| Literature DB >> 33585232 |
Xiaolei Wei1, Jingxia Zheng1, Zewen Zhang2, Qiongzhi Liu3, Minglang Zhan1, Weimin Huang1, Junjie Chen1, Qi Wei1, Yongqiang Wei1, Ru Feng1.
Abstract
The prognostic value of albumin changes between diagnosis and end-of-treatment (EoT) in diffuse large B-cell lymphoma (DLBCL) remains unknown. We retrospectively analyzed 574 de novo DLBCL patients treated with R-CHOP from our and two other centers. All patients were divided into a training cohort (n = 278) and validation cohort (n = 296) depending on the source of the patients. Overall survival (OS) and progression-free survival (PFS) were analyzed by the method of Kaplan-Meier and Cox proportional hazard regression model. In the training cohort, 163 (58.6%) patients had low serum albumin at diagnosis, and 80 of them were present with consecutive hypoalbuminemia at EoT. Patients with consecutive hypoalbuminemia showed inferior OS and PFS (p = 0.010 and p = 0.079, respectively). Similar survival differences were also observed in the independent validation cohort (p = 0.006 and p = 0.030, respectively). Multivariable analysis revealed that consecutive hypoalbuminemia was an independent prognostic factor OS [relative risk (RR), 2.249; 95% confidence interval (CI), 1.441-3.509, p < 0.001] and PFS (RR, 2.001; 95% CI, 1.443-2.773, p < 0.001) in all DLBCL patients independent of IPI. In conclusion, consecutive hypoalbuminemia is a simple and effective adverse prognostic factor in patients with DLBCL, which reminds us to pay more attention to patients with low serum albumin at EoT during follow-up.Entities:
Keywords: albumin; change; diffuse large B-cell lymphoma; outcome; survival
Year: 2021 PMID: 33585232 PMCID: PMC7873605 DOI: 10.3389/fonc.2020.610681
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244