Evidence map›Paper›PMID 39804351›Full record

ArticleAnnals of hematology2025

PARADIGM-PV: a randomized, multicenter phase 4 study to assess the efficacy and safety of ropeginterferon alfa-2b in patients with low- or high-risk polycythemia vera.

Abdulraheem Yacoub, Ghaith Abu-Zeinah, Albert Qin, Tsewang Tashi, Waleed Da'na, Weichung Joe Shih, Oleh Zagrijtschuk, Chan-Yen Tsai, Robert Geller, Norio Komatsu and 2 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. 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

12 authors.

Abdulraheem YacoubHematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas, MO, USA. ayacoub@kumc.edu.
Ghaith Abu-ZeinahDivision of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY, 10021, USA.
Albert QinPharmaEssentia Corporation, Taipei, Taiwan.
Tsewang TashiHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Waleed Da'naKing Hussein Cancer Center, Amman, Jordan.
Weichung Joe ShihRutgers University School of Public Health, Piscataway, NJ, USA.
Oleh ZagrijtschukPharmaEssentia USA, Burlington, MA, USA.
Chan-Yen TsaiKing Hussein Cancer Center, Amman, Jordan.
Robert GellerPharmaEssentia USA, Burlington, MA, USA.
Norio KomatsuPharmaEssentia Japan K.K, Akasaka Center Building 12 F, Minato-Ku, Tokyo, 107-0051, Japan.
Ruben MesaAtrium Health, Levine Cancer Institute, Wake Forest University School of Medicine, Cancer Programs, Charlotte, NC, USA.
Harinder GillDepartment of Medicine, School of Clinical Medicine, LKS Faculty of Medicine, the University of Hong Kong, Hong Kong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycythemia vera (PV) is characterized by clonal hematopoietic stem or progenitor cells with constitutively active somatic mutation(s) in the Janus kinase 2 gene. Phlebotomy (Phl) and aspirin are often used alone for low-risk PV patients. However, data from the Low-PV study demonstrated that Phl and aspirin may not be adequate for patients. Therapeutic intervention with disease-modifying treatment appears to be beneficial for patients with PV regardless of the risk category. Ropeginterferon alfa-2b (ropeg) is a novel interferon-based therapy with favorable dosing schedules. A higher starting-dose (250 µg) regimen with simpler dose titrations was found to have a potent disease-modifying effect with respect to inducing a molecular response. PARADIGM-PV is a randomized, phase 4 study with the primary goal of assessing the efficacy of ropeg at this dosing regimen in alleviating Phl-dependence in both low- and high-risk patients with PV. The secondary endpoints include complete hematologic response, molecular response, symptom improvement, maintenance of median hematocrit (Hct) values < 45% without disease progression, and safety. Patients will be randomized equally to receive either ropeg every two weeks or to continue their current treatment with Phl or other cytoreductive agents (e.g., hydroxyurea, other interferons, or ruxolitinib) as applicable. All patients will receive Phl if their Hct values are elevated to ≥45% according to the National Comprehensive Cancer Network guidelines. The study will enroll approximately 70 patients internationally, including patients in the US. This study will provide new efficacy data, measured as the ability of ropeg to reduce Phl eligibility and modify the disease.

Indexed as

Interferon-alphaPolycythemia VeraPolyethylene GlycolsAdultAgedClinical Trials, Phase IV as TopicFemaleHumansInterferon alpha-2Janus Kinase 2MaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicRecombinant ProteinsTreatment OutcomeInterferon-alphaInterferon alpha-2JAK2 protein, humanJanus Kinase 2peginterferon alfa-2bPolyethylene GlycolsRecombinant ProteinsDisease-modifyingDisease progressionLow- and high-risk PVPhlebotomyPolycythemia vera (PV)Ropeginterferon alfa-2b

Identifiers

PMID39804351
PMCPMC11868303

What Socratic holds

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Registered trials

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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 Socratic graph.