Evidence map›Paper›PMID 42645376›Full record

Observational studyCurrent oncology (Toronto, Ont.)2026

Incidence and Associated Risk Factors in the Development of Carfilzomib-Induced Cardiovascular Toxicity.

Noor Lad, Jayda Esplund, Dennis Grauer, Shebli Atrash, Prerna Mewawalla, Tejaswi Gadela, Charles Porter, Muhammad Mushtaq, Jeries Kort, Donald C Moore and 3 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Current oncology (Toronto, Ont.), 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

13 authors.

Noor LadDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Jayda EsplundDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Dennis GrauerDepartment of Pharmacy Practice, The University of Kansas School of Pharmacy, Kansas City, KS 66047, USA.
Shebli AtrashLevine Cancer Center, Atrium Health, Wake Forest University School of Medicine, Charlotte, NC 28262, USA.ORCID 0000-0003-4547-7534
Prerna MewawallaDivision of Hematology and Cellular Therapy, AHN Cancer Institute, Allegheny Health Network, Pittsburgh, PA 15212, USA.ORCID 0009-0008-7464-6898
Tejaswi GadelaDivision of Hematology and Cellular Therapy, AHN Cancer Institute, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Charles PorterDepartment of Cardiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.ORCID 0000-0001-8820-9279
Muhammad MushtaqDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.
Jeries KortDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0001-9182-3931
Donald C MooreLevine Cancer Center, Atrium Health, Wake Forest University School of Medicine, Charlotte, NC 28262, USA.
Al-Ola AbdallahDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-6603-185X
Zahra MahmoudjafariDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.ORCID 0000-0002-3168-2521
Jordan SnyderDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66205, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarfilzomib, a second-generation proteasome inhibitor, is widely used in multiple myeloma (MM) treatment but has been associated with cardiovascular adverse events (CVAEs). Real-world data evaluating the incidence and risk factors are limited.

methodsWe conducted a multicenter retrospective cohort study of 385 adult MM patients treated with carfilzomib between January 2020 and August 2024 at three U.S. institutions. The primary objective of this study was to determine the incidence of carfilzomib-associated CVAEs. The secondary objectives included the identification of risk factors, characterization of cardiovascular events, and time-to-onset analysis.

resultsCarfilzomib-associated CVAEs occurred in 25 patients (6.5%). The median time to event was 114 days. Heart failure was the most common manifestation (86%), followed by arrhythmias (32%) and acute coronary syndromes (8%). Patients with baseline heart failure had a significantly increased risk of CVAEs (HR 1.61,

conclusionCarfilzomib-associated CVAEs were infrequent but clinically meaningful in this multicenter cohort. These findings support consideration of a risk-adapted cardio-oncology approach, particularly in patients with pre-existing cardiac dysfunction, where closer surveillance and early intervention may help mitigate clinically significant cardiotoxicity.

Indexed as

CardiotoxicityCardiovascular DiseasesMultiple MyelomaOligopeptidesAgedFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesRisk FactorscarfilzomibOligopeptidescardio-oncologycardiotoxicitycardiovascular adverse eventscarfilzomibmultiple myelomarisk factors

Identifiers

PMID42645376
PMCPMC13511659

What OpenQuestion holds

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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.