Division of Hematology/Oncology, Department of Internal Medicine, Mayo Clinic, 13400 East Shea Boulevard, Scottsdale, AZ 85259, USA.
Curr Hematol Malig Rep. 2012 Mar;7(1):78-86. doi: 10.1007/s11899-011-0107-9.
The BCR/ABL-negative myeloproliferative neoplasms (MPNs) of essential thrombocythemia, polycythemia vera, and primary myelofibrosis, over the natural course of their disease, have an increasing predisposition to transform to overt acute myeloid leukemia (AML)-most appropriately referred to as MPN-blast phase (MPN-BP). Although this transformation is a rare event, once AML has occurred, it is associated with a poor response to therapy and short survival. The molecular events leading to transformation are poorly defined. Currently, no therapy other than allogeneic stem cell transplantation (ASCT) has been demonstrated to alter the natural history of this disease. Multiple therapeutic investigations are currently ongoing, including early ASCT, hypomethylating agents, and JAK2 inhibition, to try to alter the course of the disease and improve outcomes. This review focuses on the latest advances in our understanding of the biology of leukemic transformation and current clinical therapies that are available for this patient population.
BCR/ABL 阴性骨髓增殖性肿瘤(MPN),包括原发性血小板增多症、真性红细胞增多症和原发性骨髓纤维化,在其自然病程中,存在向显性急性髓系白血病(AML)转化的趋势,最恰当的命名为 MPN-急变期(MPN-BP)。尽管这种转化是一种罕见事件,但一旦发生 AML,其对治疗的反应较差,且生存时间较短。导致转化的分子事件尚不清楚。目前,除了异基因造血干细胞移植(ASCT)之外,尚无其他疗法被证明能够改变这种疾病的自然病程。目前正在进行多项治疗研究,包括早期 ASCT、低甲基化剂和 JAK2 抑制,以试图改变疾病进程并改善预后。本文重点介绍了我们对白血病转化生物学的最新认识,以及目前针对该患者群体的临床治疗方法。