Evidence map›Paper›PMID 29925902›Full record

ArticleLeukemia2018

Characterisation of immunoparesis in newly diagnosed myeloma and its impact on progression-free and overall survival in both old and recent myeloma trials.

Jennifer L J Heaney, John P Campbell, Gulnaz Iqbal, David Cairns, Alex Richter, J Anthony Child, Walter Gregory, Graham Jackson, Martin Kaiser, Roger Owen and 4 more

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 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
–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

41 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Jennifer L J HeaneyInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
John P CampbellInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Gulnaz IqbalUniversity of Warwick, Warwick, UK.
David CairnsUniversity of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0002-2338-0179
Alex RichterInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
J Anthony ChildUniversity of Leeds, Leeds, UK.
Walter GregoryUniversity of Leeds, Leeds, UK.
Graham JacksonUniversity of Newcastle, Newcastle, UK.
Martin KaiserInstitute of Cancer Research, London, UK.
Roger OwenSt James's University Hospital, Leeds, UK.
Faith DaviesUniversity of Arkansas for Medical Sciences, Little Rock, AR, USA.
Gareth MorganUniversity of Arkansas for Medical Sciences, Little Rock, AR, USA.
Janet DunnUniversity of Warwick, Warwick, UK.
Mark T DraysonInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK. M.T.Drayson@bham.ac.uk.

Funding

Medical Research Council G0100132
6 · The paper itself

Abstract

We measured immunosuppression at myeloma diagnosis and assessed the impact on survival in 5826 UK myeloma trial patients. Polyclonal immunoglobulin levels were below normal in 85% of patients and above normal in only 0.4% of cases for IgA, 0.2% for IgM and no cases for IgG. Immunoparesis had a greater impact in recent trials: median overall survival (OS) was up to 3 years longer for patients without immunoparesis compared to the old trials, less than 1 year longer. Median progression-free survival (PFS) was 39%, 36% and 57% longer for patients with normal IgG, IgA and IgM levels, respectively. The depth of IgM suppression, but not the depth of IgG or IgA suppression, was prognostic for survival: the most severely suppressed IgM tertile of patients OS was 0.9 years shorter than those in the top tertile, and 2.6 years shorter than OS of those with normal IgM levels (p = .007). The degree of suppression of polyclonal IgM levels below normal was associated with worse PFS (p = .0002). Infection does not appear to be the main mechanism through which immunoparesis affects survival. We hypothesise that IgM immunoparesis impacts through a combination of being associated with more aggressive disease and reduced immune surveillance against relapse.

Indexed as

AgedDisease ProgressionFemaleFollow-Up StudiesHumansImmune ToleranceImmunoglobulinsMaleMultiple MyelomaPrognosisRetrospective StudiesSurvival RateImmunoglobulins

Identifiers

PMID29925902
PMCPMC6087716

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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.