CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Acute Lymphoblastic Leukaemia in the Youngest: Haematopoietic Stem Cell Transplantation and Beyond.
Acute Lymphoblastic Leukaemia in the Youngest: Haematopoietic Stem Cell Transplantation and Beyond.
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ALL SCTped 2012 FORUM(未成年患者免于放疗)试验比较了4岁以下接受急性淋巴细胞白血病(ALL)移植儿童的结局;受试者随机接受以全身照射(TBI)为基础或以化疗为基础的清髓预处理方案。与化疗预处理相比,TBI预处理复发率较低。尽管如此,为避免最脆弱低龄患者发生放射相关并发症,适合接受TBI的年龄界限随时间逐步提高。对于4岁以下儿童,最佳治疗方案仍不明确。出生后第一年确诊ALL的婴儿患者预后显著差于年龄较大儿童。这主要由婴儿ALL的生物学特征所致,婴儿常携带KMT2A基因重排,同时也与其身体脆弱有关。相比之下,1岁以上、4岁以下儿童ALL的临床表现和生物学特征往往更接近较大儿童。本文综述4岁以下儿童造血干细胞移植(HSCT)现状、可用预处理方案,以及可能影响治疗决策的领域新进展。
The ALL SCTped 2012 FORUM (For Omitting Radiation Under Majority age) trial compared outcomes for children 4 years of age transplanted for acute lymphoblastic leukaemia (ALL) who were randomised to myeloablation with a total body irradiation (TBI)-based or chemotherapy-based conditioning regimen. The TBI-based preparation was associated with a lower rate of relapse compared with chemoconditioning. Nevertheless, the age considered suitable for TBI was progressively raised over time to spare the most fragile youngest patients from irradiation-related complications. The best approach to use for children <4 years of age remains unclear.
Children diagnosed with ALL in their first year of life, defined as infants, have a remarkably poorer prognosis compared with older children. This is largely explained by the biology of their ALL, with infants often carrying a KMT2A gene rearrangement, as well as by their fragility.
In contrast, the clinical presentations and biological features of ALL in children >1 year but <4 years often resemble those presented by older children. In this review, we explore the state of the art regarding haematopoietic stem cell transplantation (HSCT) in children <4 years, the preparative regimens available, and new developments in the field that may influence treatment decisions.
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