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PICALM-MLLT10 融合基因在血液肿瘤中的临床特征、当前实践及预后

英文原题:PICALM-MLLT10 fusion gene in hematological neoplasms: clinical features, current practices, and prognoses.

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PICALM-MLLT10 fusion gene in hematological neoplasms: clinical features, current practices, and prognoses.

PubMed 2024/11/05(内容时间) Hematology Q3 · IF 2(JCR 2025)

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研究概要

PLCALM-MALLT10 患者可诊断为 AML、ALL、MPAL 及其他极为罕见的血液系统恶性肿瘤,临床表现混合,生存率低。未来可考虑新型强化治疗,包括造血干细胞移植、CAR-T 细胞免疫治疗以及靶向药物如 Bcl-2 抑制剂。

研究思路结论见上方概要

PICALM-MLLT10,曾用名CALM-AF10,是一种在血液系统恶性肿瘤中罕见报道的融合基因,尤其在亚洲人群中。病例介绍:2019年10月至2023年10月期间,在中国浙江大学医学院附属第一医院共鉴定出6例携带PICALM-MALLT10融合基因的患者,中位年龄为25岁。临床诊断包括急性髓系白血病(AML)2例、急性淋巴细胞白血病(ALL)3例、混合表型急性白血病(MPAL)1例。患者预后较差,尽管接受了强化治疗,仍有3例患者在1年内死亡。

展开英文摘要原文

INTRODUCTION: PICALM - MLLT10 , formerly CALM-AF10 , is a rarely reported fusion gene in hematological malignancies, especially in Asian people. CASE PRESENTATIONS: Six patients with PICALM-MALLT10 fusion gene were identified at the First Affiliated Hospital, Zhejiang University School of Medicine, China between October 2019 and October 2023, with a median age of 25 years. Clinical diagnoses included acute myeloid leukemia (AML) in 2 patients, acute lymphoblastic leukemia (ALL) in 3, and mixed phenotype acute leukemia (MPAL) in 1. The prognosis of the patients was poor, and three patients died within 1 year despite of intensive treatment. CONCLUSION: Patients with PLCALM-MALLT10 can be diagnosed as AML, ALL, MPAL, and other extremely rare hematological malignancies, with mixed clinical manifestations and poor survival. Novel and intensive therapies, including hematopoietic stem cell transplantation, chimeric antigen receptor T-cell immunotherapy, and targeted agents such as the Bcl-2 inhibitor, could be considered in the future.

论文信息

作者
Wang JN、Ye B、Cheng F、Yang L、Hu Y、Zheng G、Cai Z、Yu J
单位
Bone Marrow Transplantation Center of The First Affiliated Hospital & Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.China
文献类型
病例报告
期刊
Hematology (Amsterdam, Netherlands)2024 Dec
原文标识
PubMed 39499083 · DOI 10.1080/16078454.2024.2423324