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在巩固化疗后骨髓抑制期间,利奈唑胺对 AML 患者的血小板计数是安全的。

Linezolid is safe on platelet count for AML patients during myelosuppression after consolidation chemotherapy.

机构信息

Department of Hematology, The First Affiliated Hospital, Zhejiang University College of Medicine, Hangzhou, P.R. China.

出版信息

J Clin Pharm Ther. 2020 Aug;45(4):755-758. doi: 10.1111/jcpt.13159. Epub 2020 May 13.

DOI:10.1111/jcpt.13159
PMID:32403181
Abstract

BACKGROUND

Patients with acute myeloid leukaemia (AML) often develop severe infections during myelosuppression after chemotherapy. Linezolid is an appropriate choice for these patients when coverage of positive bacteria is needed. An important side effect of linezolid is linezolid-induced thrombocytopenia; so, the safety of linezolid for AML patients in myelosuppression is of concern. No study has focused on platelets in these patients.

METHODS

We reviewed 1356 AML patients who received consolidation chemotherapy in our hospital during January 2009 and June 2019. Among them, 36 patients were treated with linezolid and 41 with vancomycin. We counted the days of platelet count <2010E9/L, <5010E9/L, the lowest platelet count, total quantity of platelet transfusion and clinical bleeding events of these patients, to evaluate the safety of linezolid during myelosuppression in AML patients.

RESULTS

The days of platelet count <2010E9/L in the linezolid group and vancomycin group were 6.2 ± 2.5 days and 6.7 ± 2.9 days, and the days of platelet count <5010E9/L in the linezolid group and vancomycin group were 10.9 ± 3.6 days and 11.7 ± 4.0 days, respectively; there was no significant difference between the two groups. No life-threatening severe bleeding events occurred in either group.

CONCLUSION

This retrospective clinical study suggests that it is safe to manage AML patients in complete remission during myelosuppression after standard consolidation chemotherapy with idarubicin and cytarabine, with about 7 days of linezolid therapy.

摘要

背景

急性髓系白血病(AML)患者在化疗后骨髓抑制期间常发生严重感染。当需要覆盖阳性菌时,利奈唑胺是这些患者的合适选择。利奈唑胺的一个重要副作用是利奈唑胺引起的血小板减少症;因此,骨髓抑制期间 AML 患者使用利奈唑胺的安全性令人关注。没有研究关注这些患者的血小板。

方法

我们回顾了 2009 年 1 月至 2019 年 6 月期间在我院接受巩固化疗的 1356 例 AML 患者。其中 36 例患者接受利奈唑胺治疗,41 例患者接受万古霉素治疗。我们计算了血小板计数<20×10E9/L、<50×10E9/L、血小板计数最低、血小板输注总量和这些患者的临床出血事件的天数,以评估 AML 患者骨髓抑制期间利奈唑胺的安全性。

结果

利奈唑胺组和万古霉素组血小板计数<20×10E9/L 的天数分别为 6.2±2.5 天和 6.7±2.9 天,血小板计数<50×10E9/L 的天数分别为 10.9±3.6 天和 11.7±4.0 天,两组之间无显著差异。两组均未发生危及生命的严重出血事件。

结论

这项回顾性临床研究表明,在标准阿糖胞苷和柔红霉素巩固化疗后骨髓抑制期间,使用利奈唑胺治疗 AML 患者完全缓解是安全的,约 7 天即可完成治疗。

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