Teshima Takanori, Matsuo Keitaro, Matsue Kosei, Kawano Fumio, Taniguchi Shuichi, Hara Masamichi, Hatanaka Kazuo, Tanimoto Mitsune, Harada Mine, Nakao Shinji, Abe Yasunobu, Wake Atsushi, Eto Tetsuya, Takemoto Yoshinobu, Imamura Masahiro, Takahashi Satoshi, Ishida Yoji, Kanda Yoshinobu, Kasai Masaharu, Takaue Yoichi
Centre for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka, Japan.
Br J Haematol. 2005 Aug;130(4):575-87. doi: 10.1111/j.1365-2141.2005.05632.x.
The impact of human leucocyte antigen (HLA) incompatibility between donor and recipient on graft-versus-host disease (GVHD) and graft failure after reduced-intensity conditioning stem cell transplantation (RICT) remains to be elucidated. We retrospectively analysed outcome in 341 patients who underwent RICT from related donors for haematological malignancies. The overall cumulative incidence of grade II-IV acute GVHD (aGVHD) was 40% for all subjects; 39% in recipients with HLA-matched donors, 44% in those with one-locus-mismatched donors, and 50% in those with two- to three-loci-mismatched donors. In a Cox regression model adjusted for potential confounders, the tendency for grade II-IV aGVHD (P=0.01), chronic GVHD (cGVHD) (P=0.05) and graft failure (P=0.033) increased with HLA disparity. Use of peripheral blood grafts instead of marrow was a risk factor for cGVHD. Use of antithymocyte globulin was associated with reduced aGVHD and cGVHD. Overall survival (OS) in recipients of two- to three-loci-mismatched RICT at 2 years (18%) was significantly worse than that in patients who received one-locus-mismatched RICT (51%) and HLA-matched RICT (48%) (P<0.0001). A two- to three-loci mismatch was identified as an independent risk factor for OS (P<0.001), but there was no significant difference in OS between HLA-matched and one-locus-mismatched RICT. HLA incompatibility between the donor and recipient is an important risk factor for graft failure, aGVHD, cGVHD and OS after RICT. RICT from a one-locus-mismatched donor may represent an effective alternative approach in patients with high-risk malignancies who lack HLA-matched related donors.
供体与受体之间的人类白细胞抗原(HLA)不相容性对减低强度预处理干细胞移植(RICT)后移植物抗宿主病(GVHD)和移植物失败的影响仍有待阐明。我们回顾性分析了341例因血液系统恶性肿瘤接受来自相关供体的RICT患者的结局。所有受试者II-IV级急性GVHD(aGVHD)的总体累积发生率为40%;HLA匹配供体的受者为39%,一位点错配供体的受者为44%,两位点至三位点错配供体的受者为50%。在针对潜在混杂因素进行调整的Cox回归模型中,II-IV级aGVHD(P=0.01)、慢性GVHD(cGVHD)(P=0.05)和移植物失败(P=0.033)的趋势随着HLA差异增加。使用外周血移植物而非骨髓是cGVHD的一个危险因素。使用抗胸腺细胞球蛋白与aGVHD和cGVHD降低相关。两位点至三位点错配RICT受者的2年总生存率(OS)(18%)显著低于接受一位点错配RICT(51%)和HLA匹配RICT(48%)的患者(P<0.0001)。两位点至三位点错配被确定为OS的独立危险因素(P<0.001),但HLA匹配和一位点错配RICT之间的OS无显著差异。供体与受体之间的HLA不相容性是RICT后移植物失败、aGVHD、cGVHD和OS的重要危险因素。对于缺乏HLA匹配相关供体的高危恶性肿瘤患者,来自一位点错配供体的RICT可能是一种有效的替代方法。