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聚乙二醇化大肠杆菌天冬酰胺酶治疗 NK/T 细胞淋巴瘤患者时对凝血相关不良反应的管理

英文原题:Management of adverse effects associated with pegylated Escherichia coli asparaginase on coagulation in the treatment of patients with NK/T-cell lymphoma.

查看英文原题

Management of adverse effects associated with pegylated Escherichia coli asparaginase on coagulation in the treatment of patients with NK/T-cell lymphoma.

PubMed 2022/03/11(内容时间) Medicine (Baltimore) Q2 · IF 2(JCR 2025)

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中文摘要

自然杀伤/T细胞淋巴瘤(NK/TL)是一种对化疗敏感的疾病,以门冬酰胺酶为基础的化疗已成为该类恶性肿瘤患者近期的标准初始治疗。

本研究旨在评估给予NK/TL患者的聚乙二醇化大肠杆菌(E coli)门冬酰胺酶(PEG-ASP)对凝血的不良反应。回顾性分析2016年1月至2019年12月在中国山西省肿瘤医院血液科接受239个含PEG-ASP化疗周期治疗的71例NK/TL患者(年龄范围13-73岁)的临床资料。按常规时间点获取凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、纤维蛋白原(FBG)和抗凝血酶III(ATIII)数据并进行统计分析。基线第0天(使用PEG-ASP前1天,命名为第0天)的监测参数与第3天(治疗后第3天)至第6天的监测参数之间存在统计学差异,数据表明所有指标均可在21天内恢复。

事件包括PT延长33例(46.5%),APPT延长41例(57.7%,其中20例APTT >60秒),FBG降低49例(69.0%,其中12例FBG <1 g/L),ATIII降低52例(73.2%)。患者平均接受周期数分别为PT(>14秒)2.3个、APTT(>35秒)2.5个、FBG(<2 g/L)2.7个、D-二聚体(>550 ng/mL)2.6个。与第0天相比,PT和APTT在第3天急剧延长(P < .05),在第12天达到峰值,从第3天至第15天维持延长水平,并在第21天逐渐恢复。FBG和ATIII分别在第6天和第3天显著降低(P < .05),两者均在d12降至最低,随后恢复正常。整个治疗过程中D-二聚体水平无显著变化。APTT >60秒或FBG <1 g/L的副作用通过补充新鲜冰冻血浆或冷沉淀输注的对症治疗得到改善,未出现伴随的出血或血栓事件。

我们的数据表明,尽管包含PEG-ASP的化疗对NK/TL患者的凝血功能有中度影响,但定期临床监测是必要的,且大多数NK/TL患者能够成功完成化疗周期。

展开英文摘要原文

Natural killer/T-cell lymphoma (NK/TL) is a chemotherapy-sensitive disease, and asparaginase-based chemotherapy has become the standard primary treatment for patients with this malignancy recently. The objective of this study was to evaluate the adverse reactions on blood coagulation of the administered pegylated Escherichia coli (E coli) asparaginase (PEG-ASP) to the NK/TL patients. Clinical data of 71 NK/TL patients (range 13-73 years), who received 239 cycles of chemotherapy treatment containing PEG-ASP in the Hematology Department of Shanxi Province Cancer Hospital of China from January 2016 to December 2019 were analyzed retrospectively. Data of prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen (FBG), and antithrombinIII (ATIII) were obtained at the time points routinely and statistically analyzed. There were statistical differences between the monitored parameters of baseline day0 (the day before use of PEG-ASP, named day0) and those of day3 (the 3rd day after treatment) to day6, and data showed all of the indicators could recover within 21 days.

The events included PT prolonged in 33 patients (46. 5%), APPT prolonged in 41 patients (57. 7%, 20 patients with APTT >60 seconds), FBG decreased in 49 patients (69. 0%, 12 patients with FBG <1 g/L), and ATIII decreased in 52 patients (73. 2%). The patients' average number of cycles received was 2. 3 for PT (>14 seconds), 2. 5 for APTT (>35 seconds), 2. 7 for FBG (<2 g/L), and 2. 6 for D-dimer (>550 ng/mL). Compared with those at day0, PT and APTT prolonged sharply at day3 (P < .

05), reached the peak at day12, maintained the prolonged level from day3 to day15, and gradually recovered at day 21. FBG and ATIII significantly decreased at day6 and day3 respectively (P < . 05), both of them fell to the minimum at day12, and then returned the normal.

The D-dimer levels were no significantly change during the whole treatment course. The APTT >60 seconds or FBG <1 g/L side effects were improved by symptomatic treatment of supplementation of fresh frozen plasma or cryoprecipitate infusion, no concomitant bleeding or thrombotic events emerging.

Our data suggested although chemotherapy including PEG-ASP impacted moderately on the coagulation function of NK/TL patients, clinically monitored regularly were necessary and most NK/TL patients can complete the chemotherapy cycles successfully.

论文信息

作者
Yang J、Guo X、Guo S、Yan H、Chai L、Guo Y、Li Z、Hao Z
第一作者单位
Department of Pharmacy, Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, PR China.China
通讯作者单位
Department of Hematology, Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, PR China.China
期刊
Medicine2022 Mar 11
原文标识
PubMed 35451376 · DOI 10.1097/MD.0000000000025578