Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran; Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Biol Blood Marrow Transplant. 2017 Dec;23(12):2110-2117. doi: 10.1016/j.bbmt.2017.08.036. Epub 2017 Sep 1.
Hematopoietic stem cell transplantation (HSCT) with a non-total body irradiation (TBI) conditioning regimen has proven feasible for treating patients with acute lymphoblastic leukemia (ALL). However, it is commonly believed that for extramedullary involvement of ALL in sanctuary sites, such as the central nervous system (CNS), TBI shall not be abandoned. In this study, the outcomes of pediatric ALL patients with CNS involvement (CNS) and without CNS involvement (CNS) treated with TBI-free allogeneic HSCT were retrospectively compared. The patients received a TBI-free busulfan plus cyclophosphamide conditioning regimen. Comparing CNS (n = 27) and CNS (n = 134) patients, the 5-year probabilities of relapse (44.4% versus 41.8%; P = .799), disease-free survival (DFS; 48.1% versus 43.3%; P = .642) and overall survival (OS; 51.9% versus 47.0%; P = .646) were not significantly different. Although transplantation-related mortality (TRM) was higher in the CNS patients, the difference between the 2 groups was not significant (3.7% versus 12.7%; P = .177). In multivariate analysis, there were no significant between-group differences in OS (P = .502), DFS (P = .424), relapse rate (P = .226), or TRM (P = .117). These findings suggest that HSCT using a non-TBI-containing conditioning regimen can lead to similar outcomes in pediatric ALL patients with and without CNS involvement. TBI-free allogeneic HSCT might be feasible and effective for CNS ALL patients.
非全身照射(TBI)预处理的造血干细胞移植(HSCT)已被证明可用于治疗急性淋巴细胞白血病(ALL)患者。然而,人们普遍认为,对于 ALL 在外周避难所部位(如中枢神经系统(CNS))的髓外侵犯,不应放弃 TBI。在这项研究中,回顾性比较了接受无 TBI 异基因 HSCT 治疗的伴有和不伴有中枢神经系统(CNS)受累的儿童 ALL 患者的结局。患者接受了无 TBI 的白消安加环磷酰胺预处理方案。比较 CNS(n=27)和 CNS(n=134)患者,5 年复发率(44.4%与 41.8%;P=0.799)、无病生存率(DFS;48.1%与 43.3%;P=0.642)和总生存率(OS;51.9%与 47.0%;P=0.646)无显著差异。尽管 CNS 患者的移植相关死亡率(TRM)较高,但两组之间的差异无统计学意义(3.7%与 12.7%;P=0.177)。多变量分析显示,OS(P=0.502)、DFS(P=0.424)、复发率(P=0.226)和 TRM(P=0.117)之间无显著组间差异。这些发现表明,采用无 TBI 预处理方案的 HSCT 可使伴有和不伴有 CNS 受累的儿童 ALL 患者获得相似的结局。无 TBI 异基因 HSCT 可能对 CNS ALL 患者可行且有效。