Ikegame Kazuhiro, Kaida Katsuji, Fukunaga Keiko, Osugi Yuko, Yoshihara Kyoko, Yoshihara Satoshi, Ishii Shinichi, Fujino Satoshi, Yamashita Takaya, Mayumi Azusa, Maruyama Satoshi, Teramoto Masahiro, Inoue Takayuki, Okada Masaya, Tamaki Hiroya, Ogawa Hiroyasu, Fujimori Yosihiro
Division of Hematology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Division of Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Bone Marrow Transplant. 2021 Jan;56(1):70-83. doi: 10.1038/s41409-020-0980-8. Epub 2020 Jun 20.
HLA haploidentical hematopoietic stem cell transplantation (HSCT), i.e., HSCT from a 1-HLA-haplotype-mismatched family donor, has been successfully performed even as a second transplantation for posttransplant relapse. Is the haploidentical the limit of HLA mismatches in HSCT? In order to explore the possibility of HLA-mismatched HSCT from family donors beyond haploidentical relatives, we conducted a prospective phase I/II study of 2-HLA-haplotype-mismatched HSCT (2-haplo-mismatch HSCT). We enrolled 30 patients with posttransplant relapse (acute myeloid leukemia: 18, acute lymphoblastic leukemia: 11, non-Hodgkin lymphoma: 1). 2-haplo-mismatch HSCT was performed as the second to sixth transplantations. The donors were siblings (n = 12), cousins (n = 16), and second cousins (n = 2). The conditioning regimen consisted of fludarabine, cytarabine, melphalan, low-dose anti-thymocyte globulin, and 3 Gy of total body irradiation. Graft-versus-host disease (GVHD) prophylaxis consisted of tacrolimus, methylprednisolone, and mycophenolate mofetil. All patients achieved neutrophil engraftment, except for a case of early death. The cumulative incidences of grades II-IV and III-IV acute GVHD were 36.7% and 16.7%, respectively. The overall survival at 1 year, relapse, and non-relapse mortality rates was 30.1%, 38.9%, and 44.3%, respectively. Considering the poor prognosis of posttransplant relapse, 2-haplo-mismatch HSCT can be an alternative option in a second or third transplantation.
人类白细胞抗原(HLA)单倍型相合造血干细胞移植(HSCT),即来自1个HLA单倍型不相合的家族供者的HSCT,即使作为移植后复发的二次移植也已成功实施。单倍型相合是HSCT中HLA不相合的极限吗?为了探索来自单倍型相合亲属以外的家族供者进行HLA不相合HSCT的可能性,我们开展了一项关于2个HLA单倍型不相合HSCT(2-单倍型不相合HSCT)的前瞻性I/II期研究。我们纳入了30例移植后复发的患者(急性髓系白血病:18例,急性淋巴细胞白血病:11例,非霍奇金淋巴瘤:1例)。2-单倍型不相合HSCT作为第二次至第六次移植进行。供者为兄弟姐妹(n = 12)、堂/表亲(n = 16)和第二代堂/表亲(n = 2)。预处理方案包括氟达拉滨、阿糖胞苷、美法仑、低剂量抗胸腺细胞球蛋白和3 Gy全身照射。移植物抗宿主病(GVHD)预防方案包括他克莫司、甲泼尼龙和霉酚酸酯。除1例早期死亡病例外,所有患者均实现中性粒细胞植入。II-IV级和III-IV级急性GVHD的累积发生率分别为36.7%和16.7%。1年总生存率、复发率和非复发死亡率分别为30.1%、38.9%和44.3%。考虑到移植后复发的预后较差,2-单倍型不相合HSCT可作为第二次或第三次移植的一种替代选择。