Evidence map›Paper›PMID 35846192›Full record

ArticleEJHaem2022

T-cell lymphoma, B-cell lymphoma, and myelodysplastic syndrome harboring common mutations: Trilineage tumorigenesis from a common founder clone.

Kyoko Yoshihara, Yasuhito Nannya, Ikuo Matsuda, Mami Samori, Nobuto Utsunomiya, Masaya Okada, Seiichi Hirota, Seishi Ogawa, Satoshi Yoshihara

Open access · diamondAbstract readCase Reports
In one paragraph

Article in EJHaem, 2022. 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
0.9field-weighted citation impact, top 25% 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, 11 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

9 authors at 2 institutions in 1 country.

Kyoko YoshiharaDepartment of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
Yasuhito NannyaDepartment of Pathology and Tumor Biology Kyoto University Kyoto Japan.
Ikuo MatsudaDepartment of Surgical Pathology Hyogo College of Medicine Nishinomiya Japan.
Mami SamoriDepartment of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
Nobuto UtsunomiyaDepartment of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
Masaya OkadaDepartment of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
Seiichi HirotaDepartment of Surgical Pathology Hyogo College of Medicine Nishinomiya Japan.
Seishi OgawaDepartment of Pathology and Tumor Biology Kyoto University Kyoto Japan.
Satoshi YoshiharaDepartment of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.ORCID https://orcid.org/0000-0002-8537-2422
Hyogo Medical University · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 64-year-old man with angioimmunoblastic T-cell lymphoma (AITL) subsequently developed diffuse large B-cell lymphoma (DLBCL) and myelodysplastic syndrome (MDS). Genomic profiling of AITL, DLBCL, and MDS samples revealed that the tumor cells from all samples shared common mutations in

Indexed as

angioimmunoblastic T‐cell lymphomacommon mutationsdiffuse large B‐cell lymphomafounder clonemultilineage tumorigenesismyelodysplastic syndrome

Identifiers

PMID35846192
PMCPMC9175790
OpenAlexW4200086289

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.