Evidence map›Paper›PMID 40571608›Full record

Observational studyInternal medicine (Tokyo, Japan)2026

Retrospective Study of 68 Patients with Rheumatoid Arthritis-associated Lymphoproliferative Diseases Treated with Methotrexate.

Yuko Asanuma, Yoshiyuki Abe, Ken Yamaji, Naoto Tamura

Abstract readObservational Study
In one paragraph

Observational study in Internal medicine (Tokyo, Japan), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yuko AsanumaDepartment of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Japan.
Yoshiyuki AbeDepartment of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Japan.
Ken YamajiDepartment of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Japan.
Naoto TamuraDepartment of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives This study aimed to investigate the clinical features of lymphoproliferative disease (LPD) in rheumatoid arthritis (RA) patients. Methods We examined the reasons for methotrexate (MTX) discontinuation in 829 patients with RA. In 68 patients with RA whose reason for discontinuation was suspected LPD, blood test results and patient background on the day of MTX discontinuation, pathological characteristics, and the use of biologics after the diagnosis of LPD were analyzed. Results In 829 RA patients in whom MTX was discontinued during the course of treatment, suspected LPD was the fourth most common reason for discontinuation (n=68). Patients who discontinued MTX due to suspected LPD were significantly older and had lower lymphocyte counts, higher serum LDH levels, lower serum albumin levels, higher serum CRP levels, and higher serum soluble interleukin-2 receptor (sIL-2R) levels than patients who discontinued MTX for other reasons. In patients who discontinued MTX due to suspected LPD, the MTX dose used at the time of MTX discontinuation was significantly higher in patients whose lesions regressed spontaneously with MTX discontinuation alone than in patients whose lesions required treatment due to a lack of regression or who died. During the observation period, 16 patients received biologics after LPD regression. LPD did not relapse during the observation period. Conclusions Biologics might be an effective choice for patients with RA after LPD regression, but their safety has not been fully evaluated. Therefore, careful follow-up is required.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidLymphoproliferative DisordersMethotrexateAgedAge FactorsFemaleHumansLymphocyte CountMaleMiddle AgedRetrospective StudiesTreatment OutcomeWithholding TreatmentAntirheumatic AgentsMethotrexatebiologicslymphoproliferative disordersmethotrexaterheumatoid arthritis

Identifiers

PMID40571608
PMCPMC12854946

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.