Evidence map›Paper›PMID 33012187›Full record

ArticleExpert review of hematology2020

Developing strategies to reduce the duration of therapy for patients with myeloproliferative neoplasms.

Michal Bar-Natan, Ronald Hoffman

Open access · greenAbstract read
In one paragraph

Article in Expert review of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 87% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Interferons in the treatment of myeloproliferative neoplasms.Therapeutic advances in hematology · 2024
    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

2 authors at 1 institution in 1 country.

Michal Bar-NatanIcahn School of Medicine at Mount Sinai Hospital, Tisch Cancer Institute , New York, NY, USA.
Ronald HoffmanIcahn School of Medicine at Mount Sinai Hospital, Tisch Cancer Institute , New York, NY, USA.
Mount Sinai Hospital · US

Funding

Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
TARGETING RETROVIRAL VECTORS TO HEMATOPOIETIC STEM CELLSP01HL053762 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KAN, YUET W · 1994 to 2004
$5.1M
NCI NIH HHS P01 CA108671NHLBI NIH HHS P01 HL053762
6 · The paper itself

Abstract

introductionAll current treatment strategies for myeloproliferative neoplasms (MPN) patients with the exception of allogeneic stem cell transplant (ASCT) are continuously administered. Treatment approaches that reduce the degree of minimal residual disease (MRD) might permit possible drug holidays or potential cures. AREA COVERED: Authors discuss the presently available agents and those that are under clinical development that might induce a state of MRD and can be administered intermittently. Data extracted from a comprehensive search of peer review literature performed in Pubmed as well as information presented in scientific meetings. EXPERT OPINION: Currently, the only potential curative treatment for MPN is ASCT. ASCT requires a period of intense treatment but ultimately allows the patient to enjoy a period independent of continued treatment. There is evidence that intermittent use of busulfan or prolonged use of IFN-α can induce hematological remissions that are sustained for prolonged periods of time, allowing for drug holidays. The experimental drug Imetelstat is a promising drug that has been reported to prolong survival in very high-risk myelofibrosis patients after a limited period of time of administration. New experimental drugs and drug combinations that target the malignant clone and/or microenvironmental abnormalities have the potential to eliminate MRD, which might allow for drug holidays and reduction in the duration of therapy.

Indexed as

Duration of TherapyAllograftsAntineoplastic Agents, AlkylatingClinical Trials as TopicCombined Modality TherapyDisease ManagementDrug Administration ScheduleDrugs, InvestigationalDrug Therapy, CombinationHematinicsHematopoietic Stem Cell TransplantationHormonesHumansImmunologic FactorsInterferon-alphaMyeloproliferative DisordersAntineoplastic Agents, AlkylatingDrugs, InvestigationalHematinicsHormonesimetelstatImmunologic FactorsInterferon-alphaOligonucleotidesTelomeraseASCTbusulfanimetelestatinterferon-αMPN

Identifiers

PMID33012187
PMCPMC8691658
OpenAlexW3090484391

What OpenQuestion holds

Textmetadata
LicenceTDM
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.