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原发性巨球蛋白血症患者进行干细胞移植的结果:日本血液和骨髓移植学会(JSHCT)淋巴瘤工作组的分析。

Outcome of stem cell transplantation for Waldenström's macroglobulinemia: analysis of the Japan Society for Hematopoietic Cell Transplantation (JSHCT) Lymphoma Working Group.

机构信息

Division of Hematology, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

Department of Hematology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.

出版信息

Ann Hematol. 2020 Jul;99(7):1635-1642. doi: 10.1007/s00277-020-04078-3. Epub 2020 May 18.

Abstract

The role of stem cell transplantation (SCT) for patients with Waldenström's macroglobulinemia (WM) remains undetermined. Therefore, we retrospectively evaluated the outcome of autologous and allogeneic SCT for patients with WM using the registry database of the Japan Society for Hematopoietic Cell Transplantation. Forty-six patients receiving autologous and 31 receiving allogeneic SCT were analyzed. The allogeneic SCT group included more patients with advanced disease status at transplant and received more lines of chemotherapy. The cumulative incidences of non-relapse mortality (NRM) at 1 year were 30.0% (95% CI, 14.7-46.9%) in the allogeneic SCT and 0% in the autologous SCT group. The estimated 3-year overall (OS) and progression-free (PFS) survival rates were 84.5% (95% CI, 66.0-93.4%) and 70.8% (95% CI, 53.0-82.9%) in the autologous SCT group, and 52.2% (95% CI, 32.5-68.6%) and 45.0% (95% CI, 26.3-62.0%) in the allogeneic SCT group. No patients died after the first 2 years following allogeneic SCT. In univariate analyses, disease status at SCT was significantly associated with PFS in autologous SCT, and with OS and PFS in allogeneic SCT. These results suggest that both autologous and allogeneic SCT have each potential role in WM. Allogeneic SCT is more curative for WM, but is associated with high NRM.

摘要

自体和异体造血干细胞移植治疗华氏巨球蛋白血症的疗效比较

日本造血细胞移植学会注册数据库研究

自体和异体造血干细胞移植(SCT)治疗华氏巨球蛋白血症(WM)的作用仍未确定。因此,我们使用日本造血细胞移植学会的注册数据库,回顾性分析了 WM 患者接受自体和异体 SCT 的结果。分析了 46 例接受自体和 31 例接受异体 SCT 的患者。异体 SCT 组在移植时疾病状态更晚期,接受了更多线的化疗。异体 SCT 组 1 年非复发死亡率(NRM)的累积发生率为 30.0%(95%CI,14.7-46.9%),而自体 SCT 组为 0%。自体 SCT 组的估计 3 年总生存(OS)和无进展生存(PFS)率分别为 84.5%(95%CI,66.0-93.4%)和 70.8%(95%CI,53.0-82.9%),异体 SCT 组分别为 52.2%(95%CI,32.5-68.6%)和 45.0%(95%CI,26.3-62.0%)。异体 SCT 后 2 年内无患者死亡。单因素分析显示,SCT 时的疾病状态与自体 SCT 的 PFS 显著相关,与异体 SCT 的 OS 和 PFS 显著相关。这些结果表明,自体和异体 SCT 在 WM 中都有各自的作用。异体 SCT 对 WM 更具疗效,但与高 NRM 相关。

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