Evidence map›Paper›PMID 36047093›Full record

ArticleInternal medicine (Tokyo, Japan)2022

Combined Therapy with Ixazomib, Lenalidomide, and Dexamethasone for Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes Syndrome.

Tomoki Suichi, Sonoko Misawa, Yukari Sekiguchi, Kazumoto Shibuya, Keigo Nakamura, Hiroki Kano, Yuya Aotsuka, Ryo Otani, Marie Morooka, Shokichi Tsukamoto and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2022. 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
0.5field-weighted citation impact, top 33% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

15 authors at 3 institutions in 1 country.

Tomoki SuichiDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Sonoko MisawaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Yukari SekiguchiDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Kazumoto ShibuyaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Keigo NakamuraDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Hiroki KanoDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Yuya AotsukaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Ryo OtaniDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Marie MorookaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Shokichi TsukamotoDepartment of Hematology, Chiba University Hospital, Japan.
Yusuke TakedaDepartment of Hematology, Chiba University Hospital, Japan.
Naoya MimuraDepartment of Hematology, Chiba University Hospital, Japan.
Chikako OhwadaDepartment of Hematology, Chiba University Hospital, Japan.
Emiko SakaidaDepartment of Hematology, Chiba University Hospital, Japan.
Satoshi KuwabaraDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Chiba University · JPChiba University Hospital · JPInternational University of Health and Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Immunomodulatory drugs and proteasome inhibitors are therapeutic options for polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome. This study aimed to evaluate the efficacy and safety of the combination of ixazomib, lenalidomide, and dexamethasone (IRd) for POEMS syndrome. Methods Six consecutive patients with POEMS syndrome who were treated with the IRd regimen at Chiba University Hospital between April 2018 and August 2021 were included. Serum M-protein and serum vascular endothelial growth factor (sVEGF) levels, overall neuropathy limitation scales (ONLS), clinical symptoms, and adverse events were assessed. Results Of the six patients, five had received prior treatments. Patients received a median of 5 cycles (range, 3-28 cycles) of IRd. Following treatment, serum M-protein disappeared in two patients, sVEGF levels returned to normal in two patients, two patients showed a reduction in the ONLS of 1, and clinical symptoms improved in four patients. The median level of sVEGF decreased from 2,395 pg/mL (range, 802-6,120 pg/mL) to 1,428 pg/mL (range, 183-3,680 pg/mL) in three months. Adverse events, including rash, neutropenia, sensory peripheral neuropathy, and nausea, were observed in three patients, which necessitated dose reduction or discontinuation of treatment. Conclusion IRd can be a therapeutic option for POEMS syndrome, albeit with careful monitoring of adverse events.

Indexed as

Endocrine System DiseasesMonoclonal Gammopathy of Undetermined SignificancePOEMS SyndromeBoron CompoundsDexamethasoneGlycineHumansLenalidomideVascular Endothelial Growth Factor ABoron CompoundsDexamethasoneGlycineixazomibLenalidomideVascular Endothelial Growth Factor Aimmunomodulatory drugsixazomiblenalidomidePOEMS syndromeproteasome inhibitorsvascular endothelial growth factor (VEGF)

Identifiers

PMID36047093
PMCPMC9492490
OpenAlexW4294126064

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.