Erkurt Mehmet Ali, Sarici Ahmet, Sahin Abdulkadir, Berber Ilhami, Korkmaz Gulten, Kuku Irfan, Dal Mehmet Sinan, Korkmaz Serdal, Ulas Turgay, Altuntas Fevzi
Inonu University, Faculty of Medicine, Department of Hematology, Malatya, Turkey.
Inonu University, Faculty of Medicine, Department of Hematology, Malatya, Turkey.
Transfus Apher Sci. 2025 Feb;64(1):104052. doi: 10.1016/j.transci.2024.104052. Epub 2024 Dec 16.
Chronic graft-versus-host disease (cGVHD) represents a significant adverse event that may ensue following allogeneic hematopoietic stem cell transplantation (Allo-HSCT). In patients resistant to corticosteroids, which is the first-line treatment for cGVHD, ibrutinib is being evaluated as a potential treatment option. In this study, we aimed to share the findings of our multicenter study regarding the outcomes of ibrutinib treatment in patients with corticosteroid-resistant cGVHD who had previously received multiple systemic therapies.
A retrospective analysis was conducted to examine the clinical characteristics and outcomes of patients who received ibrutinib treatment for corticosteroid-resistant cGVHD after Allo-HSCT.
A total of 24 patients diagnosed with cGVHD who received ibrutinib treatment were included in the study. The median age of the patients was 34.5 (20-67). The included patients were followed for a median of 6 (1-30) months. All patients had stem cells collected from the peripheral blood. Fifty percent of the patients had multiple organ involvement, while the other 50 % had single organ involvement. The most frequently affected organs were skin and liver. On average, patients received four (3-5) lines of systemic therapy before ibrutinib treatment. At week 24 of ibrutinib treatment, 10 patients (41.7 %) had a complete response, and 10 patients (41.7 %) had a partial response; at week 48, 8 patients (33.3 %) had a complete response, and 10 patients (41.7 %) had a partial response. The most common hematological side effect after ibrutinib treatment was thrombocytopenia in 5 out of 24 patients, while the most common non-hematological side effect was CMV infection in 6 out of 24 patients.
In patients with corticosteroid-resistant cGVHD, ibrutinib treatment has been demonstrated to be an efficacious option exhibiting an elevated overall response rate and a tolerable side effect profile.
慢性移植物抗宿主病(cGVHD)是异基因造血干细胞移植(Allo-HSCT)后可能发生的严重不良事件。对于cGVHD的一线治疗药物糖皮质激素耐药的患者,伊布替尼正作为一种潜在的治疗选择进行评估。在本研究中,我们旨在分享多中心研究关于伊布替尼治疗既往接受过多种全身治疗的糖皮质激素耐药性cGVHD患者的结果。
进行回顾性分析,以检查接受伊布替尼治疗Allo-HSCT后糖皮质激素耐药性cGVHD患者的临床特征和结果。
本研究共纳入24例诊断为cGVHD并接受伊布替尼治疗的患者。患者的中位年龄为34.5岁(20 - 67岁)。纳入患者的中位随访时间为6个月(1 - 30个月)。所有患者的干细胞均采集自外周血。50%的患者有多器官受累,另外50%为单器官受累。最常受累的器官是皮肤和肝脏。平均而言,患者在接受伊布替尼治疗前接受了4(3 - 5)线全身治疗。在伊布替尼治疗第24周时,10例患者(41.7%)完全缓解,10例患者(41.7%)部分缓解;在第48周时,8例患者(33.3%)完全缓解,10例患者(41.7%)部分缓解。伊布替尼治疗后最常见的血液学副作用是24例患者中有5例出现血小板减少,最常见的非血液学副作用是24例患者中有6例出现巨细胞病毒感染。
对于糖皮质激素耐药性cGVHD患者,伊布替尼治疗已被证明是一种有效的选择,总体缓解率较高且副作用可耐受。