Evidence map›Paper›PMID 34059488›Full record

Trial reportClinical lymphoma, myeloma & leukemia2021

Sex Differences in Multiple Myeloma Biology but not Clinical Outcomes: Results from 3894 Patients in the Myeloma XI Trial.

Sarah Bird, David Cairns, Tom Menzies, Kevin Boyd, Faith Davies, Gordon Cook, Mark Drayson, Walter Gregory, Matthew Jenner, John Jones and 5 more

Open access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Clinical lymphoma, myeloma & leukemia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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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

15 authors at 9 institutions in 3 countries.

Sarah BirdThe Institute of Cancer Research, London; The Royal Marsden Hospital, London.
David CairnsClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds.
Tom MenziesClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds.
Kevin BoydThe Institute of Cancer Research, London; The Royal Marsden Hospital, London.
Faith DaviesPerlmutter Cancer Center, NY Langone Health, New York, USA.
Gordon CookClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds.
Mark DraysonClinical Immunology, University of Birmingham, Birmingham.
Walter GregoryClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds.
Matthew JennerUniversity Hospital Southampton NHS Foundation Trust, Southampton.
John JonesThe Institute of Cancer Research, London.
Martin KaiserThe Institute of Cancer Research, London; The Royal Marsden Hospital, London.
Roger OwenSt James's University Hospital, Leeds.
Graham JacksonDepartment of Haematology, Newcastle University, Newcastle.
Gareth MorganPerlmutter Cancer Center, NY Langone Health, New York, USA.
Charlotte PawlynThe Institute of Cancer Research, London; The Royal Marsden Hospital, London. Electronic address: charlotte.pawlyn@icr.ac.uk.
Royal Marsden Hospital · GBUniversity of Leeds · GBInstitute of Cancer Research · CANewcastle University · GBNYU Langone Health · USNYU Langone’s Laura and Isaac Perlmutter Cancer CenterSt James's University Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Birmingham · GB

Funding

Cancer Research UK 25447Cancer Research UK 29957
6 · The paper itself

Abstract

backgroundSex differences in the incidence and outcomes of several cancers are well established. Multiple myeloma (MM) is a malignant plasma cell dyscrasia accounting for 2% of all new cancer cases in the UK. There is a clear sex disparity in MM incidence, with 57% of cases in males and 43% in females. The mechanisms behind this are not well understood and the impact of sex on patient outcomes has not been thoroughly explored. PATIENTS AND

methodsWe investigated the association of sex with baseline disease characteristics and outcome in 3894 patients recruited to the phase III UK NCRI Myeloma XI trial, in which treatment exposure to lenalidomide predominated.

resultsFemales were significantly more likely to have the molecular lesions t(14;16) and del(17p) and were more likely to meet the cytogenetic classification of high-risk (HiR) or ultra-high-risk disease (UHiR). There was no difference in progression-free survival (PFS) or overall survival (OS) between the sexes in the overall population.

conclusionOur data suggest that the genetic lesions involved in the initiation and progression of MM may be different between the sexes. Although females were more likely to have the poor prognosis lesions t(14;16) and del(17p), and were more likely to be assessed as having HiR or UHiR disease, this was not associated with reduced PFS or OS. In female patients the trial treatment may have been able to overcome some of the adverse effects of high-risk cytogenetic lesions. MicroAbstract Multiple myeloma (MM) is more common in males compared to females but the reasons behind this are not well understood and the impact of sex on patient outcomes is unclear. This study demonstrates fundamental differences in genetic lesions underlying the biology of MM between males and females. However, we found that progression-free survival and overall survival were the same in both sexes.

Indexed as

Sex CharacteristicsAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansMaleMultiple MyelomaTreatment OutcomeClinical trialsImmunomodulatory drugs+myelomaSex differences

Identifiers

PMID34059488
PMCPMC8528179
OpenAlexW3158356424

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.