| Literature DB >> 33651193 |
Xin Cao1,2,3,4, Yi-Lin Kong1,2,3, Li Wang1,2,3, Jin-Hua Liang1,2,3, Yi Xia1,2,3, Hua-Yuan Zhu1,2,3, Lei Fan1,2,3, Sheng-Hua Jiang4, Hong Liu4, Jian-Yong Li1,2,3, Wei Xu5,6,7.
Abstract
Waldenstrom macroglobulinemia (WM) is a rare type of non-Hodgkin lymphoma with great heterogeneity, and the data of peripheral blood T-lymphocyte subsets in WM are limited. This study aimed to investigate the clinical correlation and distribution of circulating T-lymphocyte subsets in newly diagnosed WM patients. We retrospectively searched medical records for 86 newly diagnosed WM patients. Comparisons of the absolute CD3+ T-lymphocyte count (ACD3C), CD4+ T-lymphocyte count (ACD4C), CD8+ T-lymphocyte count (ACD8C), and CD4+/CD8+ T-lymphocyte ratio (CD4+/CD8+) as continuous parameters in different groups were calculated. Univariate and multivariate analyses were used to assess prognostic factors for overall survival (OS) and progression-free survival (PFS). Young patients (<65 years) had lower ACD8C levels and a higher CD4+/CD8+ ratio. And the lower level of β2-microglobulin (<3 mg/L) was associated with a higher CD4+/CD8+ ratio. With a median follow-up of 25 months, the univariate survival analysis showed that CD4+/CD8+ ratio inversion (CD4+/CD8+<1.5) was associated with shorter OS and PFS, and multivariate analysis confirmed that inverted CD4+/CD8+ ratio could be an independent adverse prognostic factor for OS and PFS. Additionally, initial treatment with rituximab or bortezomib significantly improved the PFS and OS of CD4+/CD8+ inversion patients but did not affect normal CD4+/CD8+ patients. We show that low circulating CD4+/CD8+ ratio at diagnosis is an adverse prognostic factor in WM patients and that first-line therapy which included rituximab or bortezomib significantly improved PFS and OS for patients with CD4+/CD8+ ratio less than 1.5.Entities:
Keywords: Prognosis; T-lymphocyte subsets; Waldenstrom macroglobulinemia
Year: 2021 PMID: 33651193 DOI: 10.1007/s00277-021-04474-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673