Evidence map›Paper›PMID 38499538›Full record

ArticleBlood cancer journal2024

Progression free survival of myeloma patients who become IFE-negative correlates with the detection of residual monoclonal free light chain (FLC) by mass spectrometry.

H V Giles, M T Drayson, B Kishore, C Pawlyn, M Kaiser, G Cook, R de Tute, R G Owen, D Cairns, T Menzies and 4 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

14 authors at 7 institutions in 2 countries.

H V GilesUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK. Hannah.giles@uhb.nhs.uk.ORCID 0000-0001-6292-3802
M T DraysonUniversity of Birmingham, Birmingham, UK.ORCID 0000-0002-1528-7564
B KishoreUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
C PawlynThe Institute of Cancer Research, London and The Royal Marsden Hospital, London, UK.ORCID 0000-0002-7190-0028
M KaiserThe Institute of Cancer Research, London and The Royal Marsden Hospital, London, UK.ORCID 0000-0002-3677-4804
G CookLeeds Cancer Research UK Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID 0000-0003-1717-0412
R de TuteHaematological Malignancy Diagnostic Service, Leeds Teaching Hospitals Trust, Leeds, UK.
R G OwenHaematological Malignancy Diagnostic Service, Leeds Teaching Hospitals Trust, Leeds, UK.
D CairnsLeeds Cancer Research UK Institute of Clinical Trials Research, University of Leeds, Leeds, UK.ORCID 0000-0002-2338-0179
T MenziesLeeds Cancer Research UK Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
F E DaviesMyeloma Research Program, Perlmutter Cancer, NYU Langone Health, New York, USA.
G J MorganMyeloma Research Program, Perlmutter Cancer, NYU Langone Health, New York, USA.
G Pratt *University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.ORCID 0000-0002-6937-2852
G H Jackson *Department of Haematology, University of Newcastle, Newcastle upon Tyne, UK.
University Hospitals Birmingham NHS Foundation Trust · GBUniversity of Leeds · GBInstitute of Cancer Research · GBLeeds Teaching Hospitals NHS Trust · GBNYU Langone Health · USNewcastle University · GBUniversity of Birmingham · GB

Funding

British Society for Haematology (BSH) 36374/ESR2020
6 · The paper itself

Abstract

Deeper responses are associated with improved survival in patients being treated for myeloma. However, the sensitivity of the current blood-based assays is limited. Historical studies suggested that normalisation of the serum free light chain (FLC) ratio in patients who were negative by immunofixation electrophoresis (IFE) was associated with improved outcomes. However, recently this has been called into question. Mass spectrometry (MS)-based FLC assessments may offer a superior methodology for the detection of monoclonal FLC due to greater sensitivity. To test this hypothesis, all available samples from patients who were IFE negative after treatment with carfilzomib and lenalidomide-based induction and autologous stem cell transplantation (ASCT) in the Myeloma XI trial underwent FLC-MS testing. FLC-MS response assessments from post-induction, day+100 post-ASCT and six months post-maintenance randomisation were compared to serum FLC assay results. Almost 40% of patients had discordant results and 28.7% of patients with a normal FLC ratio had residual monoclonal FLC detectable by FLC-MS. FLC-MS positivity was associated with reduced progression-free survival (PFS) but an abnormal FLC ratio was not. This study demonstrates that FLC-MS provides a superior methodology for the detection of residual monoclonal FLC with FLC-MS positivity identifying IFE-negative patients who are at higher risk of early progression.

Indexed as

Hematopoietic Stem Cell TransplantationMultiple MyelomaHumansImmunoglobulin Light ChainsMass SpectrometryProgression-Free SurvivalRandomized Controlled Trials as TopicTransplantation, AutologousImmunoglobulin Light Chains

Identifiers

PMID38499538
PMCPMC10948753
OpenAlexW4392897332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.