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Comparison Study between Real Life and Published Data Outcome among Myelofibrosis Patients Who are Using Ruxolitinib at King Abdulaziz Medical City-Central Region

机译:在Abdulaziz国王医学城市中心地区使用Ruxolitinib的霉菌患者现实生活与公布数据结果的比较研究

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Objectives: The aim of this study is to evaluate the efficacy and safety of Ruxolitinib among Myelofibrosis patients in real life compared to published data. Methods: In this retrospective observational chart review study we reviewed the medical records for all patients diagnosed with Myelofibrosis in King Abdulaziz Medical City who has received Ruxolitinib from March 1, 2012-December 1, 2015. The efficacy and safety results of Ruxolitinib were compared with published data. Results: A total of 20 patients were included. The average age was 63.3 (SD=11.6) years, with 55% of females. Efficacy: At week 24, only 20% of the study participant achieved spleen size reduction equal to or more than 20% with total average of 8% reduction in the spleen size as compared to 31.60% in COMFORT-1 study (p <= 0.001), The highest symptoms reduction observed with fatigue and bone pain (45% and 40% of the affected patients respectively) followed by Abdominal distress (35%) whereas no statistically significant difference observed in early satiety and night sweat. Weight loss showed improvement in 15% of the patients. Safety: Fatigue was observed in 45% of the patients, diarrhea (5%), dyspnea (15%), dizziness (5%), nausea (5%), constipation (10%), vomiting (5%), pain in extremities (5%), arthralgia (5%), pyrexia (5%), and abdominal pain (35%). At week 24, Platelet count decreased by 26% and hemoglobin decreased by 5% from the baseline. In general, only three reported cases for temporal or permanent drug discontinuation. Conclusion: Ruxolitinib therapy in real life as compared to published trials was associated with significant improvement in Myelofibrosis related symptoms and splenomegaly with an acceptable safety profile.
机译:目的:本研究的目的是评估ruxolitinib与公布数据相比现实生活中霉菌素患者的疗效和安全性。方法:在此回顾性的观测图表审查研究中,我们审查了在2015年3月1日收到Ruxolitinib的ruxolitinib王的所有患者的医疗记录,这些患者在2015年3月1日起,Ruxolitinib的疗效和安全结果与已发布的数据。结果:共用20名患者。平均年龄为63.3(SD = 11.6)岁,占55%的女性。功效:在第24周,只有20%的研究参与者达到了等于或超过20%的脾脏尺寸减少,脾脏尺寸的总平均值为8%,相比于舒适性1研究的31.60%(P <= 0.001 ),用疲劳和骨痛观察到的最高症状(分别为受影响患者的45%和40%),然后是腹部遇险(35%),而在早期饱腹感和夜间汗液中没有观察到统计学上显着的差异。减肥显示15%的患者的改善。安全性:在45%的患者中观察到疲劳,腹泻(5%),呼吸困难(15%),头晕(5%),恶心(5%),便秘(10%),呕吐(5%),疼痛四肢(5%),关节痛(5%),Pyrexia(5%)和腹痛(35%)。在第24周,血小板计数降低26%,血红蛋白从基线下降5%。一般来说,只有三个报告的颞或永久性药物停止案。结论:与已发表的试验相比,Raxolitinib在现实生活中的治疗与骨髓纤维病相关症状和脾肿大的显着改善有关,具有可接受的安全性。

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