Evidence map›Paper›PMID 33149136›Full record

Trial reportBlood cancer journal2020

Anti-bacterial antibodies in multiple myeloma patients at disease presentation, in response to therapy and in remission: implications for patient management.

Ilaria J Chicca, Jennifer L J Heaney, Gulnaz Iqbal, Janet A Dunn, Stella Bowcock, Guy Pratt, Kwee L Yong, Timothy D Planche, Alex Richter, Mark T Drayson

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood cancer journal, 2020. 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
1.1field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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

10 authors at 6 institutions in 1 country.

Ilaria J ChiccaInstitute of Immunology and Immunotherapy, Clinical Immunology Service, University of Birmingham, Birmingham, UK.ORCID 0000-0002-3191-8645
Jennifer L J HeaneyInstitute of Immunology and Immunotherapy, Clinical Immunology Service, University of Birmingham, Birmingham, UK.
Gulnaz IqbalWarwick Clinical Trial Unit, University of Warwick, Coventry, UK.
Janet A DunnWarwick Clinical Trial Unit, University of Warwick, Coventry, UK.
Stella BowcockKing's College Hospital NHS Trust, London, UK.ORCID 0000-0002-8195-8960
Guy PrattUniversity Hospital Birmingham NHS Trust, Birmingham, UK.
Kwee L YongDepartment of Haematology, UCL Cancer Institute, London, UK.
Timothy D PlancheSt. George's Hospital, University of London, Department of Medical Microbiology, Tooting, London, UK.ORCID 0000-0002-0263-0888
Alex RichterInstitute of Immunology and Immunotherapy, Clinical Immunology Service, University of Birmingham, Birmingham, UK.
Mark T DraysonInstitute of Immunology and Immunotherapy, Clinical Immunology Service, University of Birmingham, Birmingham, UK. M.T.Drayson@bham.ac.uk.ORCID 0000-0002-1528-7564
University of Birmingham · GBUniversity of Warwick · GBCRUK Lung Cancer Centre of Excellence · GBKing's College Hospital · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of London · GB

Funding

Department of Health 08/116/69Department of Health 14/24/04DH | NIHR | Efficacy and Mechanism Evaluation Programme (NIHR Efficacy and Mechanism Evaluation Programme) 14/24/04DH | NIHR | Health Technology Assessment Programme (NIHR Health Technology Assessment Programme) 08/116/69
6 · The paper itself

Abstract

Multiple myeloma (MM) is associated with increased risk of infection, but little is known regarding antibody levels against specific bacteria. We assessed levels of polyclonal immunoglobulin and antibacterial antibodies in patients recruited to the TEAMM trial, a randomised trial of antibiotic prophylaxis at the start of anti-myeloma treatment. Polyclonal IgG, IgA and IgM levels were below the reference range in 71%, 83% and 90% of 838 MM patients at diagnosis. Anti-vaccine targeted tetanus toxoid antibodies were protective in 95% of 193 healthy controls but only 41% of myeloma patients. In healthy controls, protective antibodies against 6/12 pneumococcal serotypes, haemophilus and meningococcus A were present in 67%, 41% and 56% compared to just 15%, 21% and 17% of myeloma patients. By 1 year, myeloma patients IgG levels had recovered for 57% of patients whilst the proportion with protective levels of IgG against thymus-dependent protein antigen tetanus toxoid had changed little. In contrast the proportions of patients with protective levels against thymus independent polysaccharide antigens pneumococcus, haemophilus and meningococcus had fallen from 15 to 7%, 21 to 0% and 17 to 11%. Findings highlight the need for strategies to protect patients against bacterial infections during therapy and vaccination programmes during remission.

Indexed as

AgedAnti-Bacterial AgentsAntibodies, BacterialBacterial InfectionsDouble-Blind MethodFemaleHumansMaleMiddle AgedMultiple MyelomaAnti-Bacterial AgentsAntibodies, Bacterial

Identifiers

PMID33149136
PMCPMC7642409
OpenAlexW3095052242

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.