Evidence map›Paper›PMID 33148934›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2020

Clinicopathological evaluation of methotrexate-associated lymphoproliferative disorders with special focus on Epstein-Barr virus-positive mucocutaneous lesions.

Sawako Shiraiwa, Yara Yukie Kikuti, Joaquim Carreras, Ryujiro Hara, Yasuyuki Aoyama, Daisuke Ogiya, Rikio Suzuki, Masako Toyosaki, Ken Ohmachi, Yoshiaki Ogawa and 4 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  5. Analysis of Notch1 protein expression in methotrexate-associated lymphoproliferative disorders.Journal of clinical and experimental hematopathology : JCEH · 2024
    Article
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  7. Review
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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

14 authors at 2 institutions in 1 country.

Sawako ShiraiwaDepartment of Pathology, Tokai University, School of Medicine, Isehara, Japan.
Yara Yukie KikutiDepartment of Pathology, Tokai University, School of Medicine, Isehara, Japan.
Joaquim CarrerasDepartment of Pathology, Tokai University, School of Medicine, Isehara, Japan.
Ryujiro HaraDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Yasuyuki AoyamaDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Daisuke OgiyaDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Rikio SuzukiDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Masako ToyosakiDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Ken OhmachiDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Yoshiaki OgawaDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Hiroshi KawadaDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Shinji SatoDepartment of Rheumatology, Tokai University School of Medicine, Isehara, Japan.
Naoya NakamuraDepartment of Pathology, Tokai University, School of Medicine, Isehara, Japan.
Kiyoshi AndoDepartment of Hematology and Oncology, Tokai University, School of Medicine, Isehara, Japan.
Tokai University · JPTokai University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some patients diagnosed with methotrexate-associated lymphoproliferative disorder (MTX-LPD) develop spontaneous regression upon the discontinuation of MTX, whereas others require chemotherapy. The mechanisms underlying this differential response and the capacity to spontaneously regress are not clearly understood. We evaluated numerous clinicopathological features in 63 patients diagnosed with MTX-LPD, with a special focus on those with Epstein-Barr virus (EBV)-positive mucocutaneous lesions (EBVMCL). The diagnosis of EBVMCL included cases of both EBV-positive mucocutaneous ulcers (EBVMCU) and diffuse gingival swelling associated with proliferation of EBV-positive large B-cells. Of the four subgroups of MTX-LPD, one-year treatment-free survival (TFS) after the discontinuation of MTX was achieved among those with EBVMCL (100%), diffuse large B-cell lymphoma (57%), Hodgkin-like lesions (60%), or classical Hodgkin lymphoma (29%); a significant difference in TFS was observed when comparing the responses of patients with EBVMCL to the those diagnosed with other subtypes. Multivariate analysis revealed predictive factors for prolonged TFS that included EBV-positive lesions and comparatively low levels of serum LDH. Taken together, our study suggests that a diagnosis of EBVMCL is related to the overall clinical outcome after the discontinuation of MTX.

Indexed as

Epstein-Barr Virus InfectionsHodgkin DiseaseLymphoma, Large B-Cell, DiffuseAdultAgedAged, 80 and overDisease-Free SurvivalFemaleHerpesvirus 4, HumanHumansMaleMethotrexateMiddle AgedRetrospective StudiesSurvival RateMethotrexateEpstein-Barr virusLymphomaMethotrexate-associated lymphoproliferative disorderMucocutaneous ulcerPrognosis

Identifiers

PMID33148934
PMCPMC7810250
OpenAlexW3097575200

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.