Evidence map›Paper›PMID 42162568›Full record

ArticleBritish journal of haematology2026

Recognising disease progression in MGUS and smouldering myeloma: Biomarkers, symptom monitoring and imaging.

Aidan Haslam, Gulnaz Iqbal, Mark Drayson, Guy Pratt, Kwee Yong, Janet Dunn, Catherine Atkin, Chris Bunce, Donna Howe, Stella Bowcock

Abstract readMulticenter Study
In one paragraph

Article in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Aidan HaslamSchool of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Birmingham, UK.ORCID https://orcid.org/0000-0002-4975-3156
Gulnaz IqbalWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK.
Mark DraysonSchool of Infection, Inflammation and Immunology, College of Medicine and Health, Birmingham, UK.
Guy PrattDepartment of Haematology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Kwee YongUniversity College London Cancer Institute, University College London, London, UK.
Janet DunnWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK.
Catherine AtkinSchool of Infection, Inflammation and Immunology, College of Medicine and Health, Birmingham, UK.ORCID https://orcid.org/0000-0003-0596-8515
Chris BunceSchool of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Birmingham, UK.
Donna HoweWarwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK.
Stella BowcockDepartment of Haematology, King's College Hospital NHS Foundation Trust, London, UK.

Funding

Blood Cancer UK MRL02.23Myeloma UK MUK2021.ED03National Institute for Health and Care Research 14/24/04
6 · The paper itself

Abstract

The Tackling Early Morbidity and Mortality in Myeloma trial (TEAMM) trial recruited 977 newly diagnosed myeloma patients from 93 UK hospitals to assess the advantages and disadvantages of prophylactic antibiotics for the first 12 weeks. This paper analyses the 133 (14%) patients who had previously known precursor disease including monoclonal gammopathy of undetermined significance (MGUS) and smouldering myeloma (SMM), reporting the relative importance of blood-based biomarkers, imaging findings and symptoms in their management. Prior to progression with active myeloma, patients with precursor conditions had symptoms for five times longer than patients with no diagnosed precursor phase. Although only 29% of patients reported new myeloma-related symptoms developing after their first haematology appointment, 70% had a significant rise in paraprotein levels prior to progression. Likewise, risk scores for both MGUS and SMM increased prior to progression. Fractures occurred in 25% of patients despite being monitored for precursor disease. These fractures were difficult to predict as biomarkers lacked specificity and only 40% of patients reported back pain in combination with vertebral fractures. This study highlights the ongoing challenge of promptly recognising disease progression when using patient-reported symptoms and monoclonal immunoglobulin monitoring.

Indexed as

Monoclonal Gammopathy of Undetermined SignificanceSmoldering Multiple MyelomaAgedBiomarkersBiomarkers, TumorDisease ProgressionFemaleHumansMaleMiddle AgedBiomarkersBiomarkers, Tumorbiomarkerdisease progressionimagingmonitoringmonoclonal gammopathy of undetermined significance (MGUS)myelomasmouldering myelomasymptom

Identifiers

PMID42162568
PMCPMC13267434

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.