated with immunosuppressive therapy. Four additional patients requiring immunosuppressive therapy identified via the immunological toxicity board were included. Immunosuppressive therapy were cyclophosphamide (n=4 pts), infliximab (n=1 pt), intravenous immunoglobulins (n=1 pt). Five of these six patients had corticosteroid-refractory disease and one had corticosteroid-resistant pneumonitis. Five patients had severe pneumonitis (Common Terminology Criteria for Adverse Events grade ≥3) at initial pneumonitis diagnosis. Two months mortality rate in patients treated with IS was 67% (4/6). Among the patients treated with IS, the two patients alive at 5 months were treated with cyclophosphamide.
Patients with ICI-pneumonitis treated by steroids received IS in 10% of cases. High mortality at 67% of patients was observed in ICI-pneumonitis after steroid failure. Cyclophosphamide could be a treatment option for pneumonitis after corticosteroid failure that requires further investigations.
抗癌免疫检查点抑制剂(ICI)可引起免疫相关不良反应(irAEs),包括间质性肺炎,主要采用全身皮质类固醇治疗。皮质类固醇治疗失败后,需要二线免疫抑制治疗。我们的目的是评估需要二线免疫抑制治疗(IS)的 ICI 诱导性肺炎的发生率和结局。
我们从法国古斯塔夫·鲁西(Gustave Roussy)的 REISAMIC 药物警戒登记处和多学科免疫毒性委员会收集数据。对类固醇无反应称为类固醇难治性肺炎,初始反应后复发定义为类固醇耐药性肺炎。
从 REISAMIC 登记处筛选的 1187 例患者中,48 例(4%)患者接受皮质类固醇治疗的肺炎。其中 5 例(10%)患有皮质类固醇难治/耐药疾病,但仅 2 例接受免疫抑制治疗。通过免疫毒性委员会还确定了另外 4 例需要免疫抑制治疗的患者。免疫抑制治疗包括环磷酰胺(n=4 例)、英夫利昔单抗(n=1 例)、静脉注射免疫球蛋白(n=1 例)。这 6 例患者中有 5 例为皮质类固醇难治性疾病,1 例为皮质类固醇耐药性肺炎。5 例患者在初始肺炎诊断时患有严重肺炎(不良事件通用术语标准≥3 级)。接受 IS 治疗的患者 2 个月死亡率为 67%(4/6)。在接受 IS 治疗的患者中,2 例存活 5 个月的患者接受环磷酰胺治疗。
接受皮质类固醇治疗的 ICI 肺炎患者中,有 10%接受了 IS 治疗。皮质类固醇治疗失败后 ICI 肺炎患者的死亡率为 67%,较高。环磷酰胺可能是皮质类固醇治疗失败后需要进一步研究的肺炎的治疗选择。