Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, New York.
Division of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Clin Adv Hematol Oncol. 2022 Jul;20(7):456-467.
Myelofibrosis (MF) is a myeloproliferative neoplasm driven by constitutive activation of the JAK/STAT pathway, resulting in clonal hematopoiesis, fibrotic replacement of the bone marrow, extramedullary hematopoiesis, splenomegaly, and debilitating constitutional symptoms. The advent of JAK inhibitors has changed the landscape of treatment options for patients with MF, providing relatively tolerable drug options that control symptoms, reduce splenomegaly, and improve quality of life, but often at the expense of worsening cytopenias. JAK inhibitors do not appear to halt the progression of disease or prevent leukemic transformation, and their effect on survival is debated. Here, we review both the US Food and Drug Administration-approved JAK inhibitors and those in late-phase clinical trials, with a focus on clinical activity and unique adverse effects. We also provide a schema for choosing among these options for patients with MF.
骨髓纤维化(MF)是一种由 JAK/STAT 通路组成性激活驱动的骨髓增殖性肿瘤,导致克隆性造血、骨髓纤维化替代、骨髓外造血、脾肿大和衰弱的全身症状。JAK 抑制剂的出现改变了 MF 患者的治疗选择格局,提供了相对耐受的药物选择,可控制症状、减少脾肿大并改善生活质量,但往往以恶化细胞减少为代价。JAK 抑制剂似乎并不能阻止疾病的进展或预防白血病转化,其对生存的影响存在争议。在这里,我们回顾了美国食品和药物管理局批准的 JAK 抑制剂和处于后期临床试验阶段的 JAK 抑制剂,重点关注临床活性和独特的不良反应。我们还为 MF 患者在这些选择之间提供了一个方案。