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伊布替尼治疗类固醇难治性慢性移植物抗宿主病:一项多中心真实世界分析。

Ibrutinib for therapy of steroid-refractory chronic graft-versus-host disease: a multicenter real-world analysis.

作者信息

Pidala Joseph, Kim Jongphil, Kalos Denise, Cutler Corey, DeFilipp Zachariah, Flowers Mary E D, Hamilton Betty K, Chin Kuo-Kai, Rotta Marcello, El Jurdi Najla, Hamadani Mehdi, Ahmed Gulrayz, Kitko Carrie, Ponce Doris, Sung Anthony, Tang Helen, Farhadfar Nosha, Nemecek Eneida, Pusic Iskra, Qayed Muna, Rangarajan Hemalatha, Hogan William, Etra Aaron, Jaglowski Samantha

机构信息

Department of Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.

出版信息

Blood Adv. 2025 Mar 11;9(5):1040-1048. doi: 10.1182/bloodadvances.2024014374.

Abstract

To examine the activity of ibrutinib in steroid-refractory chronic graft-versus-host disease (SR-cGVHD) after the US Food and Drug Administration approval, we conducted a multicenter retrospective study. Data were standardly collected (N = 270 from 19 centers). Involved organs included skin (75%), eye (61%), mouth (54%), joint/fascia (47%), gastrointestinal (GI) (26%), lung (27%), liver (19%), genital (7%), and others (4.4%). The National Institutes of Health (NIH) severity was mild in 5.7%, moderate 42%, and severe 53%. Thirty-nine percent had overlap subtype. Karnofsky performance status (KPS) was ≥80% in 72%. The median prednisone was 0.21 mg/kg (0-2.27). Ibrutinib was started at a median of 18.2 months after cGVHD onset and in earlier lines of therapy (second line, 26%; third, 30%; fourth, 21%; fifth, 9.6%; sixth, 10%; seventh or higher, 1.2%). Among evaluable patients, the 6-month NIH overall response rate (ORR; complete response [CR]/partial response [PR]) was 45% (PR 42%; CR 3%). The median duration of response was 15 months (range, 1-46). Liver involvement had association with 6-month ORR (multivariate [MVA] odds ratio, 5.49; 95% confidence interval [CI], 2.3-14.2; P < .001). The best overall response was 56%, with most (86%) achieving by 1 to 3 months. With a median follow-up for survivors of 30.5 months, failure-free survival (FFS) was 59% (53%-65%) at 6 months and 41% (36%-48%) at 12 months. On MVA, increased age (hazard ratio [HR], 1.01; 95% CI, 1.0-1.02; P = .033), higher baseline prednisone (HR, 1.92; 95% CI, 1.09-3.38; P = .032), and lung involvement (HR, 1.58; 95% CI, 1.1-2.28; P = .016) had worse FFS. Ibrutinib discontinuation was most commonly due to progressive cGVHD (44%) or toxicity (42%). These data support that ibrutinib has activity in SR-cGVHD, provide new insight into factors associated with response and FFS, and demonstrate the toxicity profile associated with discontinuation.

摘要

在美国食品药品监督管理局批准后,为研究依鲁替尼在类固醇难治性慢性移植物抗宿主病(SR-cGVHD)中的活性,我们开展了一项多中心回顾性研究。数据按标准收集(来自19个中心,共270例)。受累器官包括皮肤(75%)、眼睛(61%)、口腔(54%)、关节/筋膜(47%)、胃肠道(GI)(26%)、肺(27%)、肝脏(19%)、生殖器(7%)及其他(4.4%)。美国国立卫生研究院(NIH)疾病严重程度分级为轻度占5.7%,中度占42%,重度占53%。39%为重叠亚型。卡诺夫斯基功能状态(KPS)≥80%的患者占72%。泼尼松的中位剂量为0.21mg/kg(0 - 2.27)。依鲁替尼在cGVHD发病后中位18.2个月开始使用,且多在早期治疗线次使用(二线,26%;三线,30%;四线,21%;五线,9.6%;六线,10%;七线及以上,1.2%)。在可评估患者中,6个月时NIH总体缓解率(ORR;完全缓解[CR]/部分缓解[PR])为45%(PR 42%;CR 3%)。缓解持续时间的中位数为15个月(范围1 - 46个月)。肝脏受累与6个月ORR相关(多变量[MVA]优势比,5.49;95%置信区间[CI],2.3 - 14.2;P <.001)。最佳总体缓解率为56%,多数(86%)在1至3个月时达到。存活者的中位随访时间为30.5个月,6个月时无失败生存(FFS)率为59%(53% - 65%),12个月时为41%(36% - 48%)。在MVA分析中,年龄增加(风险比[HR],1.01;95% CI,1.0 - 1.02;P =.033)、基线泼尼松剂量较高(HR,1.92;95% CI,1.09 - 3.38;P =.032)以及肺部受累(HR,1.58;95% CI,1.1 - 2.28;P =.016)与FFS较差相关。依鲁替尼停药最常见的原因是cGVHD进展(44%)或毒性(42%)。这些数据支持依鲁替尼在SR-cGVHD中有活性,为与缓解和FFS相关的因素提供了新见解,并展示了与停药相关的毒性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e2e/11909441/caf0158299f4/BLOODA_ADV-2024-014374-ga1.jpg

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