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骨髓增殖性肿瘤患者白血病转化的治疗选择。

Therapeutic options for leukemic transformation in patients with myeloproliferative neoplasms.

作者信息

Khan Maliha, Siddiqi Rabbia, Gangat Naseema

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Department of Internal Medicine, Dow University of Health Sciences, Karachi, Pakistan.

出版信息

Leuk Res. 2017 Dec;63:78-84. doi: 10.1016/j.leukres.2017.10.009. Epub 2017 Oct 27.

Abstract

Approximately 5-10% of patients with Philadelphia chromosome negative myeloproliferative neoplasms (MPN) comprising of essential thrombocythemia, polycythemia vera and primary myelofibrosis) experience transformation to acute myeloid leukemia (AML, ≥20% blasts). Treatment options for post-MPN AML patients are limited, as conventional approaches like standard chemotherapy, fail to offer long-term benefit. Median survival for secondary AML is ∼2.4 months. Post-MPN AML therefore represents an area of urgent clinical need. At present, allogeneic stem cell transplant (ASCT) following induction therapy is the best therapeutic option. Patients ineligible for ASCT are treated with hypomethylating agents. New agents under investigation include histone deacetylase inhibitors, JAKinhibitors and agents targeting the BRD4 protein. Combined treatment strategies involving these novel agents are being tested. In this review we present the current evidence regarding treatment options for post-MPN AML patients.

摘要

约5%-10%的费城染色体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)患者会转化为急性髓系白血病(AML,原始细胞≥20%)。MPN后AML患者的治疗选择有限,因为标准化疗等传统方法无法带来长期益处。继发性AML的中位生存期约为2.4个月。因此,MPN后AML是一个亟待临床解决的领域。目前,诱导治疗后的异基因干细胞移植(ASCT)是最佳治疗选择。不符合ASCT条件的患者采用去甲基化药物治疗。正在研究的新药物包括组蛋白去乙酰化酶抑制剂、JAK抑制剂和靶向BRD4蛋白的药物。涉及这些新型药物的联合治疗策略正在进行测试。在本综述中,我们展示了关于MPN后AML患者治疗选择的当前证据。

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