Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
Crit Rev Oncol Hematol. 2012 Jan;81(1):94-102. doi: 10.1016/j.critrevonc.2011.01.014. Epub 2011 Feb 25.
Acute lymphoblastic leukemia (ALL) in adults is an uncommon but devastating malignant proliferation of lymphoid precursors. Treatment programs for adult patients are largely based on pediatric regimens. However, cure rates in adults have been limited to 30-40% for the past several decades as opposed to the 80% cure rate in children. Treatment of adolescents and young adults is evolving with the adoption of more aggressive "pediatric-inspired" treatment programs. The role of allogeneic stem cell transplant is first remission remains controversial in spite of recent data suggesting improved outcomes in patients younger than 35. Kinase inhibitors in combination with standard chemotherapy have significantly improved outcomes in ALL associated with the Philadelphia chromosome. The treatment of ALL in the elderly remains challenging. Promising new agents such as nelarabine and clofarabine may improve the outlook. This article reviews the current state of the art for the treatment of ALL in adults.
成人急性淋巴细胞白血病(ALL)是一种罕见但具有破坏性的淋巴前体细胞恶性增殖。成人患者的治疗方案主要基于儿科方案。然而,在过去几十年中,成人的治愈率一直局限在 30-40%,而儿童的治愈率则为 80%。随着更具侵袭性的“儿科启发”治疗方案的采用,青少年和年轻成人的治疗正在不断发展。尽管最近的数据表明 35 岁以下患者的结局有所改善,但在缓解期进行异基因造血干细胞移植的作用仍存在争议。联合标准化疗的激酶抑制剂显著改善了与费城染色体相关的 ALL 的结局。老年人 ALL 的治疗仍然具有挑战性。有前途的新药物,如奈拉滨和克拉屈滨,可能会改善预后。本文综述了成人 ALL 治疗的最新进展。