Evidence map›Paper›PMID 41348001›Full record

ReviewHematology. American Society of Hematology. Education Program2025

Monoclonal-related neuropathies: diagnosis, prognosis, and outcomes.

Arnaud Jaccard, Laurent Magy, Bertrand Arnulf, Frank Bridoux, Murielle Roussel

Registry-linked trialAbstract readReview
In one paragraph

Review in Hematology. American Society of Hematology. Education Program, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07661667 (The Efficacy of Photobiomodulation in the Treatment of Anti-MAG-Induced Peripheral Neuropathy), which is not on this 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.

NCT07661667 enrolling by invitationnot on this mapstarted 2026, after this paper: background citation

The Efficacy of Photobiomodulation in the Treatment of Anti-MAG-Induced Peripheral Neuropathy: LASER-MAG Study.

TypeobservationalSponsorCentre Hospitalier de CornouailleRan2026 to 2026Enrolled10ConditionsAnti MAG NeuropathyArmsphotobiomodulation
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

5 authors.

Arnaud JaccardDepartment of Hematology and Cellular Therapy, National Reference Center for AL Amyloidosis and Other Monoclonal Immunoglobulin Deposit Diseases, University Hospital of Limoges, Limoges, France.
Laurent MagyDepartment and Laboratory of Neurology, Reference Center for Neuromuscular Disorders (AOC), University Hospital of Limoges, Limoges, France.
Bertrand ArnulfDepartment of Hematology and Immunology, National Reference Center for AL Amyloidosis and Other Monoclonal Immunoglobulin Deposit Diseases, Saint-Louis hospital, APHP, Paris Cité University, Paris, France.
Frank BridouxDepartment of Nephrology, National Reference Center for AL Amyloidosis and Other Monoclonal Immunoglobulin Deposit Diseases, University Hospital Poitiers, Poitiers, France.
Murielle RousselDepartment of Hematology and Cellular Therapy, National Reference Center for AL Amyloidosis and Other Monoclonal Immunoglobulin Deposit Diseases, University Hospital of Limoges, Limoges, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal gammopathy is observed in approximately 10% of patients with peripheral neuropathy, which is particularly common in those with the immunoglobulin M monoclonal component. The diagnostic challenge lies in determining whether the neuropathy is causally related to the paraprotein or merely coincidental. Physicians must be familiar with the spectrum of monoclonal gammopathy-associated neuropathies, including anti-myelin-associated glycoprotein neuropathy, amyloid light chain amyloidosis, POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome, CANOMAD (chronic ataxic neuropathy, ophthalmoplegia, IgM paraprotein, cold agglutinins, and disialosyl antibodies), and cryoglobulinemia, as well as their clinical, electrophysiologic, and immunologic characteristics. Initial workup includes serum protein electrophoresis, immunofixation, free light chain analysis, and targeted antibody testing based on the paraprotein and neuropathy phenotype. Close collaboration between neurologists and hematologist-oncologists is essential for accurate diagnosis and appropriate treatment, which may involve both immunotherapy and targeted therapies for the underlying hematologic disorder.

Indexed as

ParaproteinemiasPeripheral Nervous System DiseasesHumansImmunotherapyMolecular Targeted TherapyPrognosis

Identifiers

PMID41348001
PMCPMC12891631

What OpenQuestion holds

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Registered trials

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.