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高剂量地塞米松序贯泼尼松维持疗法在真实世界中对新诊断的成人免疫性血小板减少症的临床疗效。

Clinical efficacy of high-dose dexamethasone with sequential prednisone maintenance therapy for newly diagnosed adult immune thrombocytopenia in a real-world setting.

作者信息

Xu Jin, Zhang Xinhui, Feng Shanglong, Zhao Na, Hu Xin, Cheng Yaxin, Wu Yue, Zhou Li, Tong Juan, Zheng Changcheng

机构信息

Department of Hematology, Anhui Provincial Hospital, WanNan Medical College, Wuhu, China.

Department of Hematology, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.

出版信息

J Int Med Res. 2021 Apr;49(4):3000605211007322. doi: 10.1177/03000605211007322.

Abstract

OBJECTIVE

As first-line treatments for newly diagnosed adult immune thrombocytopenia (ITP), high-dose dexamethasone (HD-DXM) and conventional-dose prednisone achieve good initial responses, but their long-term efficacy is poor. To improve the long-term outcome of newly diagnosed ITP, we explored the efficacy and safety of HD-DXM with sequential prednisone maintenance therapy.

METHODS

This retrospective study in a real-world setting assessed 72 consecutive newly diagnosed ITP patients administered first-line HD-DXM with sequential prednisone maintenance therapy from 1 June 2016 to 31 December 2019.

RESULTS

Seventy patients obtained response (97.2%), and 55 achieved sustained response (SR) (76.4%). Fifty-three obtained complete remission (CR) (73.6%), and 39 achieved continuous CR at 6 months (54.2%). Among 36 anti-nuclear antibody-positive patients, 100% achieved response, and 28 achieved CR (77.8%). Among 24 antithyroid antibody-positive patients, 23 (95.8%) achieved response, and 20 achieved CR (83.3%). For patients with initial response, the 12-month probability of SR was 78.6%. For patients with initial CR, the 12-month probability of continuous CR was 64.2%. At 12 months, 21.4% of patients with initial response and 11.3% of patients with initial CR showed loss of treatment response.

CONCLUSIONS

HD-DXM with sequential prednisone as the first-line treatment for newly diagnosed ITP patients may achieve good clinical efficacy.

摘要

目的

作为新诊断成人免疫性血小板减少症(ITP)的一线治疗方法,高剂量地塞米松(HD-DXM)和常规剂量泼尼松可取得良好的初始反应,但其长期疗效不佳。为改善新诊断ITP的长期预后,我们探讨了HD-DXM序贯泼尼松维持治疗的疗效和安全性。

方法

这项在真实世界环境中的回顾性研究评估了2016年6月1日至2019年12月31日期间连续接受一线HD-DXM序贯泼尼松维持治疗的72例新诊断ITP患者。

结果

70例患者获得缓解(97.2%),55例达到持续缓解(SR)(76.4%)。53例获得完全缓解(CR)(73.6%),39例在6个月时达到持续CR(54.2%)。在36例抗核抗体阳性患者中,100%获得缓解,28例达到CR(77.8%)。在24例抗甲状腺抗体阳性患者中,23例(95.8%)获得缓解,20例达到CR(83.3%)。对于初始缓解的患者,12个月时SR的概率为78.6%。对于初始CR的患者,12个月时持续CR的概率为64.2%。在12个月时,初始缓解的患者中有21.4%和初始CR的患者中有11.3%出现治疗反应丧失。

结论

HD-DXM序贯泼尼松作为新诊断ITP患者的一线治疗可能取得良好的临床疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd3/8044565/c3d35b1150a1/10.1177_03000605211007322-fig1.jpg

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