Crysandt Martina, Brings Kira, Beier Fabian, Thiede Christian, Brümmendorf Tim H, Jost Edgar
a Medical Faculty, Dept. of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation , University Hospital RWTH Aachen , Aachen , Germany.
b Medizinische Klinik und Poliklinik I , Universitätsklinikum Carl Gustav Carus der TU Dresden , Dresden , Germany.
Expert Rev Hematol. 2018 Aug;11(8):625-636. doi: 10.1080/17474086.2018.1494566. Epub 2018 Jul 23.
Germ line predisposition to myeloid neoplasms has been incorporated in the WHO 2016 classification of myeloid neoplasms and acute leukemia. The new category of disease is named hereditary myeloid disorder (HMD). Although most myeloid neoplasms are sporadic, germ line mutations and familial predisposition can contribute to development of chronic myeloid diseases and acute myeloid leukemia. This finding and upcoming frequent use of genome wide detection of molecular aberrations will lead to a higher detection rate of a genetic predisposition and influence treatment decisions. Hereditary predisposition is responsible for 5-10% of myeloid malignancies. Management of affected patients begins by the awareness of treating physicians of the problem and a precise work up of the patient and family members. Areas covered: This review focuses on current knowledge about germ line predisposition for myeloid neoplasms including diagnostic, prognostic, and therapeutic aspects in adult patients. Essential information for clinical routine is provided. Expert commentary: Compared to a patient without predisposition, adaptation of treatment strategy for patients with an HMD is often necessary, especially to avoid higher risk of relapse or higher toxicity during chemotherapy or transplantation. Mistakes in choice of a related donor can be omitted. Relatives at risk of developing a HMD need specific surveillance.
胚系易感性导致的髓系肿瘤已被纳入世界卫生组织2016年髓系肿瘤和急性白血病分类中。这种新的疾病类别被命名为遗传性髓系疾病(HMD)。尽管大多数髓系肿瘤是散发性的,但胚系突变和家族易感性可促使慢性髓系疾病和急性髓系白血病的发生。这一发现以及即将频繁使用的全基因组分子异常检测将导致遗传易感性的检出率更高,并影响治疗决策。遗传性易感性导致5%至10%的髓系恶性肿瘤。对受影响患者的管理始于治疗医生对该问题的认识以及对患者及其家庭成员的精确检查。涵盖领域:本综述重点关注关于髓系肿瘤胚系易感性的当前知识,包括成年患者的诊断、预后和治疗方面。提供了临床常规的基本信息。专家评论:与无易感性的患者相比,HMD患者通常需要调整治疗策略,尤其是为了避免化疗或移植期间更高的复发风险或更高的毒性。可以避免在选择相关供体时出现错误。有患HMD风险的亲属需要进行特定监测。