Evidence map›Paper›PMID 28663581›Full record

ArticleLeukemia2018

Heavy+light chain monitoring correlates with clinical outcome in multiple myeloma patients.

M Michallet, C Chapuis-Cellier, T Dejoie, C Lombard, H Caillon, M Sobh, P Moreau, M Attal, H Avet-Loiseau

Abstract read
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. [Minimal residual disease assessment and progress in multiple myeloma].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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  16. Recombinant Antibodies to Arm Cytotoxic Lymphocytes in Cancer Immunotherapy.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2017
    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

9 authors.

M MichalletDepartment of Hematology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Lyon, France.
C Chapuis-CellierImmunological Laboratory, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Lyon, France.
T DejoieBiochemistry Laboratory, University Hospital Nantes, Nantes, France.
C LombardImmunological Laboratory, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Lyon, France.
H CaillonBiochemistry Laboratory, University Hospital Nantes, Nantes, France.
M SobhDepartment of Hematology, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Lyon, France.
P MoreauDepartment of Hematology, Nantes University Hospital, Nantes, France.
M AttalInstitut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.
H Avet-LoiseauInstitut Universitaire du Cancer de Toulouse-Oncopole, Unite de Genomique du Myelome, Toulouse, France.

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
NCI NIH HHS P50 CA100707
6 · The paper itself

Abstract

Novel anti-myeloma agents have improved patient response rates, which are historically based on reductions of the M-protein. These methods can be inaccurate for quantifying M-proteins at low concentrations. We compared the consistency and clinical impact of response assignment by electrophoretic and heavy+light chain (HLC) immunoassays post-consolidation in 463 newly diagnosed patients. The two methods gave similar assignments in patients with partial (PR; 79% agreement) or complete response (⩾CR; 92%). However, in patients achieving very good PR (VGPR) there was poor concordance between methods (45%). Median progression-free survival (PFS) for standard VGPR patients was 34.5 months; HLC responses stratified these patients further into PR, VGPR and ⩾CR, with median PFS of 21.3, 28.9 months and not reached, respectively; P<0.001. At this time, abnormal HLC ratios had better concordance with multiparametric flow cytometry (sensitivity 10

Indexed as

AdultAgedFemaleHumansImmunoelectrophoresisImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsMaleMiddle AgedMultiple MyelomaMyeloma ProteinsPrognosisProgression-Free SurvivalImmunoglobulin Heavy ChainsImmunoglobulin Light Chainsmultiple myeloma M-proteinsMyeloma Proteins

Identifiers

PMID28663581
PMCPMC5808078

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.