Zhu Guang-hua, Qin Mao-quan, Wang Bin, Zhou Xuan, Yang Jun, Jia Chen-guang, Wu Ying, Wang Xi-si, Wu Min-yuan
The Hematology and Oncology Center, Beijing Children's Hospital, Beijing 100045, China.
Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):807-12.
Osteopetrosis is a rare genetic disorder and the malignant infantile osteopetrosis (MIOP) is the worst subtype of this disease. Seventy percent of patients die in six years of life without proper treatment. Hematopoietic stem cell transplantation (HSCT) offers the only chance of cure for MIOP.
Retrospective analysis was performed on 8 patients with MIOP who underwent HSCT in Beijing Children's Hospital during the period from 2006 to 2011.
Eight cases (4 male and 4 female, mean age at HSCT 13.5 months) were diagnosed as malignant infantile osteopetrosis. Conditioning regimen included fludarabine, busulfan and cyclophosphamide. All patients received cyclosporin for prophylaxis of graft vs. host disease (GvHD). A UMD recipient underwent CD34(+) cell selection. ATG/ALG, mycophenolate mofetil (MMF) and methotrexate (MTX) used for recipients with unrelated cord donor (2) and recipients with haplo-identical donors (5). Average time for neutrophil engraftment was 15.7 day (9 - 36), platelet engraftment was 43.3 day (10 - 68). The patients were followed up from 47 days to 5 years, 1 patient died of post-transplant complications. Seven cases presented better in clinical manifestation. Acute GvHD I°-II° was observed in 6 patients, III°-IV° in 2 patients. It was controlled by anti-GvHD therapy.
Non-allogenic stem cell transplantation treatment of infantile MIOP showed high survival rate and restoration of hematopoiesis in haploid transplant patients, therefore, non-allogenic HSCT may be an option to treat MIOP in children.
骨质石化症是一种罕见的遗传性疾病,恶性婴儿型骨质石化症(MIOP)是该疾病最严重的亚型。70%的患者在6岁前若未得到恰当治疗便会死亡。造血干细胞移植(HSCT)是治愈MIOP的唯一机会。
对2006年至2011年期间在北京儿童医院接受HSCT的8例MIOP患者进行回顾性分析。
8例(4男4女,HSCT时平均年龄13.5个月)被诊断为恶性婴儿型骨质石化症。预处理方案包括氟达拉滨、白消安和环磷酰胺。所有患者均接受环孢素预防移植物抗宿主病(GvHD)。1例脐血移植受者接受了CD34(+)细胞选择。2例无关脐血供者受者和5例单倍体相合供者受者使用了抗胸腺细胞球蛋白/抗淋巴细胞球蛋白(ATG/ALG)、霉酚酸酯(MMF)和甲氨蝶呤(MTX)。中性粒细胞植入的平均时间为15.7天(9 - 36天),血小板植入时间为43.3天(10 - 68天)。对患者进行了47天至5年的随访,1例患者死于移植后并发症。7例患者临床表现改善。6例患者出现I° - II°急性GvHD,2例患者出现III° - IV°急性GvHD。通过抗GvHD治疗得到控制。
非亲缘性干细胞移植治疗婴儿型MIOP显示出较高的生存率,且单倍体移植患者造血功能得以恢复,因此,非亲缘性HSCT可能是治疗儿童MIOP的一种选择。