Copelan E A, McGuire E A
Department of Internal Medicine, Ohio State University, Columbus.
Blood. 1995 Mar 1;85(5):1151-68.
Despite reports to the contrary, only a small minority of adults with ALL are currently cured. Results have improved modestly with more intensive postremission chemotherapy and with tailoring of protocols in individuals with specific subsets of ALL. The use of growth factors may further improve treatment results. The performance of allogeneic BMT in first remission is clearly effective in some individuals, eg, those with Ph1-positive ALL, but it is unclear whether it is advantageous in most individuals. There are little data supporting the effectiveness of autotransplantation, as currently performed in ALL, despite its theoretical potential. Advances in understanding the biology of ALL have led to new approaches currently under basic and clinical investigation. These include serial studies of minimal residual disease by a variety of techniques to tailor treatment, the development of conjugated MoAbs to lymphoid cell antigens and immunologic and biochemical approaches to chimeric RNA and peptides generated by abnormal fusion genes. It seems likely that substantial improvement in the treatment of adult ALL awaits better characterization of the biology of this disease. However, some improvement will occur through empirical clinical research. It is critical that physicians recognize the poor results with current therapeutic approaches and enter patients into large well-designed clinical trials.
尽管有相反的报道,但目前只有一小部分成人急性淋巴细胞白血病患者被治愈。随着缓解后化疗强度的增加以及针对特定亚型急性淋巴细胞白血病患者的方案调整,治疗结果有了一定程度的改善。生长因子的使用可能会进一步提高治疗效果。首次缓解期进行异基因骨髓移植对某些患者,如Ph1阳性急性淋巴细胞白血病患者,显然是有效的,但对于大多数患者是否有益尚不清楚。尽管自体移植在理论上有潜力,但目前在急性淋巴细胞白血病治疗中支持其有效性的数据很少。对急性淋巴细胞白血病生物学特性认识的进展催生了目前正在基础和临床研究中的新方法。这些方法包括通过多种技术对微小残留病进行系列研究以调整治疗方案、开发针对淋巴细胞抗原的偶联单克隆抗体以及针对异常融合基因产生的嵌合RNA和肽的免疫和生化方法。成人急性淋巴细胞白血病治疗的显著改善可能有待对该疾病生物学特性有更深入的了解。然而,通过经验性临床研究也会有一些改善。至关重要的是,医生要认识到当前治疗方法效果不佳,并让患者参加大型精心设计的临床试验。