Evidence map›Paper›PMID 30873378›Full record

ArticleFrontiers in oncology2019

Apixaban for Primary Prevention of Venous Thromboembolism in Patients With Multiple Myeloma Receiving Immunomodulatory Therapy.

Robert Frank Cornell, Samuel Z Goldhaber, Brian G Engelhardt, Javid Moslehi, Madan Jagasia, Daryl Patton, Shelton Harrell, Robert Hall, Houston Wyatt, Greg Piazza

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02958969 (Apixaban for Primary Prevention of Venous Thromboembolism in Patients With Multiple Myeloma Receiving Immunomodulatory Therapy), which is not on this map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
4.6field-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.

NCT02958969 phase4completednot on this map

Apixaban for Primary Prevention of Venous Thromboembolism in Patients With Multiple Myeloma Receiving Immunomodulatory Therapy

TypeinterventionalSponsorGregory PiazzaRan2018 to 2019Enrolled50ConditionsVenous Thromboembolism, Multiple MyelomaArmsApixaban
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 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

10 authors at 3 institutions in 1 country.

Robert Frank CornellDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Samuel Z GoldhaberDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School Boston, MA, United States.
Brian G EngelhardtDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Javid MoslehiCardio-Oncology Program, Vanderbilt University Medical Center Nashville, TN, United States.
Madan JagasiaDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Daryl PattonVanderbilt Institute for Clinical and Translational Research Nashville, TN, United States.
Shelton HarrellDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Robert HallDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Houston WyattDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center Nashville, TN, United States.
Greg PiazzaDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School Boston, MA, United States.
Vanderbilt University Medical Center · USBrigham and Women's Hospital · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunomodulatory drugs (IMiDs), including thalidomide, lenalidomide, and pomalidomide, have improved survival of patients with multiple myeloma (MM). However, these therapies are associated with an increased risk of venous thromboembolism (VTE). Apixaban has been approved for treatment of acute VTE and for risk reduction of recurrent VTE following initial therapy. In this phase IV single-arm study (NCT02958969), we aim to prospectively evaluate the safety and efficacy of apixaban for primary prevention of VTE in patients with MM. The primary efficacy objective of this trial is to determine the rate of symptomatic VTE, including deep vein thrombosis (DVT) and pulmonary embolism (PE), over 6 months. The primary safety objective is to determine the rate of major bleeding in MM patients receiving apixaban prophylaxis. If proven safe and effective, apixaban will emerge as a promising option for oral VTE prophylaxis in MM patients.

Indexed as

anticoagulation (AC)Apixaban (Eliquis®)immunomodualtorsmyelomavenous thomboembolism

Identifiers

PMID30873378
PMCPMC6401636
OpenAlexW2916552441

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.