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急性髓细胞白血病:关注新的治疗策略。

Acute myeloid leukemia: focus on novel therapeutic strategies.

机构信息

Division of Hematology/Oncology, Department of Internal Medicine, University of Kansas, Kansas City, KS.

出版信息

Clin Med Insights Oncol. 2012;6:205-17. doi: 10.4137/CMO.S7244. Epub 2012 May 16.

Abstract

Acute myeloid leukemia (AML) is a heterogeneous disease with variable clinical outcomes. Cytogenetic analysis reveals which patients may have favorable risk disease, but 5-year survival in this category is only approximately 60%, with intermediate and poor risk groups faring far worse. Advances in our understanding of the biology of leukemia pathogenesis and prognosis have not been matched with clinical improvements. Unsatisfactory outcomes persist for the majority of patients with AML, particularly the elderly. Novel agents and treatment approaches are needed in the induction, post-remission and relapsed settings. The additions of clofarabine for relapsed or refractory disease and the hypomethylating agents represent recent advances. Clinical trials of FLT3 inhibitors have yielded disappointing results to date, with ongoing collaborations attempting to identify the optimal role for these agents. Potential leukemia stem cell targeted therapies and treatments in the setting of minimal residual disease are also under investigation. In this review, we will discuss recent advances in AML treatment and novel therapeutic strategies.

摘要

急性髓系白血病(AML)是一种具有不同临床表现的异质性疾病。细胞遗传学分析揭示了哪些患者可能患有预后良好的疾病,但这一类别患者的 5 年生存率仅约为 60%,而中危和高危组的预后则差得多。我们对白血病发病机制和预后生物学的认识进展并没有转化为临床改善。大多数 AML 患者的结局仍不理想,尤其是老年人。在诱导缓解、缓解后和复发情况下需要新的药物和治疗方法。在复发或难治性疾病中添加氯法拉滨和低甲基化剂是最近的进展。FLT3 抑制剂的临床试验迄今为止结果令人失望,目前正在进行合作,试图确定这些药物的最佳作用。针对微小残留病的潜在白血病干细胞靶向治疗和治疗方法也在研究中。在这篇综述中,我们将讨论 AML 治疗的最新进展和新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1f3/3362331/979a8db79464/cmo-6-2012-205f1.jpg

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