Department of Hematology and Oncology, Tokai University School of Medicine, Kanagawa, Japan.
Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Cytotherapy. 2022 Sep;24(9):954-961. doi: 10.1016/j.jcyt.2022.03.004. Epub 2022 May 7.
An intensified conditioning regimen incorporating medium-dose etoposide (VP16) is an option for patients with acute lymphoblastic leukemia (ALL). However, the prognostic impacts of the addition of VP16 to cyclophosphamide (CY) and total body irradiation (TBI) in patients with Philadelphia chromosome-positive (Ph+) ALL with regard to minimal residual disease (MRD) status have not been elucidated.
The authors retrospectively compared the outcomes of patients with Ph+ ALL who underwent allogeneic transplantation following VP16/CY/TBI (n = 101) and CY/TBI (n = 563).
At 4 years, the VP16/CY/TBI group exhibited significantly better disease-free survival (DFS) (72.6% versus 61.7%, P = 0.027) and relapse rate (11.5% versus 21.1%, P = 0.020) and similar non-relapse mortality (16.0% versus 17.2%, P = 0.70). In subgroup analyses, the beneficial effects of the addition of VP16 on DFS were more evident in patients with positive MRD status (71.2% versus 48.4% at 4 years, P = 0.022) than those with negative MRD status (72.8% versus 66.7% at 4 years, P = 0.24). Although MRD positivity was significantly associated with worse DFS in patients who received CY/TBI (48.4% versus 66.7%, P < 0.001), this was not the case in those who received VP16/CY/TBI (71.2% versus 72.8%, P = 0.86).
This study demonstrated the benefits of the addition of VP16 in Ph+ ALL patients, especially those with positive MRD status. VP16/CY/TBI could be a potential strategy to overcome the survival risk of MRD positivity.
对于费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)患者,含中剂量依托泊苷(VP16)的强化预处理方案是一种选择。然而,VP16 联合环磷酰胺(CY)和全身照射(TBI)在 Ph+ALL 患者中的应用对微小残留病(MRD)状态的预后影响尚未阐明。
作者回顾性比较了接受 VP16/CY/TBI(n=101)和 CY/TBI(n=563)异基因移植的 Ph+ALL 患者的结局。
4 年时,VP16/CY/TBI 组无病生存率(DFS)(72.6%对 61.7%,P=0.027)和复发率(11.5%对 21.1%,P=0.020)显著更好,非复发死亡率相似(16.0%对 17.2%,P=0.70)。亚组分析显示,VP16 对 DFS 的有益作用在 MRD 阳性患者中更为明显(4 年时为 71.2%对 48.4%,P=0.022),而在 MRD 阴性患者中则不明显(4 年时为 72.8%对 66.7%,P=0.24)。虽然在接受 CY/TBI 的患者中,MRD 阳性与 DFS 较差显著相关(48.4%对 66.7%,P<0.001),但在接受 VP16/CY/TBI 的患者中则不然(71.2%对 72.8%,P=0.86)。
本研究表明,VP16 的加入对 Ph+ALL 患者有益,尤其是 MRD 阳性患者。VP16/CY/TBI 可能是克服 MRD 阳性生存风险的一种潜在策略。