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携带RUNX1突变的急性髓系白血病患者的临床结局:它仍然是不良预后因素吗?一项队列研究和荟萃分析。

Clinical Outcomes of Acute Myeloid Leukemia Patients Harboring the RUNX1 Mutation: Is It Still an Unfavorable Prognosis? A Cohort Study and Meta-Analysis.

作者信息

Rungjirajittranon Tarinee, Siriwannangkul Theerapat, Kungwankiattichai Smith, Leelakanok Nattawut, Rotchanapanya Wannaphorn, Vittayawacharin Pongthep, Mekrakseree Benjamaporn, Kulchutisin Kamolchanok, Owattanapanich Weerapat

机构信息

Division of Hematology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.

Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Burapha University, Chonburi 20131, Thailand.

出版信息

Cancers (Basel). 2022 Oct 26;14(21):5239. doi: 10.3390/cancers14215239.

Abstract

Acute myeloid leukemia (AML) with mutated () is considered to have an unfavorable prognosis. However, recent studies have reported comparable survival outcomes with wild-type (). To assess the clinical outcomes of AML with and without , we performed a prospective cohort study and systematic review and meta-analysis. The study enrolled 135 patients (27 with ; 108 with ). There were no significant differences in the median OS and RFS of the and groups (9.1 vs. 12.2 months; = 0.268 and 7.8 vs. 14.6 months; = 0.481, respectively). A subgroup analysis of AML patients with intermediate-risk cytogenetics showed similar outcomes. Our meta-analysis pooled data from 23 studies and our study. The complete remission rate was significantly lower in the group (pooled odds ratio: 0.42). The OS, RFS, and event-free survival rates also favored the group (pooled risk ratios: 1.36, 1.37, and 1.37, respectively). A subgroup analysis of AML patients with intermediate-risk cytogenetics demonstrated nearly identical OS and RFS outcomes. This study confirms that patients with AML and had poor prognoses. Nonetheless, in AML with intermediate-risk cytogenetics, the survival outcomes of both groups were comparable.

摘要

伴有 () 突变的急性髓系白血病(AML)被认为预后不良。然而,最近的研究报告了其与野生型 () 具有相似的生存结果。为了评估伴有和不伴有 的AML患者的临床结局,我们进行了一项前瞻性队列研究以及系统评价和荟萃分析。该研究纳入了135例患者(27例伴有 ;108例伴有 )。伴有 和不伴有 的两组患者的中位总生存期(OS)和无复发生存期(RFS)无显著差异(分别为9.1个月对12.2个月;P = 0.268以及7.8个月对14.6个月;P = 0.481)。对具有中危细胞遗传学特征的AML患者进行的亚组分析显示了相似的结果。我们的荟萃分析汇总了来自23项研究以及我们这项研究的数据。伴有 的组完全缓解率显著更低(合并比值比:0.42)。总生存期、无复发生存期和无事件生存率也更有利于不伴有 的组(合并风险比分别为:1.36、1.37和1.37)。对具有中危细胞遗传学特征的AML患者进行的亚组分析显示总生存期和无复发生存期结果几乎相同。本研究证实伴有 的AML患者预后较差。尽管如此,在具有中危细胞遗传学特征的AML中,两组的生存结果具有可比性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3edb/9659296/8f957126e5ae/cancers-14-05239-g001.jpg

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