Evidence map›Paper›PMID 40254431›Full record

ArticleInternal medicine (Tokyo, Japan)2025

Successful Treatment of Refractory TAFRO Syndrome with Cyclophosphamide: A Report of Two Cases.

Kaito Nakamura, Kosuke Miki, Satoshi Ota, Tetsuya Hoshi

Abstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kaito NakamuraDepartment of General Internal Medicine, Teine Keijinkai Hospital, Japan.
Kosuke MikiDepartment of General Internal Medicine, Teine Keijinkai Hospital, Japan.
Satoshi OtaDepartment of Pathology, Teine Keijinkai Hospital, Japan.
Tetsuya HoshiDepartment of General Internal Medicine, Teine Keijinkai Hospital, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TAFRO syndrome is a rare, severe, and sometimes refractory condition characterized by thrombocytopenia, anasarca, a fever, reticulin myelofibrosis, and organomegaly. Although several treatment options have been proposed for this condition, there are few reported cases in the literature on successful treatment using cyclophosphamide in patients with TAFRO syndrome. We herein report two cases of refractory TAFRO syndrome successfully treated with intravenous cyclophosphamide. In both cases, after the initial treatment with high-dose glucocorticoids and tocilizumab failed, the administration of intravenous cyclophosphamide led to significant improvement. These cases suggest that intravenous cyclophosphamide may be a viable therapeutic option for refractory TAFRO syndromes.

Indexed as

Castleman DiseaseCyclophosphamideFeverImmunosuppressive AgentsPrimary MyelofibrosisThrombocytopeniaEdemaHumansTreatment OutcomeCyclophosphamideImmunosuppressive AgentsCastleman diseasecyclophosphamideTAFRO syndrome

Identifiers

PMID40254431
PMCPMC12659952

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.