Maladies du Sang, Centre Hospitalier Universitaire (CHU) d'Angers, Angers, France.
Fédération Hospitalo-Universitaire Grand-Ouest Acute Leukemia (FHU-GOAL), Angers, France.
Blood. 2020 Jul 16;136(3):328-338. doi: 10.1182/blood.2020004919.
Patients undergoing treatment of acute lymphoblastic leukemia (ALL) are at risk for thrombosis, caused in part by the use of l-asparaginase (L-ASP). Antithrombin (AT) replacement has been suggested to prevent venous thromboembolism (VTE) and thus may increase exposure to ASP. We report herein the results of the prophylactic replacement strategy in the pediatrics-inspired prospective GRAALL-2005 study. Between 2006 and 2014, 784 adult patients with newly diagnosed Philadelphia- ALL were included. The incidence rate of VTE was 16%, with 69% of cases occurring during induction therapy. Most patients received AT supplementation (87%). After excluding patients who did not receive L-ASP or who developed thrombosis before L-ASP, AT supplementation did not have a significant impact on VTE. Administration of fibrinogen concentrates was associated with an increased risk of VTE, whereas transfusion of fresh frozen plasma had no effect. Heparin prophylaxis was associated with an increased risk of VTE. Prophylactic measures were not associated with an increased risk of grade 3 to 4 bleeding complications. The rate of VTE recurrence after L-ASP reintroduction was 3% (1 of 34). In ALL patients receiving L-ASP therapy, the use of fibrinogen concentrates may increase the risk of thrombosis and should be restricted to rare patients with hypofibrinogenemia-induced hemorrhage. VTE developed despite extensive AT supplementation, which suggests the need for additional prophylactic measures. Although this large descriptive study was not powered to demonstrate the efficacy of these prophylactic measures, it provides important insight to guide future trial design. This trial was registered at www.clinicaltrials.gov as #NCT00327678.
接受急性淋巴细胞白血病 (ALL) 治疗的患者存在血栓形成的风险,部分原因是使用 L-天冬酰胺酶 (L-ASP)。已建议使用抗凝血酶 (AT) 替代物来预防静脉血栓栓塞症 (VTE),从而可能增加 ASP 的暴露。我们在此报告了在儿科启发的前瞻性 GRAALL-2005 研究中预防性替代策略的结果。在 2006 年至 2014 年期间,纳入了 784 名新诊断为费城 ALL 的成年患者。VTE 的发生率为 16%,其中 69%的病例发生在诱导治疗期间。大多数患者接受了 AT 补充治疗(87%)。在排除未接受 L-ASP 或在接受 L-ASP 之前发生血栓形成的患者后,AT 补充治疗对 VTE 没有显著影响。纤维蛋白原浓缩物的给药与 VTE 风险增加相关,而新鲜冷冻血浆的输血则没有影响。肝素预防与 VTE 风险增加相关。预防性措施与 3 级至 4 级出血并发症的风险增加无关。在重新引入 L-ASP 后,VTE 复发的发生率为 3%(34 例中的 1 例)。在接受 L-ASP 治疗的 ALL 患者中,纤维蛋白原浓缩物的使用可能会增加血栓形成的风险,并且应仅限于因低纤维蛋白原血症引起的出血而罕见的患者。尽管广泛使用了 AT 补充治疗,但仍发生了 VTE,这表明需要采取额外的预防措施。尽管这项大型描述性研究没有能力证明这些预防措施的疗效,但它为指导未来的试验设计提供了重要的见解。该试验在 www.clinicaltrials.gov 上注册为 #NCT00327678。