Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawaharacho, Sakyo-ku, Kyoto, 606-8507, Japan.
Division of Cellular Therapy, Duke University Medical Center, Durham, NC, USA.
Int J Hematol. 2011 Apr;93(4):532-541. doi: 10.1007/s12185-011-0820-0. Epub 2011 Apr 5.
To evaluate the clinical significance of subcategory and severity of chronic graft-versus-host disease (GVHD) as defined by the National Institutes of Health (NIH) consensus criteria, we retrospectively studied 211 patients with hematologic neoplasms who survived beyond 100 days after allogeneic hematopoietic cell transplantation. Endpoints included chronic GVHD-specific survival (cGSS), duration of immunosuppressive treatment, and non-relapse mortality (NRM). A total of 96 patients fulfilled the NIH diagnostic criteria for cGVHD. In univariable analysis, patients with NIH overlap syndrome tended to exhibit lower cGSS compared to those with NIH classic cGVHD [hazard ratio (HR) = 2.76, P = 0.060], while patients with severe cGVHD at onset had a significantly lower cGSS compared to those with mild-to-moderate cGVHD (HR = 3.10, P = 0.034). The duration of immunosuppressive treatment was not significantly affected by either subcategory or severity of NIH cGVHD. In multivariable analysis treating cGVHD as a time-dependent covariate, development of overlap syndrome (HR = 3.90, P = 0.014) or severe cGVHD at peak worsening (HR = 6.21, P < 0.001) was significantly associated with higher risk of NRM compared to the absence of cGVHD. Our results suggest that both the subcategory and severity of NIH cGVHD are partly correlated with cGSS and may play a useful role in distinguishing patients at high risk for NRM, warranting validation of this approach through future prospective studies.
为了评估美国国立卫生研究院(NIH)共识标准定义的慢性移植物抗宿主病(cGVHD)亚类和严重程度的临床意义,我们回顾性研究了 211 例异基因造血细胞移植后存活超过 100 天的血液系统恶性肿瘤患者。终点包括 cGVHD 特异性生存(cGSS)、免疫抑制治疗持续时间和非复发死亡率(NRM)。共有 96 例患者符合 NIH 诊断 cGVHD 的标准。单变量分析显示,与 NIH 经典 cGVHD 患者相比,NIH 重叠综合征患者的 cGSS 倾向于降低[风险比(HR)=2.76,P=0.060],而发病时为重度 cGVHD 的患者的 cGSS 明显低于轻度至中度 cGVHD 的患者(HR=3.10,P=0.034)。cGVHD 的亚类或严重程度均不会显著影响免疫抑制治疗的持续时间。在多变量分析中,将 cGVHD 作为时变协变量进行治疗,重叠综合征的发展(HR=3.90,P=0.014)或在疾病进展最严重时出现重度 cGVHD(HR=6.21,P<0.001)与无 cGVHD 患者相比,与 NRM 风险增加显著相关。我们的研究结果表明,NIH cGVHD 的亚类和严重程度与 cGSS 部分相关,可能在区分 NRM 风险高的患者方面发挥有用作用,值得通过未来的前瞻性研究来验证这种方法。