Levitt L, Lin R
Department of Medicine, Stanford University School of Medicine, California, USA.
West J Med. 1996 Feb;164(2):143-55.
The molecular analysis of acute lymphoblastic leukemia (ALL) has provided exciting insights into the pathogenesis of this disease. This disease is heterogenous and can be subtyped based on chromosomal, immunophenotypic, and structural criteria. The varying prognostic implications of different ALL subtypes markedly influence the treatment decisions in adults. Many patients with T-cell ALL can be cured with chemotherapy alone. In contrast, patients with early B-lineage ALL with certain chromosomal abnormalities, especially the Philadelphia chromosome, do not have durable responses to chemotherapy and should receive a bone marrow transplantation if an HLA-matched donor is available. Recent reports have shown improved results for adults with B-cell ALL (Burkitt's) after intensive alternating cycles of chemotherapy containing high doses of methotrexate and cyclophosphamide. Future clinical and laboratory investigation should lead to the development of novel and possibly more effective treatments specifically tailored for different subsets of ALL.
急性淋巴细胞白血病(ALL)的分子分析为该疾病的发病机制提供了令人兴奋的见解。这种疾病具有异质性,可根据染色体、免疫表型和结构标准进行亚型分类。不同ALL亚型的不同预后意义显著影响成人的治疗决策。许多T细胞ALL患者仅通过化疗即可治愈。相比之下,具有某些染色体异常,尤其是费城染色体的早期B系ALL患者,对化疗没有持久反应,如果有HLA匹配的供体,应接受骨髓移植。最近的报告显示,接受含高剂量甲氨蝶呤和环磷酰胺的强化交替化疗周期后,成人B细胞ALL(伯基特氏)患者的治疗效果有所改善。未来的临床和实验室研究应能开发出专门针对ALL不同亚群的新型且可能更有效的治疗方法。