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2023年急性早幼粒细胞白血病的治疗:模式、进展与未来方向。

The treatment of acute promyelocytic leukemia in 2023: Paradigm, advances, and future directions.

作者信息

Iyer Sunil Girish, Elias Laila, Stanchina Michele, Watts Justin

机构信息

Department of Medicine, Division of Hematology, University of Miami Miller School of Medicine, Miami, FL, United States.

Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, United States.

出版信息

Front Oncol. 2023 Jan 18;12:1062524. doi: 10.3389/fonc.2022.1062524. eCollection 2022.

Abstract

The transformation of acute promyelocytic leukemia (APL) from an often fatal to highly curable cancer with long-term survival exceeding 90% is one of the greatest and most inspiring successes in oncology. A deeper understanding of the pathogenesis of APL heralded the introduction of highly effective therapies targeting the mutant protein that drives the disease, leading to the chemotherapy-free approach to cure almost all patients. In this review, we discuss the paradigm of treatment of APL in 2023, reinforce the high risk of early death without prompt initiation of treatment at first clinical suspicion, and dedicate a special focus to novel agents and future directions to improve cure rates and quality of life in patients affected by APL.

摘要

急性早幼粒细胞白血病(APL)从一种通常致命的癌症转变为治愈率极高、长期生存率超过90%的癌症,这是肿瘤学领域最伟大、最鼓舞人心的成功之一。对APL发病机制的深入理解促成了针对驱动该疾病的突变蛋白的高效疗法的引入,从而形成了几乎能治愈所有患者的无化疗治疗方法。在本综述中,我们讨论了2023年APL的治疗模式,强调了在首次临床怀疑时不立即开始治疗会导致早期死亡的高风险,并特别关注新型药物以及提高APL患者治愈率和生活质量的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee0/9889825/a3d5cb1b441e/fonc-12-1062524-g001.jpg

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