Evidence map›Paper›PMID 38481947›Full record

ArticleTherapeutic advances in hematology2024

A phase I trial of pevonedistat in combination with ruxolitinib for the treatment of myelofibrosis.

Tim Kong, Nicole Gaudin, Karyn Gordon, Maggie J Cox, Amy W Zhou, Stephen T Oh

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Therapeutic advances in hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03386214 (Pevonedistat in Combination With Ruxolitinib for Treatment of Patients With Myelofibrosis), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 21% 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.

NCT03386214 phase1terminatednot on this map

Pevonedistat in Combination With Ruxolitinib for Treatment of Patients With Myelofibrosis

TypeinterventionalSponsorWashington University School of MedicineRan2018 to 2021Enrolled8ConditionsMyelofibrosesArmsPevonedistat, Ruxolitinib, Peripheral blood draw, Skin biopsy
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Novel Therapies in Myeloproliferative Neoplasms: Beyond JAK Inhibitor Monotherapy.Journal of immunotherapy and precision oncology · 2021
    Review
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 at 1 institution in 1 country.

Tim KongDivision of Hematology, Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Nicole GaudinDivision of Hematology, Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Karyn GordonDivision of Hematology, Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Maggie J CoxDivision of Hematology, Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Amy W ZhouDivision of Hematology, Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
Stephen T OhDivision of Hematology, Department of Medicine, Washington University School of Medicine, 660 S. Euclid Avenue, Campus Box 8125, St Louis, MO 63110, USA.ORCID https://orcid.org/0000-0002-8564-5400
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
NCI NIH HHS P30 CA091842
6 · The paper itself

Abstract

Janus kinase 2 (JAK2) inhibitors such as ruxolitinib have become standard-of-care therapy for patients with myeloproliferative neoplasms (MPNs); however, activation of alternate oncogenic pathways including nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) has limited durable response as single-agent therapy. With the rationale of targeting both pathways, we conducted a phase I dose escalation trial of pevonedistat in combination with ruxolitinib for the treatment of patients with myelofibrosis (NCT03386214). The primary objective was to assess the safety and tolerability of combination therapy with additional objectives of treatment efficacy and alterations of biomarkers. There were no dose-limiting toxicities observed with most adverse events being limited to grades 1/2. In secondary measures, anemia response was observed in two patients. Pro-inflammatory cytokines and iron parameters were longitudinally assessed, which revealed suppression of interleukin-6 and interferon-gamma in a dose-dependent manner across a subset of patients. These results suggest that combination therapy targeting both JAK2 and NFκB may hold clinical merit for MPN patients.

Indexed as

clinical trialJAK2MLN4924myeloproliferative neoplasmsNFκBpevonedistatruxolitinib

Identifiers

PMID38481947
PMCPMC10935761
OpenAlexW4392751918

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.