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本次评估受限于临床试验数量较少及泽布替尼上 [ 6 ] 嵇承栋,朱琳懿,万悦竹,等. 国际卫生技术评估机构协
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数量。由于纳入的 RCT 在患者人群和结局指标上存在 porting checklist of health technology assessment deve-
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technology assessment[J]. Chin J Evid Based Med,2016,
疗效及安全性数据。经济学研究结果受到多个因素的
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影响,如药品价格、评估角度、患者群体和意愿支付阈值
[ 7 ] HILLMEN P,EICHHORST B,BROWN J R,et al. Zanu‐
等,目前尚无法明确泽布替尼的经济学优势。未来研究
brutinib versus ibrutinib in relapsed/refractory chronic
应纳入更多中国患者数据,长期监测泽布替尼的疗效和 lymphocytic leukemia and small lymphocytic lymphoma:
安全性。随着更多高质量的临床研究和系统评价的出 interim analysis of a randomized phase Ⅲ trial[J]. J Clin
现,后续对泽布替尼的评估将更全面、可靠。 Oncol,2023,41(5):1035-1045.
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现出良好的有效性和安全性,同时对于R/R MCL患者具 brutinib or ibrutinib in relapsed or refractory chronic lym‐
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应用前景。随着研究的不断深入、适应证范围的扩大及
lymphocytic leukaemia and small lymphocytic lymphoma
真实世界应用的推广,泽布替尼有望为更多患者带来
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