Evidence map›Paper›PMID 42231132›Full record

ArticleThe oncologist2026

Reporting of primary endpoint and associated spin in randomized myeloma trials.

Mitch Singstock, Abul Hasan Shadali Abdul Khader, Cole Wayant, Mackenzie Lemieux, Maria Mainou, Ghulam Rehman Mohyuddin

Abstract read
In one paragraph

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

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0citing papers in PubMed
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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

6 authors.

Mitch SingstockDepartment of Internal Medicine, University of Utah, Salt Lake City, UT, 84112, United States.ORCID 0000-0002-2657-7831
Abul Hasan Shadali Abdul KhaderDepartment of Internal Medicine, Mercy Catholic Medical Center, PA, 19023, United States.ORCID 0000-0001-5628-3829
Cole WayantDivision of Medical Oncology, University of Colorado Anschutz, Denver, CO, 80045, United States.ORCID 0000-0001-8829-8179
Mackenzie LemieuxDepartment of Internal Medicine, University of Utah, Salt Lake City, UT, 84112, United States.ORCID 0000-0001-6015-8668
Maria MainouClinical Research and Evidence Based Medicine Unit, Aristotle University of Thessaloniki, Thessaloniki, 54124, Greece.ORCID 0000-0002-5775-2241
Ghulam Rehman MohyuddinDivision of Hematology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, 84112, United States.ORCID 0000-0001-6464-783X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOncology clinical trials, regardless of success in meeting their primary endpoint, often suffer from spin-the misrepresentation of research findings. Despite dramatic improvements in myeloma outcomes, numerous recent myeloma trials have failed to meet their primary endpoints while others have amplified marginally positive findings. A thorough evaluation of reporting practices and spin in myeloma randomized controlled trials (RCTs) is needed. MATERIALS AND

methodsWe performed a cross-sectional analysis of myeloma RCTs that began enrollment in January 2015 or later, with final search conducted in March 2025. Reporting of prespecified primary endpoints and sample size calculations was abstracted. Two reviewers screened for the presence of spin, defined as at least one reporting practice that could mislead readers by emphasizing benefit or minimizing unfavorable findings. Multivariable logistic regression was used to determine factors associated with spin. The methods were registered on the Open Science Framework.

resultsOf 82 screened studies, 71 RCTs were included. The prespecified primary endpoint was statistically significant in 46 trials (64.8%). Sample size calculations were reported in 51 trials (71.8%), and conclusions aligned with primary endpoint results in 63 trials (88.7%). Spin occurred in 25 trials (35.2%), most commonly through optimistic language and emphasis on secondary/subgroup findings. In multivariable analysis, meeting the prespecified primary endpoint was associated with lower odds of spin (adjusted odds ratio [OR] = 0.15; 95% CI, 0.03-0.70; P = .016).

conclusionSpin affected one-third of contemporary myeloma RCTs and was strongly associated with nonsignificant primary endpoints, highlighting the need for primary endpoint-aligned interpretation and transparent sample size reporting.

Indexed as

Endpoint DeterminationMultiple MyelomaRandomized Controlled Trials as TopicResearch DesignCross-Sectional StudiesHumansmultiple myelomaprimary endpointrandomized controlled trialsresearch integrityresearch reportingsample size calculationspintrial interpretation

Identifiers

PMID42231132
PMCPMC13275311

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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.