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西利单抗治疗镰状细胞病患者的药代动力学、药效学、安全性和疗效。

Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease.

机构信息

Division of Hematology and Oncology, University of Alabama, Birmingham, AL.

Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA.

出版信息

Blood Adv. 2023 Mar 28;7(6):943-952. doi: 10.1182/bloodadvances.2022008209.

DOI:10.1182/bloodadvances.2022008209
PMID:36355805
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10027508/
Abstract

Crizanlizumab is an anti-P-selectin monoclonal antibody indicated to reduce the frequency/prevent recurrence of vaso-occlusive crises (VOCs) in patients with sickle cell disease (SCD) aged ≥16 years. This analysis of an ongoing phase 2, nonrandomized, open-label study reports the pharmacokinetics (PK), pharmacodynamics (PD), safety, and efficacy of crizanlizumab 5.0 mg/kg (N = 45) and 7.5 mg/kg (N = 12) in patients with SCD with a history of VOCs. The median treatment duration was 104.7 and 85.7 weeks in the 5.0 and 7.5 mg/kg groups, respectively. For both doses, serum crizanlizumab concentrations rose to near maximum levels shortly after infusion, and near complete and sustained ex vivo P-selectin inhibition was observed. Grade ≥3 adverse events (AEs) occurred in 48.9% and 33.3% of patients in the 5.0 and 7.5 mg/kg groups, respectively; only 1 event was deemed treatment-related (7.5 mg/kg group). No treatment-related serious AEs occurred. One infusion-related reaction was recorded (5.0 mg/kg, grade 2 "pain during infusion"), which resolved without treatment withdrawal. Infections occurred in 57.8% and 41.7% of patients in the 5.0 and 7.5 mg/kg groups, respectively; none were drug-related. No treatment-related bleeding events were reported. No patients developed immunogenicity. The median (range) absolute reduction from baseline in the annualized rate of VOCs leading to a health care visit was -0.88 (-14.7 to 13.3) and -0.93 (-2.0 to 0.4) in the 5.0 and 7.5 mg/kg groups, respectively. Results here demonstrate the PK/PD properties of crizanlizumab in patients with SCD and the potential sustained efficacy and long-term safety of the drug after >12 months' treatment. This trial was registered at www.clinicaltrials.gov as #NCT03264989.

摘要

Crizanlizumab 是一种抗 P-选择素单克隆抗体,用于减少 16 岁及以上镰状细胞病 (SCD) 患者血管阻塞性危象 (VOC) 的发作频率/预防复发。这项正在进行的 2 期、非随机、开放标签研究的分析报告了既往有 VOC 病史的 SCD 患者接受 5.0mg/kg(N=45)和 7.5mg/kg(N=12)crizanlizumab 的药代动力学(PK)、药效学(PD)、安全性和疗效。5.0mg/kg 和 7.5mg/kg 组的中位治疗持续时间分别为 104.7 周和 85.7 周。对于这两种剂量,血清 crizanlizumab 浓度在输注后不久即升高至接近最大水平,并且观察到近乎完全和持续的体外 P-选择素抑制。5.0mg/kg 和 7.5mg/kg 组分别有 48.9%和 33.3%的患者发生≥3 级不良事件(AE);仅有 1 例事件被认为与治疗相关(7.5mg/kg 组)。无治疗相关严重 AE 发生。记录到 1 例输注相关反应(5.0mg/kg,2 级“输注时疼痛”),无需停药即可缓解。5.0mg/kg 和 7.5mg/kg 组分别有 57.8%和 41.7%的患者发生感染;均与药物无关。无治疗相关出血事件报告。无患者发生免疫原性。与基线相比,5.0mg/kg 和 7.5mg/kg 组年化 VOC 发生率降低导致就诊的绝对值分别为-0.88(-14.7 至 13.3)和-0.93(-2.0 至 0.4)。这些结果表明,crizanlizumab 在 SCD 患者中的 PK/PD 特性,以及该药在治疗 12 个月以上后的潜在持续疗效和长期安全性。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT03264989。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/86de117390a4/BLOODA_ADV-2022-008209-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/1169ce3d3cd0/BLOODA_ADV-2022-008209-fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/cf3a43822f06/BLOODA_ADV-2022-008209-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/d8abf3f888af/BLOODA_ADV-2022-008209-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/98fd361f6e11/BLOODA_ADV-2022-008209-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/86de117390a4/BLOODA_ADV-2022-008209-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/1169ce3d3cd0/BLOODA_ADV-2022-008209-fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/cf3a43822f06/BLOODA_ADV-2022-008209-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/d8abf3f888af/BLOODA_ADV-2022-008209-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/98fd361f6e11/BLOODA_ADV-2022-008209-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e9/10027508/86de117390a4/BLOODA_ADV-2022-008209-gr4.jpg

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本文引用的文献

1
American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain.美国血液学会2020年镰状细胞病指南:急性和慢性疼痛的管理
Blood Adv. 2020 Jun 23;4(12):2656-2701. doi: 10.1182/bloodadvances.2020001851.
2
Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy.镰状细胞病中的补体激活:依赖于细胞密度、溶血和羟脲治疗的调节。
Am J Hematol. 2020 May;95(5):456-464. doi: 10.1002/ajh.25742. Epub 2020 Feb 19.
3
The importance of early identification of infusion-related reactions to monoclonal antibodies.
The Current Role of Hydroxyurea in the Treatment of Sickle Cell Anemia.
羟基脲在镰状细胞贫血治疗中的当前作用
J Clin Med. 2024 Oct 25;13(21):6404. doi: 10.3390/jcm13216404.
4
Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease: final results from the phase II SOLACE-adults study.crizanlizumab治疗镰状细胞病患者的药代动力学、药效学、安全性及疗效:II期SOLACE-成人研究的最终结果
Ther Adv Hematol. 2024 Nov 3;15:20406207241292508. doi: 10.1177/20406207241292508. eCollection 2024.
5
Real-World Evidence of Crizanlizumab Showing Reductions in Vaso-Occlusive Crises and Opioid Usage in Sickle Cell Disease.克立硐珠单抗在镰状细胞病中减少血管闭塞性危象和阿片类药物使用的真实世界证据。
Eur J Haematol. 2025 Feb;114(2):293-302. doi: 10.1111/ejh.14323. Epub 2024 Oct 29.
6
Newer Modalities and Updates in the Management of Sickle Cell Disease: A Systematic Review.镰状细胞病管理中的新型治疗方法与进展:一项系统综述
J Blood Med. 2024 Sep 12;15:435-447. doi: 10.2147/JBM.S477507. eCollection 2024.
7
Budget Impact of Disease-Modifying Treatments and a CRISPR Gene-Edited Therapy for Sickle Cell Disease.用于治疗镰状细胞病的疾病修正治疗和 CRISPR 基因编辑疗法的预算影响。
Clin Drug Investig. 2024 Aug;44(8):611-627. doi: 10.1007/s40261-024-01384-w. Epub 2024 Aug 12.
8
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9
Using disease-modifying therapies in sickle cell disease.在镰状细胞病中使用疾病修正疗法。
Hematology Am Soc Hematol Educ Program. 2023 Dec 8;2023(1):519-531. doi: 10.1182/hematology.2023000485.
10
The challenge of clinical end points in sickle cell disease.镰状细胞病临床终点的挑战。
Blood. 2023 Dec 14;142(24):2047-2054. doi: 10.1182/blood.2023021220.
早期识别单克隆抗体输注相关反应的重要性。
Ther Clin Risk Manag. 2019 Aug 1;15:965-977. doi: 10.2147/TCRM.S204909. eCollection 2019.
4
Sickle cell disease complications: Prevalence and resource utilization.镰状细胞病并发症:患病率和资源利用。
PLoS One. 2019 Jul 5;14(7):e0214355. doi: 10.1371/journal.pone.0214355. eCollection 2019.
5
Sickle cell disease.镰状细胞病。
Nat Rev Dis Primers. 2018 Mar 15;4:18010. doi: 10.1038/nrdp.2018.10.
6
Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease.克立硃单抗用于预防镰状细胞病的疼痛危象
N Engl J Med. 2017 Feb 2;376(5):429-439. doi: 10.1056/NEJMoa1611770. Epub 2016 Dec 3.
7
Clinical development methodology for infusion-related reactions with monoclonal antibodies.单克隆抗体输注相关反应的临床开发方法。
Clin Transl Immunology. 2015 Jul 17;4(7):e39. doi: 10.1038/cti.2015.14. eCollection 2015 Jul.
8
Vaso-occlusion in sickle cell disease: pathophysiology and novel targeted therapies.镰状细胞病中的血管闭塞:病理生理学和新型靶向治疗。
Blood. 2013 Dec 5;122(24):3892-8. doi: 10.1182/blood-2013-05-498311. Epub 2013 Sep 19.
9
Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease.疼痛程度和社会环境而非累积的器官损伤决定了镰状细胞病成年患者的生活质量。
Am J Hematol. 2010 Jul;85(7):532-5. doi: 10.1002/ajh.21731.
10
Safety and immunotoxicity assessment of immunomodulatory monoclonal antibodies.免疫调节单克隆抗体的安全性和免疫毒性评估。
MAbs. 2010 May-Jun;2(3):233-55. doi: 10.4161/mabs.2.3.11782. Epub 2010 May 23.