Acalabrutinib Maleate and Bortezomib for Patients With HLA Antibodies (AB-HLA-2026)
2026年6月7日 更新者:Xuefeng He、The First Affiliated Hospital of Soochow University
Acalabrutinib Maleate Monotherapy or in Combination With Bortezomib for Eliminating HLA Antibodies in Patients With Hematologic Malignancies and Platelet Transfusion Refractoriness: a Multicenter, Randomized Controlled Study
Platelet transfusion refractoriness (PTR) is a common complication in patients with hematological malignancies.
It not only prolongs the duration of platelet transfusion dependence and significantly increases the risk of bleeding, but is also strongly associated with graft failure and reduced survival after transplantation.
HLA class I antibody-mediated alloimmunization is recognized as the most important immunological cause of PTR.
HLA antibodies are directly secreted by plasma cells, which are derived from B cells.
Therefore, targeting B cells to reduce antibody production is a crucial step in eliminating HLA antibodies.
Bruton's tyrosine kinase (BTK) is expressed throughout B cell development from the pre-B cell stage to maturity and supports B cell development, maturation, survival, proliferation, and antibody production by acting as a downstream kinase in the B cell receptor signaling pathway.
Bortezomib, a proteasome inhibitor, can selectively induce apoptosis in long-lived plasma cells.
The investigators' preliminary exploratory use of a BTK inhibitor in the treatment of PTR with HLA antibodies significantly reduced the mean fluorescence intensity (MFI) of HLA antibodies, improved platelet transfusion outcomes, and demonstrated a favorable safety profile.
Based on these findings, the investigators are conducting a prospective, multicenter, randomized controlled two-arm study to investigate the efficacy and safety of acalabrutinib and bortezomib in eliminating HLA antibodies in hematological malignancies patients with PTR.
研究概览
地位
尚未招聘
研究类型
介入性
注册 (估计的)
42
阶段
- 第三阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Yaqiong Tang
- 电话号码:+8618896588075
- 邮箱:tangyaqiong@suda.edu.cn
研究联系人备份
- 姓名:Xuefeng He
- 电话号码:+8618914031640
- 邮箱:hexuefeng@suda.edu.cn
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Patients with hematological malignancies and platelet transfusion refractoriness (24-hour CCI < 4.5×10⁹/L or PPR < 20%), and with the highest MFI of HLA antibodies > 8000 ;
- Age 18-65 years, both male and female;
- ECOG performance status 0-3;
- Expected survival > 6 months;
- Patients must be able to understand and be willing to participate in this study, and sign an informed consent form.
Exclusion Criteria:
- Hypersensitivity to acalabrutinib, bortezomib, or excipients;
- Major organ bleeding (central nervous system, lung, intestines) or grade ≥3 bleeding;
- Hypersplenism;
- Concurrent use of drugs that may cause excessive platelet consumption (amphotericin B, vancomycin, ATG, interferon, etc.);
- Disseminated intravascular coagulation, microangiopathic hemolytic anemia;
- Underlying diseases of vital organs: such as malignant arrhythmia, myocardial infarction, chronic cardiac insufficiency, decompensated liver insufficiency, renal insufficiency, severe coagulation abnormalities, etc.; persistent fever (>38.0°C) for more than 3 days; clinically uncontrolled active infection (including bacterial, fungal, or viral infections), but patients under effective drug therapy are not excluded;
- Concurrent other progressive malignancies;
- Patients with cardiac insufficiency: ejection fraction (EF) <30%, NYHA class ≥III cardiac insufficiency;
- Pregnant or lactating women;
- Expected survival <60 days;
- Currently participating in other clinical drug trials.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Arm A
Acalabrutinib maleate monotherapy or in combination with bortezomib
|
100mg twice a day
1.3mg/m2, d1,4,8,11
Transfusion HLA-matched or crossmatched irradiated platelets 10U if platelet count lower than 10*109/L
0.4g/kg.d for 5 days
|
|
有源比较器:Arm B
Transfusion of HLA-matched or crossmatched irradiated platelets
|
Transfusion HLA-matched or crossmatched irradiated platelets 10U if platelet count lower than 10*109/L
0.4g/kg.d for 5 days
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
The response rate for anti-HLA antibody clearance
大体时间:4 weeks after intervention
|
Complete response: HLA antibody MFI decrease ≥30% (applied to HLA antibody loci with baseline MFI >8000; median value used for assessment) Partial response: HLA antibody MFI decrease ≥10% and <30% No response: HLA antibody MFI decrease <10%, or no decrease or even an increase.
|
4 weeks after intervention
|
|
CCI (corrected count increments)
大体时间:4 weeks after intervention
|
CCI = (platelet increment per ul) x (body surface area in m2)/number of platelets transfused (x 10E11)
|
4 weeks after intervention
|
|
PPR (percentage platelet recovery)
大体时间:4 weeks after intervention
|
PPR = Post-transfusion platelet count-pre-transfusion platelet count (/L) × total blood volume × 100%
|
4 weeks after intervention
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
The incidence of bleeding events
大体时间:The study period (8 weeks after the initiation of intervention)
|
The study period (8 weeks after the initiation of intervention)
|
|
The overall survival rate
大体时间:1 year
|
1 year
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Xuefeng He、The First Affiliated Hospital of Soochow University
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Pan Y, Zuo Y, Cui Q, Liu S, Dai H, Wu D, Jiang M, Tang X. Treatment outcome and efficacy of desensitization strategies for immunized-PTR in hematological malignancies before hematopoietic stem cell transplantation. Bone Marrow Transplant. 2026 Apr;61(4):437-444. doi: 10.1038/s41409-025-02749-1. Epub 2026 Jan 28.
- Van Osch TLJ, Oosterhoff JJ, Bentlage AEH, Nouta J, Koeleman CAM, Geerdes DM, Mok JY, Heidt S, Mulder A, Van Esch WJE, Kapur R, Porcelijn L, Van der Schoot CE, De Haas M, Wuhrer M, Voorberg J, Vidarsson G. Fc galactosylation of anti-platelet human IgG1 alloantibodies enhances complement activation on platelets. Haematologica. 2022 Oct 1;107(10):2432-2444. doi: 10.3324/haematol.2021.280493.
- Couvidou A, Rojas-Jimenez G, Dupuis A, Maitre B. Anti-HLA Class I alloantibodies in platelet transfusion refractoriness: From mechanisms and determinants to therapeutic prospects. Front Immunol. 2023 Feb 9;14:1125367. doi: 10.3389/fimmu.2023.1125367. eCollection 2023.
- Boothby AB, Tanner MK, Alswied A, Youngs D, Bribiesca Rodriguez J, Bikkani T, Cha N, Gernsheimer T, Gimferrer I, Hess JR, Sokol-Hessner L, Marivada S, Nash MG, Flegel WA, Vassallo RR, Stroncek DF, Tsang HC, Panch SR. Cumulative donor-specific antibody threshold predicts platelet transfusion response in HLA-alloimmunized patients. Blood Adv. 2024 Sep 10;8(17):4689-4699. doi: 10.1182/bloodadvances.2024014143.
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年6月1日
初级完成 (估计的)
2029年1月1日
研究完成 (估计的)
2029年5月31日
研究注册日期
首次提交
2026年6月1日
首先提交符合 QC 标准的
2026年6月7日
首次发布 (实际的)
2026年6月9日
研究记录更新
最后更新发布 (实际的)
2026年6月9日
上次提交的符合 QC 标准的更新
2026年6月7日
最后验证
2026年5月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- XFH2026-05
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
在美国制造并从美国出口的产品
不
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