Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hematol Oncol. 2022 Dec;40(5):1041-1055. doi: 10.1002/hon.3046. Epub 2022 Jul 10.
The medium-dose etoposide (VP16) added on cyclophosphamide (CY)/total body irradiation (TBI) is one of the intensified myeloablative conditioning regimens used in allogenic hematopoietic stem cell transplantation (allo-HSCT) for acute lymphoblastic leukemia (ALL). However, the patient subgroups who can actually benefit from VP16/CY/TBI compared to CY/TBI have not been precisely defined. Therefore, we conducted a multi-center retrospective study using the Japanese nationwide registry database to elucidate the efficacy of VP16/CY/TBI on post-transplant prognosis. Biological and clinical distinct subtypes (i.e., Philadelphia chromosome-positive (Ph+) and -negative (Ph-) ALL) were evaluated separately, which included 820 Ph+ and 1463 patients with Ph- ALL, respectively. Compared with the CY/TBI group, the VP16/CY/TBI group showed superior progression-free survival (PFS) in patients with Ph+ ALL (65% vs. 57% at 3 years after HSCT; adjusted hazard ratio (HR), 0.73; 95% confidence interval (CI), 0.55-0.98; p = 0.03), along with significantly reduced incidence of relapse (adjusted HR, 0.58; 95% CI, 0.37-0.90; p = 0.02) without the increase of non-relapse mortality (NRM). By contrast, in patients with Ph- ALL, VP16/CY/TBI did not improve PFS nor incidence of relapse; addition of VP16 reduced relapse (HR, 0.65; p = 0.06) in patients with Ph- ALL transplanted at CR1, while improved PFS was not observed (HR, 0.90; p = 0.52) due to increased NRM. This study demonstrated that VP16/CY/TBI is a more effective and well-tolerated regimen in comparison with CY/TBI in patients with myeloablative allo-HSCT for adult Ph+ ALL. Our findings can provide a novel algorithm for conditioning regimen selection in patients with adult ALL.
中剂量依托泊苷(VP16)联合环磷酰胺(CY)/全身照射(TBI)是异基因造血干细胞移植(allo-HSCT)治疗急性淋巴细胞白血病(ALL)中强化的骨髓清除性预处理方案之一。然而,与 CY/TBI 相比,实际上能从 VP16/CY/TBI 中获益的患者亚组尚未明确界定。因此,我们利用日本全国登记数据库进行了一项多中心回顾性研究,以阐明 VP16/CY/TBI 对移植后预后的疗效。分别评估了生物学和临床上不同的亚型(即费城染色体阳性(Ph+)和阴性(Ph-)ALL),分别包括 820 例 Ph+ALL 和 1463 例 Ph-ALL 患者。与 CY/TBI 组相比,VP16/CY/TBI 组在 Ph+ALL 患者中显示出更好的无进展生存(PFS)(移植后 3 年时分别为 65%和 57%;调整后的风险比(HR)为 0.73;95%置信区间(CI)为 0.55-0.98;p=0.03),且复发率显著降低(调整后的 HR 为 0.58;95%CI 为 0.37-0.90;p=0.02),而非复发死亡率(NRM)没有增加。相比之下,在 Ph-ALL 患者中,VP16/CY/TBI 并未改善 PFS 或复发率;VP16 的添加降低了 CR1 时 Ph-ALL 患者的复发率(HR 为 0.65;p=0.06),但未观察到 PFS 的改善(HR 为 0.90;p=0.52),因为 NRM 增加。这项研究表明,与 CY/TBI 相比,VP16/CY/TBI 是一种更有效且耐受良好的方案,可用于成人 Ph+ALL 的强化 allo-HSCT。我们的研究结果可为成人 ALL 患者的预处理方案选择提供新的方案。