Department of Blood and Marrow Transplantation and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL, USA.
Scholarly Concentrations Program, Biomedical Research, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Br J Haematol. 2018 Mar;180(6):854-862. doi: 10.1111/bjh.15105. Epub 2018 Jan 18.
Hypoalbuminaemia has been previously described to predict worse non-relapse mortality (NRM) and inferior overall survival (OS) in allogeneic haematopoietic cell transplant (allo-HCT) recipients. Here, we evaluate the role of hypoalbuminaemia (<35 g/l) at time of onset of acute graft-versus-host disease (aGVHD) when incorporated into the refined aGVHD score. The study population consisted of 522 patients, median age 53 (18-75) years, who underwent an allo-HCT mostly for haematological malignancies. Standard risk (SR) aGVHD comprised 467 patients (89%) and the number of high risk (HR) cases was 55 (11%). Median follow-up for all surviving patients was 26 (3-55) months. Two-year OS was significantly better in patients with SR aGVHD with a serum albumin ≥35 g/l compared to SR with albumin <35 g/l [70% (95% CI = 64-76%) vs. 49% (95% CI = 42-56%), P < 0·0001]. Also, patients with SR aGVHD and a serum albumin level of ≥35 g/l had a significantly lower NRM at 1-year post-transplantation [6% (95% CI = 3-10%) vs. 25% (95% CI = 20-32%), P < 0·0001]. After our findings are validated in a large cohort of patients, we propose that hypoalbuminaemia should be incorporated into the refined aGVHD risk score to further its ability to predict outcomes within this group.
低蛋白血症先前已被描述为预测异基因造血细胞移植(allo-HCT)受者非复发死亡率(NRM)和总体生存(OS)更差的指标。在这里,我们评估了在急性移植物抗宿主病(aGVHD)发作时低蛋白血症(<35 g/l)的作用,当时它被纳入改良的 aGVHD 评分中。研究人群包括 522 名中位年龄为 53 岁(18-75 岁)的患者,他们主要因血液系统恶性肿瘤接受 allo-HCT。标准风险(SR)aGVHD 包括 467 名患者(89%),高危(HR)病例数为 55 名(11%)。所有存活患者的中位随访时间为 26(3-55)个月。SR aGVHD 患者的血清白蛋白≥35 g/l 组与 SR aGVHD 患者的血清白蛋白<35 g/l 组相比,2 年 OS 显著更好[70%(95% CI=64-76%)比 49%(95% CI=42-56%),P<0·0001]。此外,SR aGVHD 且血清白蛋白水平≥35 g/l 的患者在移植后 1 年时 NRM 显著降低[6%(95% CI=3-10%)比 25%(95% CI=20-32%),P<0·0001]。在大量患者队列中验证我们的发现后,我们建议将低蛋白血症纳入改良的 aGVHD 风险评分中,以进一步提高其预测该组患者结局的能力。