Ma Xiao, Wu De-pei, Sun Ai-ning, Fu Zheng-zheng, Tang Xiao-wen, Wu Xiao-jin, Liu Yue-jun, Qiu Hui-ying, Miao Miao, Han Yue, Jin Zheng-ming, Zhao Ye, Xue Sheng-li, Wang Ying, Chen Su-ning, He Guang-sheng, Zhou Hai-xia, Chang Hui-rong
Department of Hematology, Jiangsu Institute of Hematology, First Affiliated Hospital of Soochow University, Key Laboratory of Thrombosis and Haemostasis, Ministry of Health, Suzhou 215006, China.
Zhonghua Xue Ye Xue Za Zhi. 2009 Feb;30(2):73-6.
To explore the efficacy and toxicity of allogeneic hematopoietic stem cell transplantation (allo-HSCT) for relapsed/refractory acute lymphocytic leukemia (ALL).
Forty-seven patients with relapsed/refractory ALL received allo-HSCT, which containing 19/47 from HLA-identical sibling donors (sib-HSCT), 18/47 from HLA-identical unrelated donors (URD-HSCT) and 10/47 from haplo-identical donors (Hi-HSCT). Conditioning regimens included "TBI plus Cyclophosphamide (Cy) (42/ 47)" or "busulfan (Bu) plus Cy (5/47)". Cyclosporine (CsA) combined with a short-course Methotrexate (MTX) were used for graft versus host disease (GVHD) prophylaxis. In addition, patients receiving URD-HSCT or Hi-HSCT were given mycophenolate mofetil (MMF) and anti-thymocyte immunoglobulin (ATG). Patients with molecular or cytogenetic relapse tendency on minimal residual disease (MRD) monitoring received donor lymphocyte infusion (DLI).
All patients tolerated the therapy well except for mucositis. Renal dysfunction occurred in 2 patients on CsA therapy. Epilepsy occurred in 1 patient, fatal infectious complications in 9 (including 3 interstitial pneumonia), grade III-IV acute GVHD (aGVHD) in 7, chronic GVHD (cGVHD) in 22 and hemorrhagic cystitis (HC) in 4 patients. Thirteen patients relapsed after transplantation. The median time of hematopoietic reconstitution was + 17 ds. Nineteen patients received DLI, and 6 of them had no disease progression. With a median follow-up duration of 43 (10-77) months, the estimated 5-year overall survival (OS) and disease free survival (DFS) rates were 49.65% and 46.55%, respectively.
Allo-HSCT is an effective therapy for relapsed/refractory ALL. Relapse after transplantation, fatal infection, and severe acute GVHD are the main causes for failure. DLI might decrease the relapse rate after transplantation.
探讨异基因造血干细胞移植(allo-HSCT)治疗复发/难治性急性淋巴细胞白血病(ALL)的疗效及毒性。
47例复发/难治性ALL患者接受allo-HSCT,其中19例/47例来自人类白细胞抗原(HLA)全相合的同胞供者(同胞HSCT),18例/47例来自HLA全相合的非血缘供者(URD-HSCT),10例/47例来自单倍体相合供者(Hi-HSCT)。预处理方案包括“全身照射(TBI)加环磷酰胺(Cy)(42例/47例)”或“白消安(Bu)加Cy(5例/47例)”。采用环孢素(CsA)联合短疗程甲氨蝶呤(MTX)预防移植物抗宿主病(GVHD)。此外,接受URD-HSCT或Hi-HSCT的患者给予霉酚酸酯(MMF)和抗胸腺细胞免疫球蛋白(ATG)。微小残留病(MRD)监测显示有分子或细胞遗传学复发倾向的患者接受供者淋巴细胞输注(DLI)。
除黏膜炎外,所有患者对治疗耐受性良好。2例接受CsA治疗的患者出现肾功能不全。1例患者发生癫痫发作,9例出现致命性感染并发症(包括3例间质性肺炎),7例发生Ⅲ-Ⅳ级急性移植物抗宿主病(aGVHD),22例发生慢性移植物抗宿主病(cGVHD),4例患者出现出血性膀胱炎(HC)。13例患者移植后复发。造血重建的中位时间为+17天。19例患者接受了DLI,其中6例无疾病进展。中位随访时间为(10 - 77)个月,估计5年总生存率(OS)和无病生存率(DFS)分别为49.65%和46.55%。
allo-HSCT是治疗复发/难治性ALL的有效方法。移植后复发、致命性感染和严重急性GVHD是治疗失败的主要原因。DLI可能降低移植后复发率。