Evidence map›Paper›PMID 41330907›Full record

ArticleBlood cancer journal2025

Lymphoma risk in autoimmune diseases with multiple medication use: analysis from the LIFE Study.

Ami Inokuchi, Haryoon Kim, Masatoshi Sakurai, Kyoko Masuda, Kota Mizuno, Yuya Koda, Eri Matsuki, Yasunori Kogure, Shoko Ukita, Megumi Maeda and 5 more

Abstract read
In one paragraph

Article in Blood cancer journal, 2025. 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

15 authors.

Ami InokuchiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-1079-6888
Haryoon KimDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Masatoshi SakuraiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Kyoko MasudaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Kota MizunoDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yuya KodaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Eri MatsukiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yasunori KogureDivision of Molecular Oncology, National Cancer Center Research Institute, Tokyo, Japan.ORCID 0000-0003-1158-5131
Shoko UkitaBiostatistics Unit, Clinical and Translational Research Center, Keio University Hospital, Tokyo, Japan.ORCID 0009-0007-3042-329X
Megumi MaedaDepartment of Health Care Administration and Management, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Futoshi OdaDepartment of Health Care Administration and Management, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Yuko KanekoDivision of Rheumatology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yasunori SatoDepartment of Biostatistics, Keio University School of Medicine, Tokyo, Japan.
Haruhisa FukudaDepartment of Health Care Administration and Management, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan. fukuda.haruhisa.977@m.kyushu-u.ac.jp.
Keisuke KataokaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan. kkataoka-tky@umin.ac.jp.ORCID 0000-0002-8263-9902

Funding

MEXT | Japan Science and Technology Agency (JST) JPMJFR205JMEXT | Japan Society for the Promotion of Science (JSPS) JP20H00563MEXT | Japan Society for the Promotion of Science (JSPS) JP21H05051
6 · The paper itself

Abstract

Autoimmune diseases (AIDs) are associated with an increased risk of lymphoma. Although treatment strategies have changed substantially in AIDs, recent evidence regarding this association is lacking. Particularly, the impact of novel immunosuppressive/immunomodulatory agents and the cumulative effect of multiple medication use on lymphoma risk have not been well investigated. To address these, we used the LIFE Study database, which contains health care claims data from 2014 to 2023 in 15 municipalities in Japan. Of 2,229,423 individuals, 211,592 had AIDs and 530 subsequently developed lymphoma. Overall, AID cases had a significantly higher incidence of lymphoma than non-AID cases (hazard ratio [HR] 1.9). Among 23 AIDs, lymphoma risk was significantly elevated in 14, including Takayasu arteritis (6.6) and adult-onset Still's disease (4.7). Among immunosuppressive/immunomodulatory agents, calcineurin inhibitors, iguratimod, or methotrexate were associated with higher lymphoma risks. Importantly, the use of two or more medications strongly increased lymphoma risk (HR 2.7) in AID cases. Lymphoma subtype-specific analysis revealed novel associations, including T/NK-cell lymphoma in systemic lupus erythematosus. Our large-scale cohort study reveals an increased risk of lymphoma in AID patients, particularly those receiving multiple immunosuppressants/immunomodulators, underscoring the need for careful monitoring in these patients.

Indexed as

Autoimmune DiseasesImmunosuppressive AgentsLymphomaAdolescentAdultAgedAged, 80 and overFemaleHumansIncidenceJapanMaleMiddle AgedRisk FactorsYoung AdultImmunosuppressive Agents

Identifiers

PMID41330907
PMCPMC12789534

What OpenQuestion holds

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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.