[影响 50 岁以上急性髓细胞白血病患者总生存期和预后的因素分析]。

Q4 Medicine
Hong Liu, Zhi Li, Yu-Ye Shi, Shan-Dong Tao, Chun-Ling Wang, Liang Yu
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引用次数: 0

摘要

目的探讨50岁以上急性髓性白血病(AML)患者的总生存率和预后因素:回顾性分析我院2016年1月至2021年6月收治的222例50岁以上急性髓性白血病患者的临床资料。采用Kaplan-Meier法评估总生存率(OS),并采用Cox回归模型评估预后因素:所有患者的1年和3年OS率分别为46.8%和28.8%。随访期间获得缓解的患者的复发率为57%。单变量和多变量分析均显示,高龄、MLL家族融合基因、PHF6基因突变、TP53基因突变、标准化疗不耐受、不完全缓解、复杂核型、+mar核型和inv(3)核型与预后显著相关(所有P AML-ETO融合基因在该人群中没有明显的生存优势)。在完全缓解的患者中,获得最小残留病阴性的患者没有明显的生存优势:结论:50 岁以上的急性髓细胞白血病患者预后差,复发率高。预后受多种因素影响,有其自身的特点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of Factors Influencing Overall Survival and Prognosis of AML Patients Over 50 Years Old].

Objective: To explore the overall survival and prognostic factors of patients over 50 years old with acute myeloid leukemia (AML).

Methods: The clinical data of 222 AML patients aged over 50 years in our hospital from January 2016 and June 2021 were retrospectively analyzed. Kaplan-Meier method was used to evaluate the overall survival (OS) rate, and Cox regression model to evaluate the prognostic factors.

Results: The 1-year and 3-year OS rates of all patients were 46.8% and 28.8%, respectively. The recurrence rate of patients who achieved remission during follow-up time was 57%. Both univariate and multivariate analysis showed that advanced age, MLL family fusion gene, PHF6 gene mutation, TP53 gene mutation, intolerance to standard chemotherapy, incomplete remission, complex karyotype, +mar karyotype and inv(3) karyotype were significantly correlated with prognosis (all P <0.05). Negative fusion gene and positive AML- ETO fusion gene had no obvious survival advantage in this population. In patients with complete remission, there was no significant survival advantage in those who achieved minimal residual disease negative.

Conclusion: AML patients aged over 50 years have a poor outcome and high recurrence rate. The prognosis is affected by multiple factors and has its own characteristics.

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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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