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芦可替尼与最佳可用疗法治疗原发性骨髓纤维化的疗效评价。

Evaluation of Ruxolitinib versus Best Available Therapy in Treating Primary Myelofibrosis.

机构信息

Department of Medicine, Erbil, Iraq.

Nanakali Hospital for Blood Diseases and Oncology, Erbil, Iraq.

出版信息

Sultan Qaboos Univ Med J. 2022 Aug;22(3):393-399. doi: 10.18295/squmj.8.2021.110. Epub 2022 Aug 25.

Abstract

OBJECTIVES

This study aimed to evaluate the effectiveness of ruxolitinib and compare it with the best available therapy in patients with primary myelofibrosis. Ruxolitinib is a Janus kinase inhibitor that is approved for the treatment of myelofibrosis. The therapeutic protocol has changed after the introduction of ruxolitinib.

METHODS

In this retrospective study, 72 patients with primary myelofibrosis were scrutinised from January 2012 to January 2018 at Nanakali Hemato-Oncology Teaching Centre in Erbil, Iraqi Kurdistan. The patients were divided into two cohorts: 26 of them were treated with ruxolitinib and 46 received the best available therapy. The patients' characteristics, their response to the treatment and the outcomes were evaluated. The efficacy of the treatment in both groups was compared.

RESULTS

Most patients (n = 46; 63.9%) were in the high and intermediate-2 risk groups according to the international prognostic scoring system. At the time of diagnosis, no noticeable differences in the clinical characteristics and laboratory data were observed among the ruxolitinib and best available treatment groups. Ruxolitinib was found to be effective in reducing the size of the spleen and improving the overall survival rate when compared to the best available treatment group ( <0.001 and = 0.008, respectively). The patients' performance status had a significant effect on the overall survival in both treatment groups ( = 0.003).

CONCLUSION

Ruxolitinib appears to have a significant role in reducing the spleen size and potentially affect the survival outcomes in patients with myelofibrosis.

摘要

目的

本研究旨在评估芦可替尼的疗效,并将其与原发性骨髓纤维化患者的最佳可用疗法进行比较。芦可替尼是一种已被批准用于治疗骨髓纤维化的 Janus 激酶抑制剂。在芦可替尼问世后,治疗方案发生了变化。

方法

在这项回顾性研究中,我们对 2012 年 1 月至 2018 年 1 月在伊拉克库尔德斯坦埃尔比勒的 Nanakali 血液肿瘤学教学中心的 72 名原发性骨髓纤维化患者进行了研究。患者被分为两组:26 名患者接受芦可替尼治疗,46 名患者接受最佳可用疗法。评估了患者的特征、对治疗的反应和结局。比较了两组的治疗效果。

结果

根据国际预后评分系统,大多数患者(n=46;63.9%)处于高风险和中-2 风险组。在诊断时,芦可替尼组和最佳可用治疗组在临床特征和实验室数据方面没有明显差异。与最佳可用治疗组相比,芦可替尼可有效降低脾脏大小并提高总生存率(<0.001 和=0.008)。在两组中,患者的体能状态对总生存率均有显著影响(=0.003)。

结论

芦可替尼似乎在降低脾脏大小和潜在影响骨髓纤维化患者的生存结果方面具有重要作用。

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