[Retrospective analysis of allogeneic hematopoietic stem cell transplantation for multiple myeloma after myeloablative conditioning with 8 Gy of total body irradiation].

Nobuhiro Tsukada, Moe Yogo, Kodai Kunisada, Yuki Oda, Tomomi Takei, Kota Sato, Mizuki Ogura, Taku Kikuchi, Yu Abe, Kenshi Suzuki, Tadao Ishida
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Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is a curative treatment option for multiple myeloma (MM), but few patients are eligible due to its high risk of treatment-related toxicity and relapse. Here, we report the feasibility and efficacy of allo-SCT after myeloablative conditioning with 8 Gy of total body irradiation (TBI) for reducing relapse of MM. We retrospectively analyzed data from 30 consecutive patients who received allo-SCT for MM after 8 Gy of TBI at Japanese Red Cross Medical Center between 2012 and 2021. Median age at allo-SCT was 47 (range 31-61) years. Stem-cell sources were peripheral blood from an HLA-matched related donor (MRD, n=5), bone marrow from an HLA-matched unrelated donor (MUD, n=5), bone marrow from an HLA-mismatched unrelated donor (MMUD, n=13), and cord blood (n=7). All patients received conditioning with 8 Gy of TBI combined with Flu/Mel (n=28) or others (n=2). Five-year PFS and 5-year OS were 36.7% and 46.2%, respectively. Sixteen patients died during the observation period (12 of primary disease and 4 of treatment-related toxicity). Patients with VGPR or better before allo-SCT had significantly better PFS (p=0.009) and OS (p=0.01) than others. Patients who received MMUD cells tended to have better PFS than those with other cell sources. Our report showed that allo-SCT for MM after 8 Gy of TBI is feasible, and the better PFS of MMUD suggests graft-versus-myeloma effects.

[多发性骨髓瘤异基因造血干细胞移植后髓鞘消融调理与 8 Gy 全身照射的回顾性分析]。
同种异体造血干细胞移植(allo-SCT)是多发性骨髓瘤(MM)的一种根治性治疗方法,但由于其治疗相关毒性和复发风险较高,符合条件的患者很少。在此,我们报告了在进行8 Gy全身照射(TBI)的髓脱落调理后进行异体干细胞移植以减少MM复发的可行性和疗效。我们回顾性分析了 2012 年至 2021 年期间在日本红十字医疗中心接受 8 Gy 全身照射后异体 SCT 治疗 MM 的 30 例连续患者的数据。接受异体干细胞移植时的中位年龄为 47 岁(31-61 岁)。干细胞来源包括 HLA 匹配的亲缘供者外周血(MRD,5 人)、HLA 匹配的非亲缘供者骨髓(MUD,5 人)、HLA 不匹配的非亲缘供者骨髓(MMUD,13 人)和脐带血(7 人)。所有患者都接受了 8 Gy TBI 结合 Flu/Mel (28 人)或其他疗法(2 人)的治疗。5年PFS和5年OS分别为36.7%和46.2%。16名患者在观察期内死亡(12名死于原发性疾病,4名死于治疗相关毒性)。同种异体移植前VGPR或更好的患者的PFS(p=0.009)和OS(p=0.01)明显优于其他患者。接受MMUD细胞的患者的PFS往往优于接受其他细胞来源的患者。我们的报告显示,8 Gy TBI后异体SCT治疗MM是可行的,MMUD较好的PFS提示了移植物抗骨髓瘤效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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