Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Division of Hematology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Biol Blood Marrow Transplant. 2019 Jul;25(7):1331-1339. doi: 10.1016/j.bbmt.2019.01.033. Epub 2019 Feb 1.
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired clonal hematopoietic cell disease characterized by the destruction of hematopoietic cells through activation of the complement system with manifestations that can be life-threatening including hemolysis, thrombosis, and marrow failure. Allogeneic hematopoietic cell transplantation (HCT) remains the sole cure for PNH, but eculizumab, a terminal complement inhibitor of C5, has been used to prevent complement-mediated hemolysis in patients with PNH since its approval by the Food and Drug Administration in 2007. We examined outcomes of HCT in patients with PNH to evaluate the effects of disease subtype, conditioning intensity, and eculizumab use either pre-HCT or post-HCT. Fifty-five patients with a diagnosis of PNH underwent at least 1 HCT, with 4 patients requiring a second HCT for graft failure. The median age at the time of first HCT was 30.0 years (range, 4.2 to 66.9 years). Seventeen patients (30.9%) had classical PNH, and the remaining 38 patients had PNH associated with another marrow disorder (aplastic anemia in 26 of the 38). Indications for HCT included pancytopenia in 47.3% of the patients, myeloid malignancy (myelodysplastic syndrome, myeloproliferative neoplasm, or acute myelogenous leukemia) in 21.8%, recurrent hemolysis in 20.0%, and thrombosis in 10.9%. Of the 55 first HCTs, 26 were performed with myeloablative conditioning, 27 were performed with reduced-intensity conditioning, and 2 sets of identical twins underwent HCT without any conditioning. Donor types included HLA-matched related in 38.2%, HLA-matched unrelated in 34.5%, single HLA-allele mismatched unrelated in 16.4%, umbilical cord blood in 5.5%, syngeneic in 3.6%, and HLA-haploidentical in 1.8%. The median duration of follow-up in surviving patients was 6.1 years (range, 2.1 to 46.1 years) after first HCT. The median time to neutrophil and platelet engraftment was 17 days and 19 days, respectively; all but 2 patients (96.3%) had sustained engraftment. Overall survival was 70% at 5 years. Neither the choice of conditioning intensity nor PNH subtype affected survival. Nineteen patients died during follow-up, including 12 patients before day +365. Six patients received treatment with eculizumab before HCT, and 2 were treated after HCT. All patients treated with eculizumab were alive at a median follow-up of 2.3 years (range, .2 to 6.9 years). Both patients treated with eculizumab after HCT had minimal to no acute GVHD (aGVHD), with grade I skin aGVHD in 1 patient and no aGVHD in the other patient, and no chronic GVHD at 2.1 and 4.1 years post-HCT, respectively. With the approval of eculizumab, the indications for HCT include persistent hemolysis, persistent thrombosis, and associated marrow failure. Administration of eculizumab before and after HCT warrants further study, particularly considering our observation of minimal to no GVHD in 2 patients who received eculizumab after HCT.
阵发性睡眠性血红蛋白尿症(PNH)是一种罕见的后天性克隆性造血细胞疾病,其特征是通过补体系统的激活导致造血细胞破坏,临床表现可能危及生命,包括溶血、血栓形成和骨髓衰竭。异基因造血细胞移植(HCT)仍然是 PNH 的唯一治愈方法,但 2007 年食品和药物管理局批准使用末端补体抑制剂依库珠单抗预防 PNH 患者的补体介导的溶血以来,它已被用于预防 PNH 患者的补体介导的溶血。我们研究了 PNH 患者 HCT 的结果,以评估疾病亚型、预处理强度以及依库珠单抗在 HCT 前或 HCT 后的使用对结局的影响。55 例 PNH 患者至少接受了 1 次 HCT,其中 4 例因移植物失败需要第 2 次 HCT。首次 HCT 时的中位年龄为 30.0 岁(范围为 4.2 至 66.9 岁)。17 例(30.9%)为经典 PNH,其余 38 例与另一种骨髓疾病相关(38 例中有 26 例为再生障碍性贫血)。HCT 的适应证包括 47.3%的患者全血细胞减少、21.8%的骨髓恶性肿瘤(骨髓增生异常综合征、骨髓增生性肿瘤或急性髓系白血病)、20.0%的复发性溶血和 10.9%的血栓形成。在 55 例首次 HCT 中,26 例采用清髓性预处理,27 例采用强度降低的预处理,2 对同卵双胞胎在无预处理的情况下接受了 HCT。供者类型包括 HLA 匹配的亲缘关系 38.2%、HLA 匹配的无关供者 34.5%、单 HLA 等位基因不匹配的无关供者 16.4%、脐带血 5.5%、同基因 3.6%和 HLA 半相合 1.8%。在首次 HCT 后存活患者的中位随访时间为 6.1 年(范围为 2.1 至 46.1 年)。中性粒细胞和血小板植入的中位时间分别为 17 天和 19 天;除 2 例患者(96.3%)外,所有患者均持续植入。5 年总生存率为 70%。预处理强度的选择和 PNH 亚型均不影响生存。19 例患者在随访期间死亡,其中 12 例在+365 天前死亡。6 例患者在 HCT 前接受了依库珠单抗治疗,2 例患者在 HCT 后接受了治疗。所有接受依库珠单抗治疗的患者在中位随访 2.3 年(范围,0.2 至 6.9 年)时仍存活。在 HCT 后接受依库珠单抗治疗的 2 例患者的急性移植物抗宿主病(GVHD)均较轻至无,其中 1 例患者为 I 级皮肤急性 GVHD,另 1 例患者无急性 GVHD,分别在 HCT 后 2.1 年和 4.1 年无慢性 GVHD。随着依库珠单抗的批准,HCT 的适应证包括持续溶血、持续血栓形成和相关骨髓衰竭。依库珠单抗在 HCT 前和 HCT 后的应用值得进一步研究,特别是考虑到我们观察到在 HCT 后接受依库珠单抗治疗的 2 例患者中,GVHD 较轻至无。