Lounder Dana T, Khandelwal Pooja, Chandra Sharat, Jordan Michael B, Kumar Ashish R, Grimley Michael S, Davies Stella M, Bleesing Jack J, Marsh Rebecca A
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Biol Blood Marrow Transplant. 2017 May;23(5):857-860. doi: 10.1016/j.bbmt.2017.02.011. Epub 2017 Feb 17.
Hemophagocytic lymphohistiocytosis (HLH) is an immune regulatory disorder that commonly presents with central nervous system (CNS) involvement. The only cure for genetic HLH is hematopoietic stem cell transplantation (HSCT), typically treated with reduced-intensity conditioning (RIC) regimens. We sought to estimate the incidence of CNS relapse after RIC HSCT, determine risk factors, and evaluate outcomes. We performed a retrospective chart review of 94 consecutive children and young adults with primary HLH who received RIC HSCT. CNS relapse within 1 year after transplantation was diagnosed by review of clinical symptoms, cerebral spinal fluid (CSF), and radiologic findings. Four (4.25%) patients developed symptoms of possible CNS HLH after HSCT and 3 patients were diagnosed. Eight patients underwent screening lumbar puncture because of history of active CNS disease at the onset of the conditioning regimen and 4 had evidence of continued disease. The overall incidence of CNS relapse and continued CNS disease after RIC HSCT was 8%. All patients with CNS disease after HSCT responded to CNS-directed therapy. Whole blood donor chimerism at the time of CNS relapse was low at 1% to 34%, but it remained high at 88% to 100% for patients with continued CNS disease. Overall survival for patients with CNS relapse was 50%, compared with 75% for patients without CNS disease (P = .079). Our data suggest that a low level of donor chimerism or active CNS disease at the time of transplantation increase the risk of CNS HLH after HSCT. Surveillance CSF evaluation after allogeneic RIC HSCT should be considered in patients with risk factors and CNS-directed treatment should be initiated if appropriate.
噬血细胞性淋巴组织细胞增生症(HLH)是一种免疫调节紊乱疾病,常伴有中枢神经系统(CNS)受累。遗传性HLH的唯一治愈方法是造血干细胞移植(HSCT),通常采用减低强度预处理(RIC)方案进行治疗。我们试图估算RIC HSCT后CNS复发的发生率,确定危险因素,并评估预后。我们对94例接受RIC HSCT的原发性HLH儿童和青年进行了回顾性病历审查。通过审查临床症状、脑脊液(CSF)和影像学检查结果来诊断移植后1年内的CNS复发。4例(4.25%)患者在HSCT后出现可能的CNS HLH症状,3例被确诊。8例患者因在预处理方案开始时存在活动性CNS疾病史而接受了腰椎穿刺筛查,其中4例有疾病持续存在的证据。RIC HSCT后CNS复发和CNS疾病持续存在的总发生率为8%。所有HSCT后出现CNS疾病的患者对针对CNS的治疗均有反应。CNS复发时全血供体嵌合率较低,为1%至34%,但CNS疾病持续存在的患者该嵌合率仍较高,为88%至100%。CNS复发患者的总生存率为50%,无CNS疾病患者为75%(P = 0.079)。我们的数据表明,移植时供体嵌合率低或存在活动性CNS疾病会增加HSCT后CNS HLH的风险。对于有危险因素的患者,应考虑在异基因RIC HSCT后进行CSF监测评估,如有必要应启动针对CNS的治疗。