Characteristics and prognosis of non-spontaneously regressing immunodeficiency-associated lymphoproliferative disorders in patients with rheumatoid arthritis after methotrexate discontinuation
ObjectiveTo investigate the risk factors and prognosis of non-spontaneously regressing immunodeficiency-associated lymphoproliferative disorders (LPDs) after methotrexate (MTX) discontinuation in patients with rheumatoid arthritis (RA). MethodsWe retrospectively reviewed medical records of 38 patients with MTX-associated LPD and compared the characteristics of those with and without spontaneous regression (SR) of LPDs (SR versus non-SR groups: n = 22 versus 16) and of survivors and non-survivors in the non-SR group (n = 5 deaths). ResultsThe SR and non-SR groups were comparable regarding age, sex, RA duration and activity, MTX use duration and dose, LPD stage and histological characteristics (lymphoma types and Epstein-Barr encoding region in situ hybridisation positivity). However, the non-SR group had significantly higher lactate dehydrogenase (LDH) levels at LPD diagnosis and lower lymphocyte recovery 1 month after MTX withdrawal. Multivariate analysis revealed poor lymphocyte recovery 1 month after MTX withdrawal as a risk factor for non-SR (odds ratio: 7.12; p = 0.02). Log-rank test showed that elevated LDH levels (>250 U/L) were significantly associated with death (p = 0.02). ConclusionsLack of lymphocyte recovery 1 month after MTX discontinuation was a risk factor for non-spontaneously regressive LPD. High LDH level was associated with death in these cases.
Authors
- Hiroshi Kaneko
- Masatoshi Hotta (ORCID: https://orcid.org/0000-0001-6790-8804)
- Hiroyuki Yamashita (ORCID: https://orcid.org/0000-0002-0022-1941)
- M. Wakatsuki (ORCID: https://orcid.org/0009-0004-8639-6911)
Institutions
- National Center for Global Health and Medicine (JP)
Publication Details
- Journal
- Modern Rheumatology
- Published
- 2025-12-09
- DOI
- https://doi.org/10.1093/mr/roaf115
- Primary Topic
- Viral-associated cancers and disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00