Pui C H
Department of Hematology/Oncology, St. Jude Children's Hospital, Memphis, TN 38105, USA.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995 Sep-Oct;36(5):322-7.
Current chemotherapy will cure at least 65% of children with acute lymphoblastic leukemia (ALL). The major challenge in ALL is to develop effective risk-directed therapy. This approach seeks to improve outcome, through more intensive therapy, for children at high risk of relapse, while reducing the side effects and long-term complications of treatment for those with a high likelihood of cure. The prognosis remains poor for most children with acute myeloid leukemia (AML). Despite the use of intensive chemotherapy and bone marrow transplantation, only 30% to 40% of these patients are long-term survivors. However, research has identified subgroups of patients who will respond well to therapy that is targeted to their specific biologic subtype of AML. Allogeneic bone marrow transplantation remains the only curative treatment for patients with chronic myeloid leukemia. Current efforts focus on improving risk-directed and subtype-specific treatment for the childhood leukemias. Ultimately, it may be possible to target treatments to the specific genetic lesions of leukemic cells.
目前的化疗至少能治愈65%的急性淋巴细胞白血病(ALL)患儿。ALL面临的主要挑战是开发有效的风险导向疗法。这种方法旨在通过更强化的治疗,改善复发高危儿童的治疗效果,同时减少治愈可能性高的患儿治疗的副作用和长期并发症。大多数急性髓系白血病(AML)患儿的预后仍然很差。尽管使用了强化化疗和骨髓移植,但这些患者中只有30%至40%是长期幸存者。然而,研究已经确定了一些患者亚组,他们对针对其特定AML生物学亚型的疗法反应良好。异基因骨髓移植仍然是慢性髓系白血病患者唯一的治愈性治疗方法。目前的努力集中在改善儿童白血病的风险导向和亚型特异性治疗。最终,有可能针对白血病细胞的特定基因损伤进行治疗。