Ladouceur Alexandra, Barnetche Thomas, Prey Sorilla, Dutriaux Caroline, Gerard Émilie, Pham-Ledard Anne, Beylot-Barry Marie, Zysman Maeva, Veillon Rémi, Domblides Charlotte, Daste Amaury, Gross-Goupil Marine, Sionneau Baptiste, Lefort Felix, Mathieu Larroquette, Richez Christophe, Truchetet Marie-Elise, Schaeverbeke Thierry, Kostine Marie
Department of Rheumatology, Hôpital Pellegrin, place Amélie-Raba-Léon, 33000 Bordeaux, France; Department of Medicine, McGill University, 845, rue Sherbrooke Ouest, Montréal, QC H3A 0G4, Canada.
Department of Rheumatology, Hôpital Pellegrin, place Amélie-Raba-Léon, 33000 Bordeaux, France.
Joint Bone Spine. 2025 Jan;92(1):105795. doi: 10.1016/j.jbspin.2024.105795. Epub 2024 Oct 22.
Immune checkpoint inhibitors-induced inflammatory arthritis (ICI-IA) affects about 5% of ICI recipients. We aimed (1) to characterize the resolution of ICI-IA during ICI treatment and after ICI discontinuation and (2) to assess how ICI-IA influences ICI management across time.
All ICI-treated patients referred to rheumatology at Bordeaux University Hospital were identified and patients with ICI-IA with a follow-up of≥6months after ICI-IA onset were included. Resolution of ICI-IA was defined by discontinuation of ICI-IA medications without recurrence of ICI-IA symptoms.
Resolution of ICI-IA occurred in 13 of 80 patients (16%) while maintaining active ICI treatment, mainly in patients with polymyalgia rheumatica (PMR)-like clinical presentation (P=0.03). Synovitis was more frequent in those whose ICI-IA persisted throughout ICI treatment. In patients with persistent ICI-IA throughout ICI treatment, 34 (50%) and 47 (70%) resolved at 6- and 12-months post-ICI discontinuation, respectively. Reason for terminating ICI was more frequently cancer stable or in remission in those who still had active ICI-IA at 6- and 12-months post-ICI discontinuation. Both progression-free survival and overall survival were longer in the groups with active ICI-IA at 6- and 12-months after ICI discontinuation.
In this cohort, ICI was safely continued in most patients experiencing ICI-IA. About one sixth of ICI-IA resolved despite maintaining active ICI treatment and allowing ICI-IA treatment discontinuation without recurrence of symptoms, mainly in those with PMR-like presentation. Larger studies are needed to determine predicting factors of resolving ICI-IA to minimize exposure to immunosuppressive treatment.
免疫检查点抑制剂诱发的炎性关节炎(ICI-IA)影响约5%接受ICI治疗的患者。我们旨在(1)描述ICI治疗期间及ICI停药后ICI-IA的缓解情况,以及(2)评估ICI-IA如何随时间影响ICI治疗管理。
确定所有转诊至波尔多大学医院风湿科接受ICI治疗的患者,并纳入ICI-IA发病后随访≥6个月的患者。ICI-IA的缓解定义为停用ICI-IA药物且ICI-IA症状未复发。
80例患者中有13例(16%)在维持ICI积极治疗期间出现ICI-IA缓解,主要是具有风湿性多肌痛(PMR)样临床表现的患者(P=0.03)。在整个ICI治疗期间ICI-IA持续存在的患者中,滑膜炎更为常见。在整个ICI治疗期间ICI-IA持续存在的患者中,分别有34例(50%)和47例(70%)在ICI停药后6个月和12个月时缓解。在ICI停药后6个月和12个月仍有活动性ICI-IA的患者中,终止ICI的更常见原因是癌症病情稳定或缓解。在ICI停药后6个月和12个月时患有活动性ICI-IA的组中,无进展生存期和总生存期均更长。
在该队列中,大多数发生ICI-IA的患者可安全地继续使用ICI。尽管维持ICI积极治疗并允许停用ICI-IA治疗且症状未复发,但仍有大约六分之一的ICI-IA得到缓解,主要发生在具有PMR样表现的患者中。需要开展更大规模的研究以确定ICI-IA缓解的预测因素,从而尽量减少免疫抑制治疗的暴露。