Lamanna Nicole
Leukemia Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Curr Oncol Rep. 2005 Sep;7(5):333-8. doi: 10.1007/s11912-005-0059-0.
A dramatic change has taken place in therapy for chronic lymphocytic leukemia over the past 15 years. In 1990, available therapy produced complete responses in less than 5% of treated patients. This is in marked contrast to modern regimens, which can reliably produce complete responses in over 50% of patients. This remarkable improvement is completely attributable to the introduction of new active agents. These new agents include three purine analogues (pentostatin, fludarabine, and cladribine) and two monoclonal antibodies (rituximab and alemtuzumab). Novel combinations of these agents have emerged as effective new therapies for previously untreated and pretreated patients. Clinical studies indicate that such combinations can induce higher response rates--including complete responses--than single-agent therapy. Those patients who achieve a complete response have superior survival, compared with those who only achieve a partial response. Though not yet demonstrated in a prospective randomized trial, treatment approaches aimed at achieving high-quality responses may one day lead to an improvement in survival for patients with chronic lymphocytic leukemia and, ultimately, offer the hope of curative therapy in these patients.
在过去15年里,慢性淋巴细胞白血病的治疗发生了巨大变化。1990年,可用的治疗方法在不到5%的接受治疗的患者中产生完全缓解。这与现代治疗方案形成了显著对比,现代治疗方案能在超过50%的患者中可靠地产生完全缓解。这一显著改善完全归因于新的活性药物的引入。这些新药物包括三种嘌呤类似物(喷司他丁、氟达拉滨和克拉屈滨)和两种单克隆抗体(利妥昔单抗和阿仑单抗)。这些药物的新型组合已成为针对既往未治疗和经治疗患者的有效新疗法。临床研究表明,与单药治疗相比,此类组合可诱导更高的缓解率,包括完全缓解率。与仅达到部分缓解的患者相比,实现完全缓解的患者生存期更长。尽管尚未在前瞻性随机试验中得到证实,但旨在实现高质量缓解的治疗方法可能有一天会改善慢性淋巴细胞白血病患者的生存期,并最终为这些患者提供治愈性治疗的希望。