Department of Hematology, Gunma University, Gunma, Japan.
Division of Hematology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
Bone Marrow Transplant. 2019 Dec;54(12):2020-2026. doi: 10.1038/s41409-019-0585-2. Epub 2019 Jun 11.
Although cytogenetic abnormalities at diagnosis are recognized as an important prognostic factor in patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL), the prognostic impact has not been evaluated in allogeneic stem cell transplant (allo-SCT) recipients. Thus, we assessed 373 Ph-negative ALL patients who underwent allo-SCT. The high-risk (HR) group included those with t(4;11), t(8;14), low hypodiploidy, and complex karyotype, and the standard risk (SR) group included all other karyotypes. Among the 204 patients who underwent a transplant during the first remission (167 in the SR group and 37 in the HR group), the overall survival (OS) rates were similar between these groups (64.1% vs. 80.0% at 5 years, respectively; p = 0.12). Conversely, among the 106 patients who underwent a transplant while not in remission (84 in the SR group and 22 in the HR group), patients in the SR group showed a significantly superior OS rate compared to the HR group (15.4% vs. 4.5% at 5 years, respectively; p = 0.022). These results suggested that treatment outcomes of Ph-negative ALL patients with HR cytogenetic abnormalities may improve following allo-SCT, especially in the first remission. Innovative transplant approaches are warranted in patients who are not in remission.
虽然在诊断时的细胞遗传学异常被认为是费城染色体(Ph)阴性急性淋巴细胞白血病(ALL)患者的一个重要预后因素,但在异基因造血干细胞移植(allo-SCT)受者中尚未评估其预后影响。因此,我们评估了 373 例接受 allo-SCT 的 Ph 阴性 ALL 患者。高危(HR)组包括具有 t(4;11)、t(8;14)、低倍体和复杂核型的患者,标准风险(SR)组包括所有其他核型。在 204 例接受首次缓解期移植的患者中(SR 组 167 例,HR 组 37 例),两组的总生存(OS)率无显著差异(分别为 5 年时的 64.1%和 80.0%;p=0.12)。相反,在 106 例未缓解时接受移植的患者中(SR 组 84 例,HR 组 22 例),SR 组患者的 OS 率明显优于 HR 组(分别为 5 年时的 15.4%和 4.5%;p=0.022)。这些结果表明,HR 细胞遗传学异常的 Ph 阴性 ALL 患者在接受 allo-SCT 后治疗结果可能会改善,尤其是在首次缓解期。对于未缓解的患者,需要有创新的移植方法。