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The clinical impact of absolute lymphocyte count in peripheral blood among patients with methotrexate - associated lymphoproliferative disorders.

Authors :
Tokuhira M
Tanaka Y
Takahashi Y
Kimura Y
Tomikawa T
Anan T
Watanabe J
Sagawa M
Higashi M
Momose S
Amano K
Tabayashi T
Nakaseko R
Tamaru JI
Kizaki M
Source :
Journal of clinical and experimental hematopathology : JCEH [J Clin Exp Hematop] 2020 Jun 20; Vol. 60 (2), pp. 41-50. Date of Electronic Publication: 2020 May 13.
Publication Year :
2020

Abstract

Regressive lymphoproliferative disorders (R-LPD) after methotrexate (MTX) withdrawal are one of the specific features of methotrexate - associated lymphoproliferative disorders (MTX-LPD). Although the impact of the absolute lymphocyte count (ALC) on the pathogenesis of R-LPD has been recently emphasized, understanding relapse/regrowth events (RRE) and differences among LPD subtypes is necessary. In this study, we confirmed ALC recovery in the regressive group (R-G; R-LPD without RRE) and relapse/regrowth group (R/R-G; R-LPD with RRE). The increase in ALC lasted at least 2 years in R-G, whereas it decreased within 3 years in R/R-G, supporting the better overall survival (OS) in R-G, as previously reported. In addition, our study suggested that an ALC of 1000/µL at the time of development of LPD is a significant predictor for treatment-free survival (TFS). Furthermore, an ALC of 1000/µL at 6 months after MTX withdrawal was found to be a significant indicator of TFS and OS for R-G and R/R-G. The ALC decreased gradually before LPD development in R/R-G, whereas it decreased 6 months before LPD development in R-G, confirming the important role of ALC in the pathogenesis of MTX-LPD such as regressive events and RRE. In addition to ALC, other predictive factors, such as serum C-reactive protein and soluble interleukin-2 receptors, may be helpful in the management of MTX-LPD, including the decision making for an additional chemotherapy for regressive LPD after MTX withdrawal.

Details

Language :
English
ISSN :
1880-9952
Volume :
60
Issue :
2
Database :
MEDLINE
Journal :
Journal of clinical and experimental hematopathology : JCEH
Publication Type :
Academic Journal
Accession number :
32404570
Full Text :
https://doi.org/10.3960/jslrt.19039