Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Hoxworth Blood Center, Cincinnati, Ohio, USA.
Am J Hematol. 2022 Mar 1;97(3):256-266. doi: 10.1002/ajh.26403. Epub 2021 Dec 23.
Thrombosomes are trehalose-stabilized, freeze-dried group O platelets with a 3-year shelf life. They can be stockpiled, rapidly reconstituted, and infused regardless of the recipient's blood type. Thrombosomes thus represent a potential alternative platelet transfusion strategy. The present study assessed the safety and potential early signals of efficacy of Thrombosomes in bleeding thrombocytopenic patients. We performed an open-label, phase 1 study of single doses of allogeneic Thrombosomes at three dose levels in three cohorts, each consisting of eight patients who had hematologic malignancies, thrombocytopenia, and bleeding. Adverse events, dose-limiting toxicities (DLTs), World Health Organization (WHO) bleeding scores, and hematology values were assessed. No DLTs were reported. The median age was 59 years (24-71). Most patients had AML (58%) or ALL (29%), followed by MDS (8%) and myeloproliferative neoplasm (4%). The WHO scores of 22 patients who were actively bleeding at a total of 27 sites at baseline either improved (n = 17 [63%]) or stabilized (n = 10 [37%]) through day 6. Twenty-four hours after infusion, 12 patients (50%) had a clinically significant platelet count increase. Of eight patients who received no platelet transfusions for 6 days after Thrombosomes infusion, 5 had a clinically significant increase in platelet count of ≥5000 platelets/μL and 2 had platelet count normalization. Thrombosomes doses up to 3.78 × 10 particles/kg demonstrated safety in 24 bleeding, thrombocytopenic patients with hematological malignancies. Thrombosomes may represent an alternative to conventional platelets to treat bleeding. A phase 2 clinical trial in a similar patient population is underway.
血栓体是一种海藻糖稳定的冻干 O 型血小板,具有 3 年的保质期。它们可以储存,快速重建,并输注,无论受者的血型如何。因此,血栓体代表了一种潜在的血小板替代输血策略。本研究评估了在出血性血小板减少症患者中使用血栓体的安全性和潜在早期疗效信号。我们进行了一项开放标签、1 期研究,在三个队列中对三种剂量水平的同种异体血栓体进行了单次剂量研究,每个队列由 8 名患有血液恶性肿瘤、血小板减少和出血的患者组成。评估了不良事件、剂量限制性毒性 (DLT)、世界卫生组织 (WHO) 出血评分和血液学值。未报告 DLT。中位年龄为 59 岁(24-71)。大多数患者患有 AML(58%)或 ALL(29%),其次是 MDS(8%)和骨髓增生性肿瘤(4%)。在基线时有 27 个部位活动性出血的 22 名患者的 WHO 评分通过第 6 天要么改善(n=17 [63%]),要么稳定(n=10 [37%])。输注后 24 小时,12 名患者(50%)血小板计数有临床显著增加。在血栓体输注后 6 天内未接受血小板输注的 8 名患者中,有 5 名患者的血小板计数增加≥5000/μL,2 名患者的血小板计数正常化。在 24 名患有血液恶性肿瘤的出血性血小板减少症患者中,血栓体剂量高达 3.78×10 个颗粒/kg 显示出安全性。血栓体可能是治疗出血的常规血小板的替代方法。一项在类似患者人群中的 2 期临床试验正在进行中。