Evidence map›Paper›PMID 39790465›Full record

ArticleBritish journal of cancer research2024

Seeking Amyloidosis Very Early: Free light Chain Differentials and IGLV Gene Use as Screening Variables for Light-chain Amyloidosis in λ Monoclonal Gammopathies.

Ping Zhou, Mahesh M Mansukhani, Raymond Yeh, Jiesheng Lu, Hongai Xia, Lahari Koganti, Jiuhong Pang, Denis Toskic, Stephanie Scalia, Xun Ma and 4 more

Abstract read
In one paragraph

Article in British journal of cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. An updated AL-base reveals ranked enrichment of immunoglobulin light chain variable genes in AL amyloidosis.Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis · 2025
    Article
  3. Article
  4. Review
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

14 authors.

Ping ZhouThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.
Mahesh M MansukhaniColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Raymond YehColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Jiesheng LuColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Hongai XiaColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Lahari KogantiColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Jiuhong PangColumbia University Laboratory of Personalized Genomic Medicine, Department of Pathology & Cell Biology, Columbia University Medical Center, New York, NY, USA.
Denis ToskicThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.
Stephanie ScaliaThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.
Xun MaThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.
Nancy Coady LyonsDivision of Hematology-Oncology, Department of Medicine, Tufts Medical Center, Boston, MA, USA.
Teresa FogarenThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.
Cindy VargaAtrium Health Levine Cancer Institute, Charlotte, NC, USA.
Raymond L ComenzoThe John Conant Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA, USA.

Funding

Screening for AL Amyloidosis in Smoldering Multiple MyelomaR01CA279808 · NCI · TUFTS MEDICAL CENTER · PI Raymond Luke Comenzo · 2024 to 2026
$2.3M
Screening to Improve Survival in AL AmyloidosisR21AG070502 · NIA · TUFTS MEDICAL CENTER · PI COMENZO, RAYMOND LUKE, LENTZSCH, SUZANNE · 2020 to 2021
$515k
NCI NIH HHS R01 CA279808NIA NIH HHS R21 AG070502
6 · The paper itself

Abstract

Background: Early diagnosis of systemic light-chain amyloidosis (AL) is needed because 25% of patients die within months of diagnosis. In patients with monoclonal gammopathy of undetermined significance (MGUS) or smoldering multiple myeloma (SMM) of the λ isotype, we explored the use of 2 screening variables: a free light chain difference of 23mg/L between λ and k and presence of IGLV genes that occur more frequently in AL. Methods: Patients contacted us and we sent HIPAA release and consent forms for discussion by phone. Their physicians were not involved. We enrolled patients with λ MGUS or SMM who met the FLC criteria with no prior biopsies showing amyloid. They sent us blood or marrow specimens for IGLV gene amplification by RT-PCR; we also assessed the feasibility of next generation sequencing (NGS) for IGLV genes. We informed patients and their physicians of results suggesting further evaluation for AL. Results: We enrolled 21 patients, 19 SMM and 2 MGUS, receiving blood (n=21) or marrow (n=5) specimens. We identified IGLV genes in 86% (18/21) of cases. Four of the 18 IGLV genes were not AL-related and 3 of these 4 progressed to myeloma requiring therapy; the 4th was screened for amyloid and was negative. Fourteen patients with AL-related genes had comprehensive evaluations and two with SMM had AL. RT-PCR and NGS identified the AL-related LV2-14 in those two and also the monoclonal IGLV genes from all of the marrow but not the peripheral blood samples. Conclusion: We concluded that these variables may be useful in screening for AL in λ MGUS and SMM patients and acquired support for a small multi-center study employing marrow samples only.

Indexed as

AL amyloidosisIGLV genesmonoclonal gammopathiesnext generation sequencing

Identifiers

PMID39790465
PMCPMC11711923

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.