Identification factors to adjust early combination regimens in adult primary immune thrombocytopenia: An 8-year data analysis

Kunapa Iam-arunthai, Supat Chamnanchanunt, Pravinwan Thungthong, Chajchawan Nakhahes, T. Suwanban, P. Rojnuckarin
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Abstract

Purpose Recent studies suggested that adding other agents to corticosteroids as a first-line treatment for immune thrombocytopenia (ITP) could improve outcomes. However, combination regimens may increase side effects and costs. To determine clinical factors associated with responses to the first-line steroid at 1 month. Materials and methods We retrospectively reviewed the medical records of patients with ITP aged ≥ 18 years, who were treated at Rajavithi Hospital between 2012 and 2020. Clinical data, laboratory results, treatment regimens, and responses to therapy were analyzed. Results Of the 226 patients, 76.6% were female. The mean age was 46.5 ± 18.1 years, and the median follow-up duration was 40 months. The proportion of chronic ITP was 97.3%. The complete response and response rates to first-line therapy were 65.5% and 88.9%, respectively. The age over 26 years, presentation clinically non-significant bleeding and a difference in platelet count of >50 x 109/L between days 1 and 7 after initial treatment were associated with the response to first-line treatment (adjusted odds ratio [OR] 5.09, 95% confidence interval [CI] 1.50-17.28, p = 0.009); OR 5.87, 95%CI 1.19-28.91, p = 0.029, and OR 3.60, 95%CI 1.10-11.73, p = 0.034, respectively. Younger patients and a difference in platelet count between day 1 and 7 ≤ 50 x 109/L were more likely to require second-line treatments. There were significant increases in the median platelet counts after prescribing azathioprine (baseline vs. 3 months, p = 0.001), cyclophosphamide (baseline vs. 6 months, p = 0.021), or danazol (baseline vs. 12 months, p = 0.039). Conclusion Adult, severity of bleeding at presentation, and rapid platelet increases within 1 week were related to excellent corticosteroid responses in ITP patients. These patients may not need combination regimens.
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调整成人原发性免疫性血小板减少症早期联合方案的识别因素:一项8年数据分析
最近的研究表明,在皮质类固醇的基础上添加其他药物作为治疗免疫性血小板减少症(ITP)的一线治疗可以改善预后。然而,联合用药可能会增加副作用和费用。确定与一线类固醇治疗1个月反应相关的临床因素。材料和方法回顾性分析2012年至2020年在Rajavithi医院治疗的年龄≥18岁的ITP患者的医疗记录。分析了临床资料、实验室结果、治疗方案和对治疗的反应。结果226例患者中,女性占76.6%。平均年龄46.5±18.1岁,中位随访时间40个月。慢性ITP占97.3%。一线治疗的完全缓解率和有效率分别为65.5%和88.9%。年龄大于26岁、出现临床无显著性出血以及初始治疗后第1天至第7天血小板计数>50 × 109/L的差异与一线治疗的疗效相关(校正优势比[OR] 5.09, 95%可信区间[CI] 1.50-17.28, p = 0.009);OR分别为5.87,95%CI 1.19-28.91, p = 0.029; OR为3.60,95%CI 1.10-11.73, p = 0.034。年轻患者和第1天和第7天血小板计数差异≤50 × 109/L的患者更有可能需要二线治疗。在处方硫唑嘌呤(基线vs. 3个月,p = 0.001)、环磷酰胺(基线vs. 6个月,p = 0.021)或那那唑(基线vs. 12个月,p = 0.039)后,血小板计数中位数显著增加。结论成人、就诊时出血严重程度和1周内血小板快速升高与ITP患者良好的皮质类固醇反应有关。这些患者可能不需要联合治疗。
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