Evidence map›Paper›PMID 36467816›Full record

ArticleEJHaem2022

Risk-adjusted safety analysis of the oral JAK2/IRAK1 inhibitor pacritinib in patients with myelofibrosis.

Naveen Pemmaraju, Claire Harrison, Vikas Gupta, Srdan Verstovsek, Bart Scott, Stephen T Oh, Francesca Palandri, Haifa Kathrin Al-Ali, Marta Sobas, Mary Frances McMullin and 5 more

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 14 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

15 authors at 12 institutions in 6 countries.

Naveen PemmarajuThe University of Texas, MD Anderson Cancer Center Houston Texas USA.ORCID https://orcid.org/0000-0002-1670-6513
Claire HarrisonGuy's and St Thomas' NHS Foundation Trust London UK.
Vikas GuptaPrincess Margaret Cancer Centre University Health Network Toronto Ontario Canada.
Srdan VerstovsekThe University of Texas, MD Anderson Cancer Center Houston Texas USA.
Bart ScottFred Hutchinson Cancer Research Center Seattle Washington USA.
Stephen T OhWashington University School of Medicine St Louis Missouri USA.
Francesca PalandriIRCCS Azienda Ospedaliero-Universitaria di Bologna Istituto di Ematologia "Seràgnoli" Bologna Italy.
Haifa Kathrin Al-AliKrukenberg Cancer Center Halle University Hospital Halle Halle Germany.
Marta SobasDepartment of Hematology, Blood Neoplasms and Bone Marrow Transplantation Wroclaw Medical University Wrocław Poland.
Mary Frances McMullinQueen's University Belfast Belfast UK.
Ruben MesaUT Health San Antonio MD Anderson Cancer Center San Antonio Texas USA.
Sarah BuckleyCTI BioPharma Seattle Washington USA.
Karisse Roman-TorresCTI BioPharma Seattle Washington USA.
Alessandro VannucchiUniversity of Florence, Azienda Ospedaliera Universitaria Careggi Florence Italy.
Abdulraheem YacoubThe University of Kansas Cancer Center Westwood Kansas USA.
The University of Texas MD Anderson Cancer Center · USCTI BioPharma (United States) · USAzienda Ospedaliero-Universitaria Careggi · ITFred Hutch Cancer Center · USGuy's and St Thomas' NHS Foundation Trust · GBIstituto di Ematologia di Bologna · ITQueen's University Belfast · GBThe University of Kansas Cancer Center · USUniversity Health Network · CAUniversity Hospital in Halle · DEWashington University in St. Louis · USWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The safety profile of the novel oral JAK2/IRAK1 inhibitor pacritinib in patients with cytopenic myelofibrosis was described in the Phase 2 PAC203 and Phase 3 PERSIST-2 studies. To account for longer treatment durations on the pacritinib arms compared to best available therapy (BAT), we present a risk-adjusted safety analysis of event rates accounting for different time on treatment. While the rate of overall events was higher on pacritinib compared to BAT, the rate of fatal events was lower, and there was no excess in bleeding, cardiac events, secondary malignancy, or thrombosis on pacritinib, including in patients with severe thrombocytopenia.

Indexed as

myelofibrosismyeloproliferative neoplasmspacritinibsafety

Identifiers

PMID36467816
PMCPMC9713029
OpenAlexW4306921860

What OpenQuestion holds

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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.