Mauro Michael J, Talpaz Moshe, Radich Jerald P
Weill Cornell Medical College /New York Presbyterian Hospital, New York, New York.
Clin Adv Hematol Oncol. 2013 Nov;11(11 Suppl 17):1-15.
Chronic myelogenous leukemia (CML) is a slowly progressing malignancy that most often includes a clonal genetic aberration (the Philadelphia chromosome) that results in the BCR-ABL fusion protein, a constitutively activated tyrosine kinase. The management of CML was revolutionized more than a decade ago with the introduction of imatinib, a targeted inhibitor of the BCR-ABL protein. Imatinib has improved outcome and increased survival, but a substantial number of patients will develop resistance or intolerance to therapy. The second-generation tyrosine kinase inhibitors nilotinib and dasatinib are now approved in both the first-line and second-line settings. More recently, ponatinib and bosutinib were approved for resistant or refractory disease. This expansion to the treatment armamentarium has raised questions regarding the best selection and sequencing of agents. Clinical trials are now beginning to address these issues and others. The many treatment options in CML can offer patients improved outcomes, greater quality of life, and increased survival.
慢性粒细胞白血病(CML)是一种进展缓慢的恶性肿瘤,通常包含一种克隆性基因畸变(费城染色体),该畸变会导致BCR-ABL融合蛋白的产生,这是一种持续激活的酪氨酸激酶。十多年前,随着伊马替尼(一种BCR-ABL蛋白的靶向抑制剂)的引入,CML的治疗发生了革命性变化。伊马替尼改善了治疗效果并提高了生存率,但仍有相当数量的患者会对治疗产生耐药性或不耐受。第二代酪氨酸激酶抑制剂尼罗替尼和达沙替尼现已获批用于一线和二线治疗。最近,普纳替尼和博舒替尼获批用于耐药或难治性疾病。治疗手段的这种扩展引发了关于药物最佳选择和用药顺序的问题。目前,临床试验开始着手解决这些问题及其他问题。CML的多种治疗选择可为患者带来更好的治疗效果、更高的生活质量和更长的生存期。