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Pretreatment Absolute Immature Platelet Count is a Promising Predictor of Response to Short-Term Dexamethasone Monotherapy or Combination Therapy in Newly Diagnosed Adult Primary Immune Thrombocytopenia
Indian Journal of Hematology and Blood Transfusion ( IF 0.9 ) Pub Date : 2023-10-20 , DOI: 10.1007/s12288-023-01702-w
Mengen lv , Qing Xu , Xianfei Ye , Qian Yu , Bibin Wang , Ying Wang

Reliable indicators that can predict drug responsiveness in primary immune thrombocytopenia (ITP) patients are urgent. We aimed to establish a reference interval of percentage of immature platelet fraction (IPF%) and absolute immature platelet count (A-IPC), and assess their efficacy in discriminating ITP patients from controls, especially their predictive value for responsiveness to drug treatment. We retrospectively studied 72 treatment-naive adult patients with ITP who received Dexamethasone monotherapy or combination therapy. Baseline (pretreatment) information was collected from medical records. Reference intervals for A-IPC and IPF% were established based on controls and their effectiveness in discriminating ITP patients from controls was assessed. Predictive value of pretreatment IPF% and A-IPC at four co-primary endpoints of treatment response in patients were investigated. The 95% reference intervals for A-IPC and IPF% were (2.7–15.6) × 109/L and 1.2%–7.3%, respectively. Both A-IPC and IPF% had excellent discrimination ability for ITP patients from controls. It showed highly statistically significant differences in pretreatment A-IPC for predicting treatment response at day 7 between responders and non-responders, but not at days 14, 21 and 28. Pretreatment A-IPC had the higher area under the ROC curve with a cut-off of 0.86 than that of IPF% with a cut-off of 14.5% in predicting the treatment response in ITP patients at day 7. Pretreatment A-IPC exhibited acceptable predictive power and could be a promising predictor of response to short-term Dexamethasone monotherapy or combination therapy at day 7 in ITP patients.



中文翻译:

治疗前绝对未成熟血小板计数是新诊断成人原发性免疫性血小板减少症短期地塞米松单药治疗或联合治疗反应的有希望的预测因子

迫切需要能够预测原发性免疫性血小板减少症(ITP)患者药物反应的可靠指标。我们的目的是建立未成熟血小板分数百分比 (IPF%) 和绝对未成熟血小板计数 (A-IPC) 的参考区间,并评估其区分 ITP 患者与对照组的功效,特别是其对药物治疗反应的预测价值。我们回顾性研究了 72 名接受过地塞米松单药治疗或联合治疗的初治成人 ITP 患者。从医疗记录中收集基线(治疗前)信息。A-IPC 和 IPF% 的参考区间是根据对照建立的,并评估了它们区分 ITP 患者和对照的有效性。研究了治疗前 IPF% 和 A-IPC 在患者治疗反应的四个共同主要终点上的预测价值。A-IPC 和 IPF% 的 95% 参考区间分别为 (2.7–15.6) × 10 9 /L 和 1.2%–7.3%。A-IPC 和 IPF% 对 ITP 患者与对照组均具有出色的区分能力。结果显示,治疗前 A-IPC 在预测第 7 天有反应者和无反应者的治疗反应方面存在高度统计学显着差异,但在第 14、21 和 28 天则没有差异。治疗前 A-IPC 的 ROC 曲线下面积较高,且有切口在预测第 7 天 ITP 患者的治疗反应时,与 IPF% 相比,截断值为 0.86,截断值为 14.5%。治疗前 A-IPC 表现出可接受的预测能力,可能是短期地塞米松反应的有希望的预测因子ITP 患者在第 7 天进行单一疗法或联合疗法。

更新日期:2023-10-20
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