Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Biol Blood Marrow Transplant. 2019 Jan;25(1):e23-e27. doi: 10.1016/j.bbmt.2018.08.006. Epub 2018 Aug 10.
Acute panmyelosis with myelofibrosis (APMF) is a rare subtype of acute myeloid leukemia characterized by acute onset of cytopenias and bone marrow fibrosis in the absence of splenomegaly. Because the prognosis of APMF is extremely poor even after chemotherapy, hematopoietic cell transplantation (HCT) has been used to treat APMF. However, the outcome after HCT for APMF remains unclear. To evaluate the outcomes and prognostic factors after HCT as a therapeutic modality for APMF, we retrospectively analyzed the Japanese registration data of 40 APMF patients who received allogeneic and syngeneic HCT between 2005 and 2015. The median age at HCT was 53.5 years (range, 16 to 70). The disease status at HCT was first complete remission (CR1) in 13 patients (33%). The probability of overall survival and the cumulative incidence of relapse at 3 years were 24% and 59%, respectively. Univariate analysis identified that female sex and disease status CR1 at the time of HCT were significantly associated with higher overall survival. Although APMF patients have a poor long-term prognosis even after syngeneic and allogeneic HCT, these data suggested that allogeneic HCT offered a curative option for APMF.
急性全髓细胞增多伴骨髓纤维化(APMF)是一种罕见的急性髓系白血病亚型,其特征为无脾肿大的血细胞减少症和骨髓纤维化急性发作。由于即使在化疗后 APMF 的预后也非常差,因此已将造血细胞移植(HCT)用于治疗 APMF。然而,APMF 患者接受 HCT 后的结局仍不清楚。为了评估作为 APMF 治疗方法的 HCT 后的结局和预后因素,我们回顾性分析了 2005 年至 2015 年间接受同种异体和同基因 HCT 的 40 名 APMF 患者的日本注册数据。HCT 时的中位年龄为 53.5 岁(范围,16 至 70 岁)。HCT 时的疾病状态为首次完全缓解(CR1)的有 13 例(33%)。3 年时的总生存率和累积复发率分别为 24%和 59%。单因素分析表明,女性和 HCT 时的疾病状态 CR1 与总生存率显著相关。尽管 APMF 患者即使在接受同基因和同种异体 HCT 后也具有不良的长期预后,但这些数据表明同种异体 HCT 为 APMF 提供了一种治愈选择。