Department of Bone Marrow Transplantation, Hebei Yanda Lu Daopei Hospital, Langfang, China.
Leuk Lymphoma. 2022 Dec;63(13):3092-3099. doi: 10.1080/10428194.2022.2118531. Epub 2022 Sep 6.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematopoietic malignancy characterized by poor prognosis even following an allogeneic hematopoietic stem cell transplantation (allo-HSCT). We retrospectively analyzed 15 patients diagnosed with BPDCN who underwent an allo-HSCT with myeloablative conditioning (MAC) at our center. The male to female ratio was 11:4. The median age of 36 (range: 6-70) years, all patients initially presented with extramedullary lesions (13 with cutaneous lesions, 1 in the breast and 1 in the lymph nodes) and involved the bone marrow, two cases were diagnosed as central nervous system leukemia (CNSL). Nine patients were in CR1 and six patients were in CR2 status prior to HSCT. All patients received the MAC regimen and an unmanipulated graft. All patients successfully engraftment and achieved full donor chimerism. One patient developed poor graft function, three patients developed aGVHD (Grade I, II, and IV), and seven patients developed cGVHD (mild in 6; moderate in 1). The median follow-up time for survival was 34 (range: 6-64) months. The primary endpoint, overall leukemia-free survival (LFS) rate and overall survival rate was 73.3 ± 10.5%. Allo-HSCT with MAC is a valid option for BPDCN patients in complete remission.
原始浆细胞样树突细胞肿瘤(BPDCN)是一种罕见的血液恶性肿瘤,即使在进行异基因造血干细胞移植(allo-HSCT)后,预后也很差。我们回顾性分析了在我们中心接受清髓性预处理allo-HSCT 的 15 例 BPDCN 患者。男女比例为 11:4。中位年龄为 36 岁(范围:6-70 岁),所有患者最初均表现为髓外病变(13 例皮肤病变,1 例乳房,1 例淋巴结),并累及骨髓,2 例被诊断为中枢神经系统白血病(CNSL)。HSCT 前,9 例患者处于 CR1,6 例患者处于 CR2 状态。所有患者均接受 MAC 方案和未处理的移植物。所有患者均成功植入并实现完全供者嵌合。1 例患者出现移植物功能不良,3 例患者出现急性移植物抗宿主病(I、II 和 IV 级),7 例患者出现慢性移植物抗宿主病(6 例轻度,1 例中度)。总生存随访时间的中位数为 34 个月(范围:6-64 个月)。主要终点,无白血病总生存率(LFS)和总生存率分别为 73.3±10.5%。MAC allo-HSCT 是完全缓解的 BPDCN 患者的有效选择。