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成人费城染色体阳性急性淋巴细胞白血病患者从中剂量 VP16 联合 CY/TBI 的预处理方案中获益。

Adult patients with Ph+ ALL benefit from conditioning regimen of medium-dose VP16 plus CY/TBI.

机构信息

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.

出版信息

Hematol Oncol. 2022 Dec;40(5):1041-1055. doi: 10.1002/hon.3046. Epub 2022 Jul 10.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95c2/10084153/54ed926a2f6a/HON-40-1041-g004.jpg

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