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染色体核型异常对接受异基因移植的费城染色体阴性成人 ALL 患者预后的影响。

Prognostic impact of cytogenetic abnormalities in adult patients with Philadelphia chromosome-negative ALL who underwent an allogeneic transplant.

机构信息

Department of Hematology, Gunma University, Gunma, Japan.

Division of Hematology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.

出版信息

Bone Marrow Transplant. 2019 Dec;54(12):2020-2026. doi: 10.1038/s41409-019-0585-2. Epub 2019 Jun 11.

Abstract

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.

摘要

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。

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