Savage D G, Goldman J M
LRF Centre for Adult Leukaemia, Royal Postgraduate Medical School, London, UK.
Int J Hematol. 1994 Jul;60(1):1-21.
In the past two decades there have been a number of advances in the treatment of chronic myeloid leukemia (CML) in chronic phase. There has been very little progress in the management of advanced disease. Hydroxyurea and interferon-alpha have replaced busulfan as first-line therapy in chronic phase. Hydroxyurea provides excellent control of the disease for periods of months or years and has little toxicity. Interferon-alpha induces a reduction in the Philadelphia chromosome in a substantial minority of patients. Interferon-alpha may also prolong survival. Neither hydroxyurea nor interferon-alpha is able to cure the disease. Patients in chronic phase may be cured by allogeneic bone marrow transplantation (BMT). This procedure has a number of limitations, however, including limited availability, high cost, and substantial morbidity and mortality. Current challenges in BMT are to increase its applicability, to reduce graft-versus-host disease, and to augment graft-versus-leukemia effects. The role of autologous transplantation in CML remains speculative.
在过去二十年中,慢性期慢性髓性白血病(CML)的治疗取得了诸多进展。而晚期疾病的管理进展甚微。羟基脲和α干扰素已取代白消安成为慢性期的一线治疗药物。羟基脲能在数月或数年时间内很好地控制病情,且毒性很小。α干扰素能使相当一部分少数患者的费城染色体减少。α干扰素也可能延长生存期。羟基脲和α干扰素都无法治愈该疾病。慢性期患者可通过异基因骨髓移植(BMT)治愈。然而,该手术存在诸多限制,包括可及性有限、成本高昂以及较高的发病率和死亡率。目前骨髓移植面临的挑战是扩大其适用性、减少移植物抗宿主病并增强移植物抗白血病效应。自体移植在慢性髓性白血病中的作用仍存在推测性。