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接受天冬酰胺酶治疗的血液系统恶性肿瘤成年患者采用较低抗凝血酶替代目标的安全性和可行性

Safety and feasibility of lower antithrombin replacement targets in adult patients with hematological malignancies receiving asparaginase therapy<sup/>.

作者信息

Barreto Jason N, McCullough Kristen B, Peskey Candy S, Dierkhising Ross A, Mara Kristin C, Elliott Michelle A, Gastineau Dennis A, Al-Kali Aref, Gangat Naseema, Letendre Louis, Hogan William J, Litzow Mark R, Patnaik Mrinal M

机构信息

a Department of Pharmacy Services , Mayo Clinic , Rochester , MN , USA.

b Division of Biomedical Statistics and Informatics, Department of Health Sciences Research , Mayo Clinic , Rochester , MN , USA.

出版信息

Leuk Lymphoma. 2017 Nov;58(11):2588-2597. doi: 10.1080/10428194.2017.1312384. Epub 2017 May 9.

Abstract

The optimal antithrombin(AT) activity parameters for replacement as thromboprophylaxis following asparaginase remains unclear. This single-center, retrospective study evaluated two sets of AT replacement thresholds and targets in adults receiving asparaginase-containing chemotherapy. AT supplementation adhered to institutional standards, which lowered the AT activity target from 100% to 80% in 6/2014. Ninety-two patients were evaluated. Cumulative thrombosis incidence was 16% at 6 months (95%CI:6.8-24.0, maximum follow-up 315 days) with similar incidence between the 80% and 100% target groups, 14% (2 of the 14) and 13% (10 of the 78), respectively, with a small non-Line-Related DVT incidence (3%). Most thrombotic events occurred during induction chemotherapy and demonstrated no associations with replacement target, cumulative days or cumulative area under AT activity target, number of asparaginase doses, or cumulative asparaginase dose. Median estimated AT replacement expenditure was $34,963USD (IQR $16,260USD to $79,319USD) per patient. Cost-effectiveness and optimization of AT replacement for thromboprophylaxis following asparaginase requires prospective evaluation.

摘要

门冬酰胺酶治疗后作为血栓预防替代治疗的最佳抗凝血酶(AT)活性参数仍不清楚。这项单中心回顾性研究评估了接受含门冬酰胺酶化疗的成人患者的两组AT替代阈值和目标。AT补充遵循机构标准,该标准在2014年6月将AT活性目标从100%降至80%。共评估了92例患者。6个月时累积血栓形成发生率为16%(95%CI:6.8-24.0,最长随访315天),80%和100%目标组的发生率相似,分别为14%(14例中的2例)和13%(78例中的10例),非线性相关的深静脉血栓形成发生率较低(3%)。大多数血栓形成事件发生在诱导化疗期间,且与替代目标、累积天数或AT活性目标下的累积面积、门冬酰胺酶剂量数或累积门冬酰胺酶剂量无关。每位患者的AT替代估计中位费用为34,963美元(IQR 16,260美元至79,319美元)。门冬酰胺酶治疗后用于血栓预防的AT替代的成本效益和优化需要前瞻性评估。

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