Burnett Alan K, Mohite Unmesh
Department of Haematology, University Hospital of Wales, Cardiff, UK.
Semin Hematol. 2006 Apr;43(2):96-106. doi: 10.1053/j.seminhematol.2006.01.003.
The experience of most collaborative study groups is that the outcome for older patients has, unlike in younger patients, failed to improve over the last two decades. In addition there are a substantial number of older patients who do not enter collaborative group trials because they are not considered suitable for an intensive chemotherapy approach. During this era many combinations of chemotherapeutic agents at different dose levels have been tried. It is clear that novel agents and new approaches must be used to improve the situation, and should include options for patients who are not fit for intensive treatment. Fortunately, the increased understanding of the molecular basis and heterogeneity of the disease has fostered the development of novel agents. Chemo-resistance is a key characteristic of acute myeloid leukaemia (AML) in older patients and a number of randomized trials have now been completed to assess this approach. New possibilities of selectively killing leukemic cells and/or modifying toxicity are in prospect with the development of antibody directed chemotherapy in the form of gemtuzumab ozogamicin (Mylotarg; Wyeth, Philadelphia, PA). New drugs such as clofarabine or cloretazine are being evaluated. Molecular mechanisms, whether recognized or not, have been targeted by the use of FLT-3 and farnesyl transferase (FT) inhibitors. With several new agents to evaluate, novel approaches to trial design aimed at detecting options likely to make a useful impact are needed.
大多数协作研究组的经验表明,与年轻患者不同,老年患者的治疗结果在过去二十年中并未得到改善。此外,有相当数量的老年患者未参加协作组试验,因为他们被认为不适合采用强化化疗方法。在这个时期,人们尝试了许多不同剂量水平的化疗药物组合。显然,必须使用新型药物和新方法来改善这种情况,并且应该为不适合强化治疗的患者提供选择。幸运的是,对该疾病分子基础和异质性的深入了解促进了新型药物的开发。化疗耐药是老年急性髓细胞白血病(AML)的一个关键特征,现在已经完成了一些随机试验来评估这种方法。随着以吉妥珠单抗奥唑米星(Mylotarg;惠氏公司,宾夕法尼亚州费城)形式的抗体导向化疗的发展,选择性杀死白血病细胞和/或改变毒性的新可能性正在出现。新型药物如氯法拉滨或氯雷他嗪正在进行评估。分子机制,无论是否被认识到,都已通过使用FLT-3和法尼基转移酶(FT)抑制剂作为靶点。由于有几种新药需要评估,因此需要新的试验设计方法来检测可能产生有益影响的选择。