Evidence map›Paper›PMID 21389325›Full record

ReviewBlood2011

The renaissance of interferon therapy for the treatment of myeloid malignancies.

Jean-Jacques Kiladjian, Ruben A Mesa, Ronald Hoffman

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03003325 (The Benefit/Risk Profile of Pegylated Proline-Interferon Alpha-2b), which is not on this map. Cited by 79 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 3 pooled it
13.5field-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.

NCT03003325 phase2completednot on this mapstarted 2017, after this paper: background citation

The Benefit/Risk Profile of Pegylated Proline-Interferon Alpha-2b (AOP2014) Added to the Best Available Strategy Based on Phlebotomies in Low-risk Patients With Polycythemia Vera (PV). The Low-PV Randomized Trial

TypeinterventionalSponsorFROM- Fondazione per la Ricerca Ospedale di Bergamo- ETSRan2017 to 2023Enrolled127ConditionsPolycythemia VeraArmsAOP2014, Phlebotomies, ASA
3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 3 syntheses or guidelines pooled it, 206 citations in OpenAlex.

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  19. Interferons in the treatment of myeloproliferative neoplasms.Therapeutic advances in hematology · 2024
    Review
  20. Article

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

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

3 authors at 3 institutions in 2 countries.

Jean-Jacques KiladjianHôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris, France. jean-jacques.kiladjian@sls.aphp.fr
Ruben A Mesa
Ronald Hoffman
Assistance Publique – Hôpitaux de Paris · FRIcahn School of Medicine at Mount Sinai · USMayo Clinic in Arizona · US

Funding

Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
NCI NIH HHS P01 CA108671
6 · The paper itself

Abstract

IFNα has been used to treat malignant and viral disorders for more than 25 years. Its efficacy is likely the consequence of its broad range of biologic activities, including direct effects on malignant cells, enhancement of anti-tumor immune responses, induction of proapoptotic genes, inhibition of angiogenesis, and promotion of the cycling of dormant malignant stem cells. Because of the recent development of "targeted" therapies, the use of IFN has been dramatically reduced over the last decade. The increasing awareness of the multistep pathogenesis of many malignancies has suggested, however, that such an approach using target-specific agents is not universally effective. These observations have resulted in a number of recent clinical trials utilizing IFNα in patients with chronic myeloid leukemia (CML), systemic mast cell disease, hypereosinophilic syndrome and the Philadelphia chromosome-negative myeloproliferative neoplasms (MPN) with promising outcomes. These reports provide evidence that IFNα, alone or in combination with other agents, can induce surprisingly robust molecular response rates and possibly improve survival. Although IFNα at present remains an experimental form of therapy for patients with myeloid malignancies, these promising results suggest that it may become again an important component of the therapeutic arsenal for this group of hematologic malignancies.

Indexed as

ApoptosisBenzamidesCell ProliferationClinical Trials as TopicHematologic NeoplasmsHematopoietic Stem CellsHumansHypereosinophilic SyndromeImatinib MesylateInterferon Type ILeukemia, MyeloidMastocytosisNeoplastic Stem CellsNeovascularization, PathologicPiperazinesPolycythemia VeraBenzamidesImatinib MesylateInterferon Type IPiperazinesPyrimidinesRecombinant Proteins

Identifiers

PMID21389325
PMCPMC12794401
OpenAlexW2024706907

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.