Evidence map›Paper›PMID 31991066›Full record

ArticleCancer medicine2020

Data-driven analysis of JAK2V617F kinetics during interferon-alpha2 treatment of patients with polycythemia vera and related neoplasms.

Rasmus K Pedersen, Morten Andersen, Trine A Knudsen, Zamra Sajid, Johanne Gudmand-Hoeyer, Marc J B Dam, Vibe Skov, Lasse Kjaer, Christina Ellervik, Thomas S Larsen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  17. The Combination ofCancer control : journal of the Moffitt Cancer Center
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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

14 authors at 4 institutions in 2 countries.

Rasmus K PedersenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0001-5946-8220
Morten AndersenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0001-7582-0685
Trine A KnudsenDepartment of Haematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0001-9829-3099
Zamra SajidDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-9143-3092
Johanne Gudmand-HoeyerDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-4972-0653
Marc J B DamDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0003-0096-9690
Vibe SkovDepartment of Haematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0003-0097-7826
Lasse KjaerDepartment of Haematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0001-6767-0226
Christina EllervikDepartment of Production, Research, and Innovation, Region Zealand, Sorø, Denmark.ORCID 0000-0002-3088-4375
Thomas S LarsenDepartment of Hematology, Odense University Hospital, Odense, Denmark.ORCID 0000-0002-8418-6708
Dennis HansenDepartment of Hematology, Odense University Hospital, Odense, Denmark.ORCID 0000-0002-4478-1297
Niels PallisgaardDepartment of Surgical Pathology, Zealand University Hospital, Roskilde, Denmark.
Hans C HasselbalchDepartment of Haematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0003-3936-8032
Johnny T OttesenDepartment of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-9786-0300
Roskilde University · DKZealand University Hospital · DKOdense University Hospital · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment with PEGylated interferon-alpha2 (IFN) of patients with essential thrombocythemia and polycythemia vera induces major molecular remissions with a reduction in the JAK2V617F allele burden to undetectable levels in a subset of patients. A favorable response to IFN has been argued to depend upon the tumor burden, implying that institution of treatment with IFN should be as early as possible after the diagnosis. However, evidence for this statement is not available. We present a thorough analysis of unique serial JAK2V617F measurements in 66 IFN-treated patients and in 6 untreated patients. Without IFN treatment, the JAK2V617F allele burden increased exponentially with a period of doubling of 1.4 year. During monotherapy with IFN, the JAK2V617F allele burden decreased mono- or bi-exponentially for 33 responders of which 28 patients satisfied both descriptions. Bi-exponential description improved the fits in 19 cases being associated with late JAK2V617F responses. The decay of the JAK2V617F allele burden during IFN treatment was estimated to have half-lives of 1.6 year for the monoexponential response and 1.0 year in the long term for the bi-exponential response. In conclusion, through data-driven analysis of the JAK2V617F allele burden, we provide novel information regarding the JAK2V617F kinetics during IFN-treatment, arguing for early intervention.

Indexed as

AdultAgedAllelesFemaleHumansInterferon-alphaInterferon alpha-2Janus Kinase 2MaleMiddle AgedPolycythemia VeraPolyethylene GlycolsPolymorphism, Single NucleotidePrimary MyelofibrosisProspective StudiesReal-Time Polymerase Chain ReactionInterferon-alphaInterferon alpha-2JAK2 protein, humanJanus Kinase 2peginterferon alfa-2apeginterferon alfa-2bPolyethylene GlycolsRecombinant Proteinsearly treatmentessential thrombocythemiainterferon-alpha2JAK2V617F kineticsmyeloproliferative neoplasmspolycythemia veraprimary myelofibrosis

Identifiers

PMID31991066
PMCPMC7064092
OpenAlexW3004067129

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.