Evidence map›Paper›PMID 41743685›Full record

ArticleDiscover medicine2026

Clinical factors associated with venous thromboembolism in multiple myeloma patients treated with daratumumab.

Naveen G Subramanian, Fleur M Aung, Zachary E Hunzeker, Krina K Patel, Hans C Lee, Shida Jin, Elliana Young, Roland L Bassett, Cristhiam M Rojas Hernandez

Abstract read
In one paragraph

Article in Discover medicine, 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

9 authors.

Naveen G SubramanianInternal Medicine Residency, UTHealth McGovern Medical School, Houston, TX USA.
Fleur M AungDepartment of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Zachary E HunzekerInternal Medicine Residency, UTHealth McGovern Medical School, Houston, TX USA.
Krina K PatelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Hans C LeeDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Shida JinEnterprise Integration & Development, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Elliana YoungEnterprise Data Engineering & Analytics, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Roland L BassettDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX USA.
Cristhiam M Rojas HernandezSection of Benign Hematology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd. Suite 1464, Houston, TX 77030 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Venous thromboembolism (VTE) is a common cause of morbidity and mortality in patients with multiple myeloma (MM). There has been little evidence investigating the factors associated with VTE during therapy with daratumumab-containing regimens. Objectives: Our study examined the association of different clinical, medication- and procedure-related factors on the development of VTE events. Methods: We performed a retrospective chart review of multiple myeloma patients treated at our institution with daratumumab-containing regimens and who developed VTE within 12 months of starting daratumumab. We collected the information on clinical factors, cancer therapy, antithrombotic medications, and central venous access procedures during the observation period. A univariate logistic regression was done first to identify variables associated with VTE, after which those variables were entered into a multivariate analysis. Results: Among patients with MM who received a daratumumab-containing regimen, the incidence of VTE was 9.6% at 12 months from the initiation of daratumumab. We found that the number of PICC line insertions and the presence of multiple medical comorbidities were associated with VTE development. Conclusions: We conclude that VTE is frequent during therapy for MM, particularly in the presence of certain risk factors such as use of multiple PICC line insertions and recent infections. Our observations do not imply causality and limited by the retrospective design, small number of VTE events and lack of time-to-event analysis in the study.

Indexed as

Multiple myelomaNatural language processingRiskThromboprophylaxisVenous thromboembolism

Identifiers

PMID41743685
PMCPMC12929259

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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.