Evidence map›Paper›PMID 37365854›Full record

ArticleCancer science2023

Lymphoproliferative disorder risk after methotrexate treatment for rheumatoid arthritis.

Keisuke Tanaka, Ayako Ichikawa, Natsuka Umezawa, Kouhei Yamamoto, Kota Yoshifuji, Keigo Okada, Ayako Nogami, Yoshihiro Umezawa, Toshikage Nagao, Chizuko Sakashita and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.9field-weighted citation impact, top 5% of its field
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

14 citing papers in PubMed, 17 citations in OpenAlex.

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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

15 authors at 1 institution in 1 country.

Keisuke TanakaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Ayako IchikawaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Natsuka UmezawaDepartment of Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan.
Kouhei YamamotoDepartment of Pathology, Tokyo Medical and Dental University, Tokyo, Japan.
Kota YoshifujiDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Keigo OkadaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Ayako NogamiDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Yoshihiro UmezawaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Toshikage NagaoDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Chizuko SakashitaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Takehiko MoriDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Shuji TohdaDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.
Ryuji KoikeDepartment of Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan.
Shinsuke YasudaDepartment of Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan.
Masahide YamamotoDepartment of Hematology, Tokyo Medical and Dental University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3142-8806
Tokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methotrexate (MTX)-associated lymphoproliferative disorder (MTX-LPD) is a troublesome problem in patients receiving MTX for rheumatoid arthritis (RA). However, its incidence, prognosis, and risk factors remain unclear. In this retrospective study, we evaluated the actual incidence, prognostic impact, and risk factors of MTX-LPD. Of the 986 patients with RA treated with MTX, 90 patients experienced 95 new malignancies (NMs), with LPD as the most frequent in 26 patients. The cumulative LPD incidences were 1.3% and 4.7% at 5 and 10 years after MTX initiation, respectively. Among the 24 patients who discontinued MTX after developing LPD, 15 showed sustained regression, without difference in overall survival between patients with LPD and without NM. Inflammatory markers and absolute lymphocyte counts were not useful for early LPD development detection, but most of the patients with LPD had persistently elevated erythrocyte sedimentation ratios. Regarding concomitant drugs, tacrolimus increased the risk only if patients were not receiving biological disease-modifying antirheumatic drugs (bDMARDs). bDMARDs did not increase the risk for any of the drugs or the number of classes used. The number of LPD cases was lower in patients with IL-6A even after a long period after MTX, although with no statistically significant difference. Thus, approximately 1 in 20 patients with RA developed MTX-LPD over the 10 years of MTX treatment, but it did not affect the survival of patients with RA. Tacrolimus increased the risk of developing LPD for certain patients and should be used with caution.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidLymphoproliferative DisordersHumansMethotrexateRetrospective StudiesTacrolimusAntirheumatic AgentsMethotrexateTacrolimuscumulative incidenceMTX-LPDrheumatoid arthritisrisk factors

Identifiers

PMID37365854
PMCPMC10475769
OpenAlexW4382182631

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.