Hehlmann R, Kister P, Willer A, Simon M, Schenk M, Seifarth W, Papakonstantinou G, Saussele S, Kolb H J, Ansari H
III. Medizinische Klinik, Klinikum Mannheim, Universität Heidelberg, Germany.
Leukemia. 1994 Apr;8 Suppl 1:S127-32.
In summary, it can be expected that the availability of unrelated donors will increase the number of CML patients that can be treated curatively with allogeneic BMT. Hydroxyurea has replaced busulfan as first line treatment in CML since it prolongs survival. Ongoing randomized studies comparing IFN-based treatment regimens with standard chemotherapy or IFN-monotherapy probably will answer the question whether IFN can cure a small percentage of CML patients and whether this small percentage can be increased by additional chemotherapy. The present attempts to improve prognostic scores and to apply them to early treatment decisions will allow treatment adaptation more individually. The implications of endogenous retroviral sequences expressed in CML cells are not known now, but may be far reaching.
总之,可以预期,无关供体的可得性将增加能够通过异基因骨髓移植得到根治性治疗的慢性粒细胞白血病患者的数量。由于羟基脲能延长生存期,它已取代白消安成为慢性粒细胞白血病的一线治疗药物。正在进行的将基于干扰素的治疗方案与标准化疗或干扰素单药治疗进行比较的随机研究,可能会回答干扰素是否能治愈一小部分慢性粒细胞白血病患者以及这一小部分患者是否能通过附加化疗而增加的问题。目前改善预后评分并将其应用于早期治疗决策的尝试,将使治疗更具个体化。慢性粒细胞白血病细胞中表达的内源性逆转录病毒序列的影响目前尚不清楚,但可能影响深远。