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靶向治疗在儿科急性淋巴细胞白血病治疗中的应用——治疗机制与毒性机制。

Targeted Therapy in the Treatment of Pediatric Acute Lymphoblastic Leukemia-Therapy and Toxicity Mechanisms.

机构信息

Laboratory of Genetic Diagnostics, Medical University of Lublin, A. Gębali 6, 20-093 Lublin, Poland.

Student Scientific Society, Laboratory of Genetic Diagnostics, Medical University of Lublin, A. Gębali 6, 20-093 Lublin, Poland.

出版信息

Int J Mol Sci. 2021 Sep 11;22(18):9827. doi: 10.3390/ijms22189827.

Abstract

Targeted therapy has revolutionized the treatment of poor-prognosis pediatric acute lymphoblastic leukemia (ALL) with specific genetic abnormalities. It is still being described as a new landmark therapeutic approach. The main purpose of the use of molecularly targeted drugs and immunotherapy in the treatment of ALL is to improve the treatment outcomes and reduce the doses of conventional chemotherapy, while maintaining the effectiveness of the therapy. Despite promising treatment results, there is limited clinical research on the effect of target cell therapy on the potential toxic events in children and adolescents. The recent development of highly specific molecular methods has led to an improvement in the identification of numerous unique expression profiles of acute lymphoblastic leukemia. The detection of specific genetic mutations determines patients' risk groups, which allows for patient stratification and for an adjustment of the directed and personalized target therapies that are focused on particular molecular alteration. This review summarizes the knowledge concerning the toxicity of molecular-targeted drugs and immunotherapies applied in childhood ALL.

摘要

靶向治疗已彻底改变了具有特定遗传异常的预后不良的儿科急性淋巴细胞白血病(ALL)的治疗方法,被认为是一种新的治疗方法。在 ALL 的治疗中使用分子靶向药物和免疫疗法的主要目的是提高治疗效果并降低常规化疗的剂量,同时保持治疗的有效性。尽管治疗结果令人鼓舞,但针对靶向细胞治疗对儿童和青少年潜在毒性事件的影响的临床研究有限。最近高度特异性分子方法的发展导致了对急性淋巴细胞白血病的许多独特表达谱的识别得到了改善。特定基因突变的检测确定了患者的危险组,这允许对患者进行分层,并对针对特定分子改变的定向和个性化靶向治疗进行调整。本文综述了有关应用于儿童 ALL 的分子靶向药物和免疫疗法的毒性的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b819/8468873/49850cd65b09/ijms-22-09827-g001.jpg

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