Efficiency and Toxicity of Imatinib Mesylate Combined with Atorvastatin Calcium in the Treatment of Steroid-Refractory Chronic Graft-versus-Host Disease: A Single-Center, Prospective, Single-Arm, Open-Label Study.

IF 1.7 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2024-02-16 DOI:10.1159/000536174
Ting Chen, JiaLi Li, Xiao Wei, Han Yao, LiDan Zhu, Jia Liu, YuQing Liu, Ping Wang, YiMei Feng, ShiChun Gao, HuanFeng Liu, Lu Wang, Lu Zhao, Li Gao, Cheng Zhang, Lei Gao, Xi Zhang, PeiYan Kong
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引用次数: 0

Abstract

Introduction: Steroid-refractory cGVHD (SR-cGVHD) presents new great challenges for treatment. We have reported that imatinib monotherapy was effective to SR-cGVHD, but the CR rate was not satisfactory and the benefit was not showed specific to some target organs, previously. Imatinib and statin drugs have been recognized to regulate T-cell function, statins also have been demonstrated endothelia protection, but whether this combination therapy was able to improve the efficacy remains unknown. Therefore, we designed this prospective, single-arm, open-label trial to investigate the efficacy of imatinib-based combination therapy in the treatment of SR-cGVHD for the first time.

Methods: Sixty SR-cGVHD patients were entered into this trial to investigate the combination of imatinib mesylate and atorvastatin calcium for the treatment of SR-cGVHD. The primary endpoint included the overall response rate (ORR) after 6 months of combined treatment. The secondary endpoints included an evaluation of survival, changes in T-cell subsets, and adverse events.

Results: At baseline, 45% (27/60) of patients had moderate cGVHD, and 55.0% (33/60) of patients had severe cGVHD. At the 6-month follow-up, a clinical response was achieved in 70.0% of patients, and a complete response (CR) was achieved in 26.7%. A total of 11.7% (7/60) of patients stopped immunosuppressive therapy at this point. After 6 months of treatment, the ORR rates of the liver, skin, eyes, and oral cavity were 80.6%, 78.1%, 61.5%, and 60.9%, respectively, with the liver also having the highest CR of 58.1%. The patients with moderate cGVHD had a better CR rate than those with severe cGVHD (55.6% vs. 3.0%, p < 0.0001). The overall survival in patients with ORR was improved (p = 0.0106). Lung involvement is an independent risk factor to affected ORR achievement (p = 0.021, HR = 0.335, 95% CI: 0.133-0.847), and the dosage of steroids was reduced in ORR patients. In clinical response patients, the ratio of CD8+ T cells (p = 0.0117) and Th17 cells (p = 0.0171) decreased, while the number of Treg cells (p = 0.0147) increased after 3 months. The most common adverse events were edema, nausea, and neutropenia, which were 13.3%, 11.7%, and 11.7%, respectively.

Conclusion: Combination treatment with imatinib mesylate and atorvastatin calcium was effective in treating SR-cGVHD and significantly decreased target organ injury, especially liver damage, indicating that T-cell regulatory function may play an important role in this process.

甲磺酸伊马替尼联合阿托伐他汀钙治疗类固醇难治性慢性移植物抗宿主病的疗效和毒性:一项单中心、前瞻性、单臂、开放标签研究。
导言:类固醇难治性 cGVHD(SR-cGVHD)给治疗带来了新的巨大挑战。此前,我们曾报道伊马替尼单药治疗对SR-cGVHD有效,但CR率并不令人满意,对某些靶器官也未显示出特异性获益。伊马替尼和他汀类药物被认为可以调节 T 细胞功能,他汀类药物还被证实具有内皮细胞保护作用,但这种联合疗法是否能提高疗效仍是未知数。因此,我们设计了这项前瞻性、单臂、开放标签试验,首次研究以伊马替尼为基础的联合疗法治疗SR-cGVHD的疗效。方法:60例SR-cGVHD患者进入该试验,研究甲磺酸伊马替尼和阿托伐他汀钙联合治疗SR-cGVHD。主要终点包括联合治疗6个月后的总反应率(ORR)。次要终点包括生存期评估、T细胞亚群变化和不良事件:基线时,45%(27/60)的患者患有中度cGVHD,55.0%(33/60)的患者患有重度cGVHD。在6个月的随访中,70.0%的患者获得了临床应答,26.7%的患者获得了完全应答(CR)。此时,共有 11.7% 的患者(7/60)停止了免疫抑制治疗。治疗 6 个月后,肝脏、皮肤、眼睛和口腔的 ORR 率分别为 80.6%、78.1%、61.5% 和 60.9%,其中肝脏的 CR 率最高,为 58.1%。中度cGVHD患者的CR率高于重度cGVHD患者(55.6%对3.0%):甲磺酸伊马替尼和阿托伐他汀钙联合治疗可有效治疗SR-cGVHD,并显著减少靶器官损伤,尤其是肝损伤,这表明T细胞调节功能可能在这一过程中发挥了重要作用。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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