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一项回顾性队列研究,监测接受或未接受预处理的急性淋巴细胞白血病患者中聚乙二醇化天冬酰胺酶的活性。

Retrospective cohort study monitoring PEG-asparaginase activity in acute lymphoblastic leukemia patients with and without premedication.

作者信息

Losasso Michael, Bostrom Bruce, Messinger Yoav

机构信息

University of St. Thomas, 2115 Summit Avenue, St. Paul, Minnesota, 55105, USA.

Cancer and Blood Disorders, Children's Minnesota, 2525 Chicago Avenue South, Minneapolis, Minnesota, 55404, USA.

出版信息

F1000Res. 2019 Jul 4;8:1007. doi: 10.12688/f1000research.19298.2. eCollection 2019.

Abstract

PEG-L-asparaginase (pegaspargase) is a critical component of therapy for children and adults with acute lymphoblastic leukemia (ALL). Allergic reactions, which may occur in up to one third of patients, are the major cause for discontinuation. One study reported lower rates of allergic reactions with premedication. Besides allergy, an unknown number of patients develop silent neutralizing antibodies not associated with allergic reactions. The purpose of this retrospective cohort study was to determine the incidence of silent inactivation of pegasparaginase and compare incidence of allergic reactions with and without premedication. Using a commercial assay, asparaginase activity was monitored following pegaspargase (2500 units/m ) in newly diagnosed children and young adults with B- and T-cell ALL from February 2013 to May 2017. The incidence of allergic reactions before and after initiation of premedication in May 2015 was compared. One patient out of 59 (1.7%) had silent inactivation after the second dose. No patient had silent inactivation after the first pegaspargase dose and no standard risk B-cell ALL patients, who received only two pegaspargase doses in combination with oral dexamethasone, had silent inactivation. The incidence of grade 3 or 4 allergic reactions was 3.7% per dose with premedication (methylprednisolone, acetaminophen and diphenhydramine) versus 5.2% without.  The incidence per patient with premedication given for most of the doses was 8.3% versus 17% without. These values are not statistically significant. Premedication did not affect pegaspargase activity. Due to the low incidence of silent inactivation with intravenous pegaspargase and the unlikely event patients receiving only two doses of pegasparaginase would receive erwinase for this possible transient silent inactivation, we recommend routine monitoring of pegaspargase activity only in patients scheduled to receive more than two doses.

摘要

聚乙二醇化左旋门冬酰胺酶(培门冬酶)是治疗儿童和成人急性淋巴细胞白血病(ALL)的关键组成部分。过敏反应在高达三分之一的患者中可能发生,是导致停药的主要原因。一项研究报告称,预处理可降低过敏反应的发生率。除了过敏,还有未知数量的患者会产生与过敏反应无关的无症状中和抗体。这项回顾性队列研究的目的是确定培门冬酶无症状失活的发生率,并比较有无预处理时过敏反应的发生率。使用一种商业检测方法,对2013年2月至2017年5月新诊断的B细胞和T细胞ALL儿童和年轻成人给予培门冬酶(2500单位/m)后监测门冬酰胺酶活性。比较了2015年5月开始预处理前后过敏反应的发生率。59例患者中有1例(1.7%)在第二剂后出现无症状失活。第一剂培门冬酶后没有患者出现无症状失活,并且仅接受两剂培门冬酶联合口服地塞米松的标准风险B细胞ALL患者也没有出现无症状失活。有预处理(甲泼尼龙、对乙酰氨基酚和苯海拉明)时3或4级过敏反应的发生率为每剂3.7%,无预处理时为5.2%。大多数剂量给予预处理的患者中,每位患者的发生率为8.3%,无预处理时为17%。这些值无统计学意义。预处理不影响培门冬酶活性。由于静脉注射培门冬酶无症状失活的发生率较低,且仅接受两剂门冬酰胺酶的患者因这种可能的短暂无症状失活而接受欧文酶的可能性不大,我们建议仅对计划接受超过两剂的患者进行培门冬酶活性的常规监测。

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