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我如何治疗费城染色体阴性骨髓增殖性肿瘤的急变期。

How I treat the blast phase of Philadelphia chromosome-negative myeloproliferative neoplasms.

机构信息

Section of Hematology Oncology, Department of Medicine, University of Chicago Comprehensive Cancer Center, The University of Chicago Medicine, Chicago, IL.

出版信息

Blood. 2018 Nov 29;132(22):2339-2350. doi: 10.1182/blood-2018-03-785907. Epub 2018 Oct 17.

Abstract

The classic Philadelphia chromosome (Ph)-negative myeloproliferative neoplasms (MPNs) are a heterogeneous group of hematopoietic stem-cell diseases, characterized by activated JAK/STAT signaling and significant phenotypic mimicry, including a propensity for evolution to myeloid blast phase disease. Effective therapeutic options are limited for patients with Ph MPNs in the blast phase (MPN-BP), and allogeneic stem-cell transplantation is the only known cure. Our increasing understanding of the molecular pathogenesis of this group of diseases, coupled with the increasing availability of targeted agents, has the potential to inform new subset-specific therapeutic approaches. Ultimately, progress in MPN-BP will hinge on prospective clinical and translational investigations with the goal of generating more effective treatment interventions. This case-based review highlights the molecular and clinical heterogeneities of MPN-BP and incorporates a treatment algorithm that underscores the importance of a personalized approach to this challenging group of diseases.

摘要

经典费城染色体(Ph)阴性骨髓增殖性肿瘤(MPN)是一组异质性造血干细胞疾病,其特征为 JAK/STAT 信号的激活和显著的表型模拟,包括向髓系原始细胞危象疾病演变的倾向。Ph MPN 原始细胞危象(MPN-BP)患者的有效治疗选择有限,异基因造血干细胞移植是唯一已知的治愈方法。我们对这群疾病的分子发病机制的认识不断加深,再加上靶向药物的日益普及,有可能为新的亚组特异性治疗方法提供信息。最终,MPN-BP 的进展将取决于以生成更有效治疗干预措施为目标的前瞻性临床和转化研究。本基于病例的综述强调了 MPN-BP 的分子和临床异质性,并纳入了一个治疗算法,强调了对这组具有挑战性疾病采用个性化方法的重要性。

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