Division of Hematology and Hematologic Malignancies, University of Utah Huntsman Cancer Institute, Salt Lake City, Utah, USA.
BMC Med. 2011 Aug 26;9:99. doi: 10.1186/1741-7015-9-99.
Although imatinib is firmly established as an effective therapy for newly diagnosed patients with chronic myeloid leukemia (CML), the field continues to advance on several fronts. In this minireview we cover recent results of second generation tyrosine kinase inhibitors in newly diagnosed patients, investigate the state of strategies to discontinue therapy and report on new small molecule inhibitors to tackle resistant disease, focusing on agents that target the T315I mutant of BCR-ABL. As a result of these advances, standard of care in frontline therapy has started to gravitate toward dasatinib and nilotinib, although more observation is needed to fully support this. Stopping therapy altogether remains a matter of clinical trials, and more must be learned about the mechanisms underlying the persistence of leukemic cells with treatment. However, there is good news for patients with the T315I mutation, as effective drugs such as ponatinib are on their way to regulatory approval. Despite these promising data, accelerated or blastic phase disease remains a challenge, possibly due to BCR-ABL-independent resistance.
尽管伊马替尼已被确立为治疗慢性髓性白血病(CML)新诊断患者的有效疗法,但该领域仍在多个方面取得进展。在这篇简评中,我们将介绍新诊断患者使用第二代酪氨酸激酶抑制剂的最新结果,探讨停止治疗的策略现状,并报告用于治疗耐药疾病的新型小分子抑制剂,重点关注针对 BCR-ABL 的 T315I 突变的药物。由于这些进展,一线治疗的标准护理开始倾向于达沙替尼和尼洛替尼,尽管还需要更多的观察来完全支持这一点。完全停止治疗仍然是临床试验的问题,并且需要更多地了解治疗后白血病细胞持续存在的机制。然而,对于携带 T315I 突变的患者来说,有好消息,因为像 ponatinib 这样有效的药物正在获得监管部门的批准。尽管有这些有希望的数据,但加速或成髓细胞样白血病期疾病仍然是一个挑战,可能是由于 BCR-ABL 非依赖性耐药所致。