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TP53 突变的急性髓系白血病:我们如何改善治疗结果?

TP53-mutated acute myeloid leukemia: how can we improve outcomes?

作者信息

Sallman David A, Stahl Maximilian

机构信息

Malignant Hematology Department, Moffitt Cancer Center, Tampa, FL.

Division of Leukemia, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.

出版信息

Blood. 2025 Jun 12;145(24):2828-2833. doi: 10.1182/blood.2024024245.

Abstract

Despite advances in the treatment paradigm of patients with acute myeloid leukemia (AML), TP53-mutated AML represents a molecular subgroup that has failed to improve, with an overall survival of ∼6 months that is independent of age and fitness. Notably, there has been significant elucidation in understanding the biology of the disease and key advancements in the classification and prognostication of these patients. International collaborative efforts for novel clinical interventions are urgently needed to change the standard of care.

摘要

尽管急性髓系白血病(AML)患者的治疗模式取得了进展,但TP53突变的AML代表了一个未能得到改善的分子亚组,其总生存期约为6个月,与年龄和健康状况无关。值得注意的是,在了解该疾病的生物学特性以及这些患者的分类和预后方面已经有了重大进展。迫切需要开展国际合作以进行新的临床干预,从而改变治疗标准。

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