Xiao Q Q, Yu X L, Song X C, Hou Y X, Deng L, Li W J, Zhou F
Department of Hematology, The 960th Hospital of The People's Liberation Army (PLA) Joint Logistics Support Force, Jinan 250031, China.
Zhonghua Xue Ye Xue Za Zhi. 2024 Mar 14;45(3):249-256. doi: 10.3760/cma.j.cn121090-20230822-00084.
To analyze the efficacy of allo-HSCT with total body irradiation (TBI) and chemotherapy alone in the treatment of adult ALL and to explore the factors affecting prognosis. The clinical data of 95 adult patients with ALL who underwent allo-HSCT from January 2015 to August 2022 were included. According to the conditioning regimen, the patients were divided into two groups: the TBI plus cyclophosphamide (TBI/Cy) group (=53) and the busulfan plus cyclophosphamide (Bu/Cy) group (=42). Hematopoietic reconstitution after transplantation, GVHD, transplantation-related complications, relapse rate (RR), non-relapse mortality (NRM), OS, and LFS were compared, and the factors related to prognosis were analyzed. The median time of neutrophil engraftment was 14 (10-25) days in the TBI/Cy group and 14 (10-24) days in the Bu/Cy group (=0.106). The median time of megakaryocyte engraftment was 17 (10-42) days in the TBI/Cy group and 19 (11-42) days in the Bu/Cy group (=0.488). The incidence of grade Ⅱ-Ⅳ acute GVHD (aGVHD) in the TBI/Cy and Bu/Cy groups was 41.5% and 35.7%, respectively (=0.565). The incidence of grade Ⅲ-Ⅳ aGVHD in these two groups was 24.5% and 4.8%, respectively (=0.009). The incidence of severe chronic GVHD in the two groups was 16.7% and 13.5%, respectively (=0.689). The incidence of cytomegalovirus infection, Epstein-Barr virus infection, severe infection, and hemorrhagic cystitis in the two groups was 41.5% and 35.7% (=0.565), 34.0% and 35.7% (=0.859), 43.4% and 33.3% (=0.318), and 20.8% and 50.0% (=0.003), respectively. The median follow-up time was 37.1 months and 53.3 months in the TBI/Cy and Bu/Cy groups, respectively. The 2-year cumulative RR was 17.0% in the TBI/Cy group and 42.9% in the Bu/Cy group (=0.017). The 2-year cumulative NRM was 24.5% and 7.1%, respectively (=0.120). The 2-year LFS was 58.5% and 50.0%, respectively (=0.466). The 2-year OS rate was 69.8% and 64.3%, respectively (=0.697). In the multivariate analysis, the conditioning regimen containing TBI was a protective factor for relapse after transplantation (=0.304, 95% 0.135-0.688, =0.004), whereas the effect on NRM was not significant (=1.393, 95% 0.355-5.462, =0.634). Infection was an independent risk factor for OS after allo-HSCT in adult patients with ALL. allo-HSCT based on TBI conditioning regimen had lower relapse rate and lower incidence of hemorrhagic cystitis for adult ALL, compared with chemotherapy regimen. While the incidence o grade Ⅲ/Ⅳ aGVHD was hgher in TBI conditioning regimen than that in chemotherapy regimen.
分析单纯全身照射(TBI)和化疗的异基因造血干细胞移植(allo-HSCT)治疗成人急性淋巴细胞白血病(ALL)的疗效,并探讨影响预后的因素。纳入2015年1月至2022年8月接受allo-HSCT的95例成人ALL患者的临床资料。根据预处理方案,将患者分为两组:TBI加环磷酰胺(TBI/Cy)组(n=53)和白消安加环磷酰胺(Bu/Cy)组(n=42)。比较移植后造血重建、移植物抗宿主病(GVHD)、移植相关并发症、复发率(RR)、非复发死亡率(NRM)、总生存期(OS)和无白血病生存期(LFS),并分析与预后相关的因素。TBI/Cy组中性粒细胞植入的中位时间为14(10-25)天,Bu/Cy组为14(10-24)天(P=0.106)。TBI/Cy组巨核细胞植入的中位时间为17(10-42)天,Bu/Cy组为19(11-42)天(P=0.488)。TBI/Cy组和Bu/Cy组Ⅱ-Ⅳ级急性GVHD(aGVHD)的发生率分别为41.5%和35.7%(P=0.565)。这两组Ⅲ-Ⅳ级aGVHD的发生率分别为24.5%和4.8%(P=0.009)。两组重度慢性GVHD的发生率分别为16.7%和13.5%(P=0.689)。两组巨细胞病毒感染、爱泼斯坦-巴尔病毒感染、严重感染和出血性膀胱炎的发生率分别为41.5%和35.7%(P=0.565)、34.0%和35.7%(P=0.859)、43.4%和33.3%(P=0.318)、20.8%和50.0%(P=0.003)。TBI/Cy组和Bu/Cy组的中位随访时间分别为37.1个月和53.3个月。TBI/Cy组2年累积RR为17.0%,Bu/Cy组为42.9%(P=0.017)。2年累积NRM分别为24.5%和7.1%(P=0.120)。2年LFS分别为58.5%和50.0%(P=0.466)。2年OS率分别为69.8%和64.3%(P=0.697)。多因素分析中,含TBI的预处理方案是移植后复发的保护因素(P=0.304,95%CI 0.135-0.688,P=0.004),而对NRM的影响不显著(P=1.393,95%CI 0.355-5.462,P=0.634)。感染是成人ALL患者allo-HSCT后OS的独立危险因素。与化疗方案相比,基于TBI预处理方案的allo-HSCT治疗成人ALL的复发率较低,出血性膀胱炎的发生率较低。而TBI预处理方案中Ⅲ/Ⅳ级aGVHD的发生率高于化疗方案。