Evidence map›Paper›PMID 26771810›Full record

ArticleBlood cancer journal2016

Carfilzomib and the cardiorenal system in myeloma: an endothelial effect?

A Rosenthal, J Luthi, M Belohlavek, K M Kortüm, F Mookadam, A Mayo, R Fonseca, P L Bergsagel, C B Reeder, J R Mikhael and 1 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
9.3field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 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

11 authors at 1 institution in 1 country.

A RosenthalDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
J LuthiDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
M BelohlavekDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
K M KortümDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
F MookadamDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
A MayoDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
R FonsecaDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
P L BergsagelDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
C B ReederDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
J R MikhaelDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
A K StewartDivision of Hematology Oncology, Mayo Clinic Arizona, Scottsdale, AZ, USA.
Mayo Clinic in Arizona · US

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

Carfilzomib (Cfz) has been associated with an ~5% incidence of unexplained and unpredictable cardiovascular toxicity in clinical trials. We therefore implemented a detailed, prospective, clinical cardiac and renal evaluation of 62 Cfz-treated myeloma patients, including serial blood pressure (BP), creatinine, troponin, NT-proBNP and pre- and post-treatment echocardiograms, including ejection fraction (EF), average global longitudinal strain and compliance. Pre-treatment elevations in NT-proBNP and BP, as well as abnormal cardiac strain were common. A rise in NT-proBNP occurred frequently post-treatment often without corresponding cardiopulmonary symptoms. A rise in creatinine was common, lessened with hydration and often reversible. All patients had a normal EF pre-treatment. Five patients experienced a significant cardiac event (four decline in EF and one myocardial infarction), of which 2 (3.2%) were considered probably attributable to Cfz. None were rechallenged with Cfz. The ideal strategy for identifying patients at risk for cardiac events, and parameters by which to monitor for early toxicity have not been established; however, it appears baseline echocardiographic testing is not consistently predictive of toxicity. The toxicities observed suggest an endothelial mechanism and further clinical trials are needed to determine whether or not this represents a class effect or is Cfz specific.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCardiotoxicityFemaleHeart DiseasesHumansKidney DiseasesMaleMiddle AgedMultiple MyelomaNatriuretic Peptide, BrainOligopeptidesPeptide FragmentsProteasome InhibitorsBiomarkerscarfilzomibNatriuretic Peptide, BrainOligopeptidesPeptide Fragmentspro-brain natriuretic peptide (1-76)Proteasome Inhibitors

Identifiers

PMID26771810
PMCPMC4742629
OpenAlexW2234403337

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.