Evidence map›Paper›PMID 31515250›Full record

Trial reportBlood2019

Pegylated interferon alfa-2a for polycythemia vera or essential thrombocythemia resistant or intolerant to hydroxyurea.

Abdulraheem Yacoub, John Mascarenhas, Heidi Kosiorek, Josef T Prchal, Dmitry Berenzon, Maria R Baer, Ellen Ritchie, Richard T Silver, Craig Kessler, Elliott Winton and 24 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01259856 (Randomized Trial of Pegylated Interferon Alfa-2a Versus Hydroxyurea Therapy in the Treatment of High Risk Polycythemia Vera), which is not on this map. Cited by 98 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 6 pooled it
14.4field-weighted citation impact, top 1% 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.

NCT01259856 phase3completednot on this map

Randomized Trial of Pegylated Interferon Alfa-2a Versus Hydroxyurea Therapy in the Treatment of High Risk Polycythemia Vera (PV) and High Risk Essential Thrombocythemia (ET)

TypeinterventionalSponsorRonald HoffmanRan2011 to 2017Enrolled168ConditionsHigh Risk Polycythemia Vera, High Risk Essential ThrombocythemiaArmsPEGASYS, Hydroxyurea, Aspirin
3 · Its place in the literature

Who cites it

98 citing papers in PubMed, 6 syntheses or guidelines pooled it, 166 citations in OpenAlex.

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38 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 20 institutions in 2 countries.

Abdulraheem YacoubDivision of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas Cancer Center, Westwood, KS.
John MascarenhasTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Heidi KosiorekMayo Clinic, Scottsdale, AZ.
Josef T PrchalDivision of Hematology, University of Utah School of Medicine and.
Dmitry BerenzonComprehensive Cancer Center, Wake Forest University Medical Center, Wake Forest Health, Winston-Salem, NC.
Maria R BaerGreenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD.
Ellen RitchieDivision of Hematology and Oncology, Department of Medicine, Richard T. Silver Myeloproliferative Neoplasms Center, Weill Cornell Medical College, New York, NY.
Richard T SilverDivision of Hematology and Oncology, Department of Medicine, Richard T. Silver Myeloproliferative Neoplasms Center, Weill Cornell Medical College, New York, NY.
Craig KesslerGeorgetown University Medical Center, Washington, DC.
Elliott WintonWinship Cancer Institute, Emory University School of Medicine, Atlanta, GA.
Maria Chiara FinazziDepartment of Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Alessandro RambaldiDepartment of Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Alessandro M VannucchiCenter for Research and Innovation of Myeloproliferative Neoplasms, Azienda Ospedaliero-Universitaria Careggi, and.
David LeibowitzDepartment of Oncology, Palo Alto Medical Foundation, Sutter Health, Palo Alto, CA.
Damiano RondelliDivision of Hematology and Oncology, University of Illinois, Chicago, IL.
Murat O ArcasoyDivision of Hematology, Duke University School of Medicine, Durham, NC.
Rosalind CatchatourianDepartment of Oncology, John H. Stroger Jr. Hospital of Cook County, Chicago, IL.
Joseph VadakaraGeisinger Medical Center, Danville, PA.
Vittorio RostiLaboratory of Biochemistry, Biotechnology, and Advanced Diagnosis, Center for the Study of Myelofibrosis, Istituto Di Ricovero e Cura a Carattere Scientifico, Foundation Policlinico San Matteo, Pavia, Italy.
Elizabeth HexnerAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Marina KremyanskayaTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Lonette SandyTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Joseph TripodiDepartment of Pathology and.
Vesna NajfeldDepartment of Pathology and.
Noushin FarnoudHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Elli PapaemmanuilComputational Oncology.
Mohamed SalamaMayo Clinic Laboratories, Rochester, MN.
Rona Singer-WeinbergNew York Blood Center, New York, NY.
Raajit RampalHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
Judith D GoldbergDepartment of Population Health and.
Tiziano BarbuiOspedali Riuniti, Bergamo, Italy; and.
Ruben MesaUT Health San Antonio Cancer Center, San Antonio, TX.
Amylou C DueckMayo Clinic, Scottsdale, AZ.
Ronald HoffmanTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Icahn School of Medicine at Mount Sinai · USMemorial Sloan Kettering Cancer Center · USCornell University · USMayo Clinic in Arizona · USAzienda Ospedaliero-Universitaria Careggi · ITAzienda Ospedaliero Universitaria Ospedali Riuniti · ITDuke University · USEmory University · USGeisinger Medical Center · USGeorgetown University · USHuntsman (United States) · USJohn H. Stroger, Jr. Hospital of Cook County · USMayo Clinic · USNew York Blood Center · USNew York University · USOspedale Papa Giovanni XXIII · ITSutter Health · USThe University of Kansas Cancer Center · USThe University of Texas Health Science Center at San Antonio · USUniversity Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
TARGETING RETROVIRAL VECTORS TO HEMATOPOIETIC STEM CELLSP01HL053762 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KAN, YUET W · 1994 to 2004
$5.1M
Genomic profiling and development of murine models of transformation of MPNsK08CA188529 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI RAMPAL, RAAJIT · 2014 to 2018
$891k
NCI NIH HHS K08 CA188529NCI NIH HHS P01 CA108671NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA054174NHLBI NIH HHS P01 HL053762
6 · The paper itself

Abstract

Prior studies have reported high response rates with recombinant interferon-α (rIFN-α) therapy in patients with essential thrombocythemia (ET) and polycythemia vera (PV). To further define the role of rIFN-α, we investigated the outcomes of pegylated-rIFN-α2a (PEG) therapy in ET and PV patients previously treated with hydroxyurea (HU). The Myeloproliferative Disorders Research Consortium (MPD-RC)-111 study was an investigator-initiated, international, multicenter, phase 2 trial evaluating the ability of PEG therapy to induce complete (CR) and partial (PR) hematologic responses in patients with high-risk ET or PV who were either refractory or intolerant to HU. The study included 65 patients with ET and 50 patients with PV. The overall response rates (ORRs; CR/PR) at 12 months were 69.2% (43.1% and 26.2%) in ET patients and 60% (22% and 38%) in PV patients. CR rates were higher in CALR-mutated ET patients (56.5% vs 28.0%; P = .01), compared with those in subjects lacking a CALR mutation. The median absolute reduction in JAK2V617F variant allele fraction was -6% (range, -84% to 47%) in patients achieving a CR vs +4% (range, -18% to 56%) in patients with PR or nonresponse (NR). Therapy was associated with a significant rate of adverse events (AEs); most were manageable, and PEG discontinuation related to AEs occurred in only 13.9% of subjects. We conclude that PEG is an effective therapy for patients with ET or PV who were previously refractory and/or intolerant of HU. This trial was registered at www.clinicaltrials.gov as #NCT01259856.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsDrug Resistance, NeoplasmFemaleHumansHydroxyureaInterferon-alphaMaleMiddle AgedPolycythemia VeraPolyethylene GlycolsRecombinant ProteinsThrombocythemia, EssentialTreatment OutcomeAntineoplastic AgentsHydroxyureaInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsRecombinant Proteins

Identifiers

PMID31515250
PMCPMC6839950
OpenAlexW2972422263

What OpenQuestion holds

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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.