Evidence map›Paper›PMID 25545244›Full record

Trial reportAmerican journal of hematology2015

Molecular responses and chromosomal aberrations in patients with polycythemia vera treated with peg-proline-interferon alpha-2b.

Nicole C C Them, Klaudia Bagienski, Tiina Berg, Bettina Gisslinger, Martin Schalling, Doris Chen, Veronika Buxhofer-Ausch, Josef Thaler, Ernst Schloegl, Guenther A Gastl and 11 more

Open access · hybridAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in American journal of hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 3 syntheses or guidelines pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  6. Mathematical modeling ofProceedings of the National Academy of Sciences of the United States of America · 2026
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  19. Novel therapeutics in myeloproliferative neoplasms.Journal of hematology & oncology · 2020
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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

21 authors at 9 institutions in 2 countries.

Nicole C C ThemCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Klaudia Bagienski
Tiina Berg
Bettina Gisslinger
Martin Schalling
Doris Chen
Veronika Buxhofer-Ausch
Josef Thaler
Ernst Schloegl
Guenther A Gastl
Dominik Wolf
Karin Strecker
Alexander Egle
Thomas Melchardt
Sonja Burgstaller
Ella Willenbacher
Oleh Zagrijtschuk
Christoph Klade
Richard Greil
Heinz Gisslinger
Robert Kralovics
CeMM Research Center for Molecular Medicine · ATMedical University of Vienna · ATParacelsus Medical University · ATAOP Orphan (Austria) · ATDonauspital · ATInnsbruck Medical University · ATKlinikum Wels-Grieskirchen · ATHanusch Hospital · ATUniversity Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fifty-one polycythemia vera (PV) patients were enrolled in the phase I/II clinical study PEGINVERA to receive a new formulation of pegylated interferon alpha (peg-proline-IFNα-2b, AOP2014/P1101). Peg-proline-IFNα-2b treatment led to high response rates on both hematologic and molecular levels. Hematologic and molecular responses were achieved for 46 and 18 patients (90 and 35% of the whole cohort), respectively. Although interferon alpha (IFNα) is known to be an effective antineoplastic therapy for a long time, it is currently not well understood which genetic alterations influence therapeutic outcomes. Apart from somatic changes in specific genes, large chromosomal aberrations could impact responses to IFNα. Therefore, we evaluated the interplay of cytogenetic changes and IFNα responses in the PEGINVERA cohort. We performed high-resolution SNP microarrays to analyze chromosomal aberrations prior and during peg-proline-IFNα-2b therapy. Similar numbers and types of chromosomal aberrations in responding and non-responding patients were observed, suggesting that peg-proline-IFNα-2b responses are achieved independently of chromosomal aberrations. Furthermore, complete cytogenetic remissions were accomplished in three patients, of which two showed more than one chromosomal aberration. These results imply that peg-proline-IFNα-2b therapy is an effective drug for PV patients, possibly including patients with complex cytogenetic changes.

Indexed as

Chromosome AberrationsPolymorphism, Single NucleotideAdultAgedAged, 80 and overAntineoplastic AgentsCohort StudiesDNAFemaleGene FrequencyGenome-Wide Association StudyHumansInterferon-alphaInterferon alpha-2Janus Kinase 2MaleAntineoplastic AgentsDNAInterferon-alphaInterferon alpha-2JAK2 protein, humanJanus Kinase 2peginterferon alfa-2bPolyethylene GlycolsRecombinant Proteins

Identifiers

PMID25545244
PMCPMC4657499
OpenAlexW1547986283

What OpenQuestion 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 OpenQuestion graph.