Robert H. Lurie Comprehensive Cancer Center and Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States; Northwestern Medicine Developmental Therapeutics Institute (NMDTI), Northwestern University, Chicago, IL, United States; Jesse Brown Veterans Affairs Medical Center, Chicago, IL, United States.
Robert H. Lurie Comprehensive Cancer Center and Division of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States; Northwestern Medicine Developmental Therapeutics Institute (NMDTI), Northwestern University, Chicago, IL, United States.
EBioMedicine. 2016 Jan 13;3:17-25. doi: 10.1016/j.ebiom.2016.01.010. eCollection 2016 Jan.
Despite the emergence of JAK inhibitors, there is a need for disease-modifying treatments for Philadelphia-negative myeloproliferative neoplasms (MPNs). JAK inhibitors ameliorate symptoms and address splenomegaly, but because of the heterogeneous contributors to the disease process, JAK inhibitor monotherapy incompletely addresses the burden of disease. The ever-growing understanding of MPN pathogenesis has provided the rationale for testing novel and targeted therapeutic agents, as monotherapies or in combination, in preclinical and clinical settings. A number of intriguing options have emerged, and it is hoped that further progress will lead to significant changes in the natural history of MPNs.
尽管 JAK 抑制剂已经出现,但仍需要针对费城阴性骨髓增殖性肿瘤(MPN)的疾病修饰治疗方法。JAK 抑制剂可改善症状并解决脾肿大问题,但由于疾病进程的异质性,JAK 抑制剂单药治疗不能完全解决疾病负担。对 MPN 发病机制的不断深入了解为在临床前和临床环境中测试新型和靶向治疗药物提供了依据,无论是单药治疗还是联合治疗。已经出现了许多有趣的选择,希望进一步的进展将导致 MPN 自然史的重大变化。