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          其临床症状、缩小脾脏。血小板计数<50×10  L 不应                            髓纤维化的有效性和安全性[J]. 青岛大学学报(医学
          视为芦可替尼治疗的绝对禁忌证,临床上可根据患者的                                版),2025,61(1):29-33.
          情况评估风险与收益,在患者知情同意下,试行芦可替                           [12]  US Department of Health and Human Services,National
          尼治疗 。但鉴于本研究仅纳入2例血小板计数<50×                               Institutes  of  Health,National  Cancer  Institute. Common
                [11]
                                                                  Terminology Criteria for Adverse Events(CTCAE),ver‐
              -1
          10  L 的患者,尚需扩大样本量进一步证实。
            9
              综上所述,芦可替尼能有效改善 MF 患者的临床症                            sion 4.03[EB/OL]. [2024-12-01].http://www.eortc.be/ser‐
                                                                  vices/doc/ctc/ctcae_4.03_2010-06-14_quickreference_5x7.
          状,缩小脾脏,稳定甚至改善 MF 分级,有望为 MF 患者
                                                                  pdf.
          带来长期生存获益;ADR主要为贫血、血小板减少、感染                         [13]  WHO.The use of the WHO-UMC system for standardised
          及胃肠道不适。本研究的局限性为:(1)本文为单中心                               case causality assessment[EB/OL]. [2024-12-02]. https://
          回顾性研究,纳入的样本量较少,随访时间较短,结果可                               www.who.int/publications/m/item/WHO-causality-assess-
          能存在一定偏倚;(2)由于芦可替尼作为MF一线治疗的                              ment.
          疗效数据已明确,且有研究以单药芦可替尼的脾脏反应                           [14]  KVASNICKA H M,THIELE J,BUESO-RAMOS C E,et
          率、生存期为参照       [9,15,17] ,所以本研究未设置对照组。因                 al.  Long-term  effects  of  ruxolitinib  versus  best  available
          此,本文所得结论尚需更多大样本(尤其是纳入血小板                                therapy on bone marrow fibrosis in patients with myelofi‐
          计数<50×10  L 患者)、多中心对照研究进一步证实。                           brosis[J]. J Hematol Oncol,2018,11(1):42.
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          中国药房  2025年第36卷第14期                                              China Pharmacy  2025 Vol. 36  No. 14    · 1785 ·
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