Evidence map›Paper›PMID 39196376›Full record

ReviewAnnals of hematology2025

Light chain deposition disease: pathogenesis, clinical characteristics and treatment strategies.

Raffaella Cassano Cassano, Angelo Giovanni Bonadio, Maria Livia Del Giudice, Domenico Giannese, Sara Galimberti, Gabriele Buda

Abstract readReview
In one paragraph

Review in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Pulmonary plasma cell disorders: histopathology, diagnosis, and clinical perspectives.Virchows Archiv : an international journal of pathology · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. 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

6 authors.

Raffaella Cassano CassanoDepartment of Clinical and Experimental Medicine, Hematology, University of Pisa, 56126, Pisa, Italy. cassano462@gmail.com.ORCID http://orcid.org/0009-0008-3156-3857
Angelo Giovanni BonadioDepartment of Surgical, Medical, Molecular Pathology and Critical Area, Division of Surgical Pathology II, University of Pisa, Via Paradisa 2, 56124, Pisa, Italy.
Maria Livia Del GiudiceDepartment of Clinical and Experimental Medicine, Hematology, University of Pisa, 56126, Pisa, Italy.
Domenico GianneseDepartment of Clinical and Experimental Medicine, Nephrology Unit, University of Pisa, 56126, Pisa, Italy.
Sara GalimbertiDepartment of Clinical and Experimental Medicine, Hematology, University of Pisa, 56126, Pisa, Italy.
Gabriele BudaDepartment of Clinical and Experimental Medicine, Hematology, University of Pisa, 56126, Pisa, Italy. gabriele.buda@unipi.it.ORCID http://orcid.org/0000-0002-5240-5611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Light chain deposition disease (LCDD) is a rare hematologic disorder characterized by the deposition of non-amyloid monoclonal light chains in several organs. Together with renal impairment is being the primary morbidity associated with this disease. Due to its rarity, randomized clinical trials lack to explore treatment strategies and there are no approved or universally accepted standard of care treatment options. We aimed to provide a systematic summary of histological and clinical aspects of LCDD and treatment options of available literature therapies strategies. Currently, drugs used to treat multiple myeloma are recommended when LCDD patients also presented multiple myeloma. Anyway, in patients with LCDD that is not associated to multiple myeloma, haematopoietic stem cell transplantation (ASCT) and chemotherapy with thalidomide, dexamethasone, bortezomib are also recommended. In eligible patients, bortezomib-based chemotherapy followed by ASCT appears to be an effective treatment option with durable hematologic remission and organ responses. Although it appears that the patients undergoing ASCT seem to achieve deeper and durable hematologic remissions and organ responses, no statistically significant superiority can be demonstrated over non-transplant or standard chemotherapy-based approaches. As retrieved by our review, bortezomib-based therapy appears to be favorable strategy as long as no dose modification is required for renal impairment, and early hematologic responses as a recovery of renal function. Encouraging data were also demonstrated by treatment lenalidomide or melpalan based. Moreover, new myeloma treatment strategies, as monoclonal antibody Daratumumab, seem to be effective in LCDD. Instead, renal allograft is not recommended, due to high incidence of relapse.

Indexed as

Immunoglobulin Light-chain AmyloidosisImmunoglobulin Light ChainsAntineoplastic Combined Chemotherapy ProtocolsBortezomibHematopoietic Stem Cell TransplantationHumansMultiple MyelomaBortezomibImmunoglobulin Light ChainsAutologus stem cells transplantLCDDLight chain deposition diseaseMGRSMonoclonal gammopathyPlasma cells

Identifiers

PMID39196376
PMCPMC12052853

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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.