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急性白血病治疗中的一个难题:谱系转换。

A shadow in the treatment of acute leukemia: lineage switch.

作者信息

Zhou Qiaoyi, Wang Ying

机构信息

State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.

Tianjin Institutes of Health Science, Tianjin 301600, China.

出版信息

Blood Sci. 2025 Mar 20;7(2):e00220. doi: 10.1097/BS9.0000000000000220. eCollection 2025 Jun.

Abstract

Lineage switch is a rare phenomenon in which acute myeloid leukemia (AML) transforms into acute lymphoblastic leukemia (ALL) and vice versa, sharing the same clonal origin. It is more common for AML to relapse as ALL. Cytogenetics, microenvironment, and preceding therapies are associated with lineage switch. Since the etiology of lineage switch is unclear, presumptions include clonal selection, pluripotent stem cells, and differentiated cell trans-differentiation or re-differentiation. The key point for diagnosing lineage switch is that the relapsed tumor originates from the common cell of the primary leukemia, although it is occasionally derived via clonal evolution. It is very important to distinguish lineage switch from other illnesses, such as secondary leukemia or the blast phase of chronic leukemia. Although direct treatment of the present lineage results in an improved prognosis, the outcome of these patients remains poor, with low survival and rapid progression. Hematopoietic stem cell transplantation can extend survival. Lineage switch risk-adapted management stratification may be beneficial for detecting relapse and more promptly provide suitable therapy. Efficient and toxicity-restricted therapy is being developed to improve the very poor prognosis.

摘要

谱系转换是一种罕见的现象,即急性髓系白血病(AML)转变为急性淋巴细胞白血病(ALL),反之亦然,两者具有相同的克隆起源。AML复发为ALL更为常见。细胞遗传学、微环境和先前的治疗与谱系转换有关。由于谱系转换的病因尚不清楚,推测包括克隆选择、多能干细胞以及分化细胞的转分化或再分化。诊断谱系转换的关键在于复发肿瘤起源于原发性白血病的共同细胞,尽管偶尔也通过克隆进化产生。将谱系转换与其他疾病,如继发性白血病或慢性白血病的原始细胞期相区分非常重要。虽然直接治疗当前谱系可改善预后,但这些患者的结局仍然较差,生存率低且进展迅速。造血干细胞移植可延长生存期。基于谱系转换风险的管理分层可能有助于检测复发并更及时地提供合适的治疗。正在开发高效且毒性受限的治疗方法以改善极差的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/368e/11927657/dabd4160a90a/bs9-7-e00220-g001.jpg

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